Targets for protection and mitigation of radiation injury

Abstract

Protection of normal tissues against toxic effects of ionizing radiation is a critical issue in clinical and environmental radiobiology. Investigations in recent decades have suggested potential targets that are involved in the protection against radiation-induced damages to normal tissues and can be proposed for mitigation of radiation injury. Emerging evidences have been shown to be in contrast to an old dogma in radiation biology; a major amount of reactive oxygen species (ROS) production and cell toxicity occur during some hours to years after exposure to ionizing radiation. This can be attributed to upregulation of inflammatory and fibrosis mediators, epigenetic changes and disruption of the normal metabolism of oxygen. In the current review, we explain the cellular and molecular changes following exposure of normal tissues to ionizing radiation. Furthermore, we review potential targets that can be proposed for protection and mitigation of radiation toxicity.

Introduction

For many years, it has been known that the use of free radical scavengers immediately before exposure to radiation can alleviate DNA damage and cell death. Further research has led to a large number of experimental studies defining appropriate radioprotectors. Investigations at the United States (US) Army Walter Reed Institute (Washington, DC) during the cold war led to the development of a potent drug with high radioprotection efficiency, named WR2721 or amifostine [1]. This compound is a sulfhydryl containing agents that interact and neutralize free radicals [2]. Afterwards, other agents containing sulfhydryl groups were developed to reduce oxidative stress and radiation toxicity. N-Acetylcysteine and captopril are sulfhydryl agents that have been used for radioprotection in some experimental studies [3]. Although amifostine has been used as a radiation modifier in clinical trials, some studies have reported severe toxicities which led to its use being discontinued [4]. In clinical studies, amifostine has been commonly used for head and neck cancer radiotherapy for reducing xerostomia [5].

To date, several agents have been investigated for use as a radioprotector, with some chemical and natural agents showing effective radioprotection. However, the efficiency of each radioprotector could be limited to some organs/tissues [6]. Moreover, for the protection of normal tissues in radiotherapy, it is crucial to consider possible effects on tumor response [7]. For the protection of a particular organ, we need to choose the best agent, which may be different from those used for other organs [8].

In recent decades, several studies have been conducted to protect and mitigate radiation toxicity using some supplements after exposure to radiation. In addition to clinical applications, radiation mitigators can be used to reduce mortality and normal tissue toxicity after an accidental nuclear or radiological disaster [9]. Radiation mitigators are mostly for the bone marrows and gastrointestinal system injury; however, studies have suggested that mitigators can be used to alleviate radiation toxicity in the lung, heart and kidney [10]. Acute damages to the bone marrows and gastrointestinal system may lead to death some days to weeks following whole-body exposure to radiation. However, in some cases, following local abdomen and chest exposure or non-homogenous whole-body exposure to radiation, the incidence of lung pneumonitis, cardiopulmonary fibrosis or nephropathy may cause death some months to years later [11]. Total body irradiation (TBI) for patients with leukemia may also lead to pneumonitis and nephropathy [12]. Investigations into the development of new agents with high efficiency for mitigation and protection of radiosensitive organs are ongoing. In the current paper, we review recent advances in the mitigation of radiation toxicity and also suggest promising strategies for preventing mortality and side effects that affect the quality of life of exposed people.

Promising targets for radiation protection and mitigation

Emerging evidences indicate that in addition to radiation dose, normal tissue toxicity is highly dependent on hierarchical events that occur in cells after irradiation. At the first level, DNA damage response (DDR) determines cell death or repair of DNA. DDR is initiated some minutes to hours after exposure to radiation [13]. Enhancing DNA repair capacity has been proposed for ameliorating DNA damage and reducing cell death [14]. If damages to the DNA are not completely repaired, oxidized DNA or cell contents from dying cells trigger activation of several signaling pathways that play a pivotal role in the incidence of radiation injury [13]. Cell death through apoptosis, necrosis, autophagy or senescence induces the activation of inflammatory mediators and pro-oxidant enzymes [15–17]. It seems that DNA repair enzymes and cell death pathways are activated from the first minutes to hours after exposure to radiation; however, ROS/NO generating enzymes are upregulated after some hours to weeks [18]. The expression of inflammatory and pro-oxidant mediators is time-dependent and tissue-specific. Furthermore, the quality and quantity of their expressions vary for different organs. Thus, it seems that the efficiency of a radiation protector or mitigator is highly dependent on the time of administration as well as irradiated organs [19]. In this review, the potential targets for the amelioration of radiation toxicity in different organs will be discussed. These targets can be proposed for both protection and mitigation of radiation injury for clinical radiotherapy and also for radiological and nuclear disasters.

Targeting cell death after exposure to ionizing radiation

Radiation-induced cell death is the consequence of massive DNA damage and accumulation of unrepaired chromosome breaks. Mitotic catastrophe is a non-immunogenic type of cell death and does not trigger inflammatory or tolerogenic responses. Autophagy also does not play a major role in the side effects of ionizing radiation. Other types of cell death including necrosis, apoptosis and senescence lead to some changes in the response of immune system and reduction/oxidation (redox) reaction that is associated with the appearance of oxidative stress and inflammation [18, 20]. Necrosis usually occurs following massive injury to the membrane, DNA, mitochondria and other organelles within cells. This may be observed some hours after irradiation [21]. Apoptosis and senescence are two important types of cell death that occur following the upregulation and downregulation of some genes that are involved in the progression of death or survival [22]. Modulation of these types of cell death can be suggested as potential strategies for mitigation of radiation injury. This can increase the survival of radiosensitive cells in bone marrow and small intestine thus helps mitigate radiation-induced mortality.

Apoptosis

Apoptosis is the main mechanism of cell death in highly radiosensitive organs such as the bone marrow, gastrointestinal system, testis and skin [23, 24]. High incidence of apoptosis in these organs lead to severe damage to the normal function of organs, leading to the appearance of severe reactions and consequences for exposed people. Apoptosis occurs following DNA damage and increases the release of some cell death signals such as Fas, TNF-α and TGF-β, as well as increased activity of p53 [23]. Each of these mediators via binding to their receptors initiates apoptosis signaling pathways. TGF-β via binding to TGFβR1 or TGFβR2 causes activation of pro-apoptosis Bax via Smad2/3 pathway. Fas binds to Fas ligand (FasL or CD95L); however, TNF-α can bind to TNF receptor (TNFR) or TRAIL. Upregulation of FasL, TNFR or TRAIL cause stimulation of caspase-8 and caspase-10 to induce activation and penetration of Bax into the mitochondria [25]. Upregulation of TNFR and also the production of free radicals after exposure of membrane to ionizing radiation can stimulate the development of ceramide, which suppresses Bcl-2, an inhibitor of pro-apoptosis Bax. Penetration of Bax into the mitochondria leads to the release of cytochrome C. Usually, early apoptosis occurs following damage to mitochondria and release of cytochrome C. This is followed by interaction of cytochrome C with Apaf1 and caspase-9 and the development of apoptosome complex. This complex is able to degrade DNA and other macromolecules such as the membrane, leading to the development of apoptotic bodies [26]. Some mediators such as NF-κB or PI3K can suppress the progression of apoptosis via upregulation of Bcl-2 [27] (Fig. 1).

Fig. 1.

Apoptosis pathways after exposure to ionizing radiation. Exogenous and endogenous ROS trigger upregulation of apoptosis receptors which cause Bax upregulation and downregulation of Bcl-2. DNA damage and p53 also have key roles in the initiation of apoptosis signaling pathways. Apoptosis clearance by macrophages leads to their activation and is associated with NO generation. NO can interact with Ogg1, a key player in BER pathway, thus suppresses DDR. Neutralization of NO can boost DDR, thus reduces apoptosis. Furthermore, activation of TLR4&5 can increase the expression of NF-κB, leading to inhibition of Bax and upregulation of Bcl-2. P38 has a negative role and its suppression can preserve cell viability

To date, few studies have tried to inhibit apoptosis and improve normal tissue tolerability using selective anti-apoptotic inhibitors. Targeting TGF-β in mice model has been shown to attenuate radiation-induced bone marrow injury. However, there is a possibility that the suppression of TGF-β reduces apoptosis following attenuation of ROS generating enzymes and mitochondrial-derived superoxide suppression [28]. The intestine is another highly radiosensitive organ because of the high incidence of apoptosis in progenitor stem cells. Apoptosis in these cells leads to shortening of villi and crypt. Crypt and villi require permanent turnover by mitosis in intestinal stem cells. In mice intestine, it has been shown that mitochondrial pathway is responsible for apoptosis following exposure to radiation. Inhibition of Bax or PUMA could improve intestinal recovery after exposure to 8 or 18 Gy radiation. Interestingly, PUMA knockdown in mice showed more protection compared to Bax knockdown in mice. Results indicated that PUMA via induction of apoptosis in intestinal progenitor cells plays a main role in radiation-induced intestinal injury in mice [29]. P53 also has a key role in the initiation of apoptosis signaling pathways in the intestine. Although it is a central regulator of DNA damage response, overexpression of p53 has been observed to be associated with increased apoptosis in the crypt [30].

Lymphocytes are one of the most radiosensitive cells. Lymphocytes do not have mitotic activity, while they have a bigger nucleus compared to other cells that may be involved in radiosensitization of lymphocytes. It has been suggested that high expressions of pro-apoptotic genes such as Bax, PUMA and p53 play a key role in the high incidence of apoptosis in lymphocytes. Furthermore, radiation may trigger ROS production by lymphocytes, thus increases the probability of DNA damage and apoptosis [31]. Treatment of lymphocytes with some agents has been shown to reduce the expression of pro-apoptotic genes such as Bax and increase the expression of anti-apoptotic Bcl-2 [32, 33]. Some other strategies have been proposed to mitigate radiation toxicity via inhibition of apoptosis initiation. Enhancing DNA repair capacity is an interesting idea. Furthermore, triggering anti-apoptotic genes such as toll-like receptors (TLRs) or suppression of pro-apoptotic genes such as p38 have shown interesting results. Inhibition of apoptosis is favor for normal tissues sparing, while, in cancer radiotherapy this strategy can reduce the effectiveness of therapy. Thus, apoptosis targeting is an appropriated strategy for radiation mitigation, but not for radiotherapy [34, 35].

Boosting DNA repair for preventing apoptosis

As earlier mentioned, unrepaired DNA damage is responsible for cell death through mitotic catastrophe, senescence and apoptosis. As apoptosis is responsible for the death of highly radiosensitive cells such as the bone marrow and small intestinal progenitor cells, it seems that boosting DNA repair capacity can help prevent cell death through apoptosis. Enoxacin is an agent that has been shown to increase the activity and facilitates faster DNA repair, thus causes more survival of irradiated cells. This agent is able to increase the number of 53BP1 to damaged DNA sites [36]. βarrestin-1 (βarr1) is another key player of DDR that has been linked to active p53 pathway. βarr1 is involved in the regulation of MMD2, a protein that causes degradation of p53. Thus, suppression of βarr1 can stimulate p53 activity and enhance DDR, leading to reduction of radiation toxicity. It has been shown that βarr1 knockdown can increase p53 binding to damaged DNA sites [37].

One of the most important suppressive effects of ionizing radiation on DNA repair mechanisms is nitroacetylation of 8-oxoguanine glycosylase (Ogg1) following the generation of NO by inflammatory cells. Ogg1 is a key enzyme in base excision repair (BER) pathway and is responsible for removing 8-hydroxyguanine (8-oxoG), a product of ROS interaction with DNA. Activation of these enzymes after exposure to ionizing radiation can increase resistance to radiation-induced DNA damage [38]. Furthermore, the acetylation and turnover of Ogg1 by Sirt3 can amplify DNA repair in the mitochondria, thus protects against radiation-induced mitochondrial apoptosis [39].

p53

Although p53 plays a key role in DDR, activation of apoptosis pathway by it can increase radiosensitivity via depletion of stem/progenitor cells. For 2 decades ago, it has shown that suppression of p53 in combination with irradiation can increase the viability of mice C8 cells [40]. Thus, inhibition of p53 may attenuate massive apoptosis to mitigate radiation toxicity in high radiosensitive organs. A study suggested that p53 may have dual role depend on targeted organ. Knockdown of p53 has shown that can increase resistance to radiation-induced hematopoietic system injury, while its inhibition cause more damage to the repopulation of progenitor cells in intestinal epithelial cells [41]. In fact, mechanisms of radiosensitivity in bone marrow and intestine are different. A study showed that although p53 promotes apoptosis in bone marrow progenitor cells, it plays a key role in regulating cell cycle and mitosis in intestine epithelial cells. Targeting p53 can disrupt the regulation of cell cycle checkpoints, thus increase mitotic death of epithelial cells. This shows that p53 targeting increases the radiosensitivity of epithelial cell independent of apoptosis [42]. Pifithrin-mu is an inhibitor of p53 binding to mitochondria. Treatment of mouse thymocytes with pifithrin-mu can increase the viability and reduce apoptosis. Furthermore, administration of Pifithrin-mu has shown that increase survival following whole-body irradiation with lethal doses of ionizing radiation [43]. Sodium orthovanadate is another agent that has shown protect against ionizing radiation through blunting p53 interactions with Bcl-2 and mitochondria. This study suggested that complete radioprotection can be achieved when transcription-dependent and transcription-independent pathways of p53 inhibited [44]. A further study showed that sodium orthovanadate can suppress p53 dependent apoptosis, not p53 independent apoptosis [45].

P53 targeting with sodium orthovanadate also has shown that mitigate lethality of whole-body exposure to radiation. Evaluating different time points for the administration of sodium orthovanadate showed that the best time for mitigation of radiation-induced lethality is immediate after whole-body irradiation. this may indicate that p53 activate apoptosis immediately after exposure of bone marrow stem/progenitor cells to ionizing radiation [46]. Knockdown of p53 can mitigate radiation injury in brain too. In an animal study has shown that inhibition of p53 can attenuate defect in the irradiated brain in mice and help to the development of normal brain [47]. Zinc(II) chelators such as bis(2-pyridylmethyl)amine, tris(2-pyridylmethyl)amine, 1,4,7,10-tetraazacyclododecane, Bispicen, and TPEN are p53 inhibitors that also have shown can protect against radiation-induced apoptosis [48]. P53 has a key role in tumor response to radiation. For the protection of highly radiosensitive organs such as the intestines and bone marrow cells, we need to inhibit p53 without attenuating the responses of cancer cells. For targeting p53, we should consider the expression of p53 in cancer cells. It has been suggested that most solid tumors have mutant p53 [49]. In most conditions, mutant p53 leads to a loss in its function [50]. TP53 genetic test gives a better understanding of the genetic background of tumors for using p53 inhibitors during radiotherapy. In this condition, p53 targeting can be proposed for patients with mutant p53 for protection of normal tissues without adverse effect on tumor response to radiotherapy.

TLRs

TLRs are very critical receptors that mediate inflammatory responses to damage-associated molecular-pattern (DAMP) molecules. These receptors belong to pattern recognition receptors (PRRs) family. Some TLRs including TLR2, TLR4, TLR5, TLR6 and TLR9 which depend on HMGB1 are involved in the progression of inflammatory responses and immune system activation [51]. One of the main effects of TLRs is the induction of anti-apoptotic signaling pathways, which may be involved in the protection of radiosensitive cells to apoptosis [52]. Targeting TLRs using agonists has been shown to protect and mitigate radiation toxicity in normal tissues. In an animal study, Kurkjian et al. showed mitigation of acute radiation syndrome (ARS) following TLR2/6 targeting. Fibroblast-stimulating lipopeptide (FSL-1), an agonist of TLR2/6 administered 24 h after whole-body irradiation with a lethal dose of radiation showed 50% survival for 30 days. However, administration of other TLR agonists did not show any improvement in survival. FSL-1 could induce G-CFU, thus improved hematopoietic activity and increased number of peripheral blood cells [53].

Targeting TLR5 in an in vivo study showed interesting results for both protection and mitigation of radiation injury in highly radiosensitive organs, leading to increased survival. Whole-body exposure of mice to 13 Gy led to 100% mortality, while pre-irradiation treatment with TLR5 agonist caused 87% survival. Interestingly, treatment with TLR5 agonist even 1 h after irradiation led to 70% survival, thereby indicating the potent mitigatory effect of TLR5 agonist. In comparison to amifostine, which is the most common radioprotector, TLR5 agonist showed more efficiency [19]. TLR5 agonists may also help protect epithelial cells from toxic effects of ionizing radiation. Activation of TLR5 by CBLB502 (an optimized type of flagellin) showed protection of mice against radiation-induced dermatitis and mucositis. Interestingly, TLR5 agonist could reduce tumor volume following injection of A549. Similar results have been shown for Entolimod, another agonist of TLR5 [54].

Monophosphoryl lipid A (MPLA) is a TLR4 agonist that has shown radioprotective effect for both in vitro and in vivo models. MLPA triggers translocation of NF-κB and also increases the expression of MyD88, while it reduces the release of inflammatory cytokines. The levels of TNF-α and IL-6 were reduced, while that of IL-2 increased after MLPA administration. MLPA increases the number of nucleated cells and hematopoietic stem cells within the bone marrow. Treatment with MLPA reduced apoptosis in bone marrow cells, which may be due to the activation of NF-κB. Also, MLPA increased IFN-β (TRIF), which may be involved in its radioprotective effect [55]. CBLB502, a TLR5 agonist can also induce the release of IL-6 following NF-κB upregulation, leading to upregulation and activation of STAT-3. These changes suppress apoptosis and preserve progenitor stem cells [56]. Furthermore, TLR5 activation can stimulate the activation of NK cells, which kill cancer cells and inhibit metastasis [57]. It is suggested that upregulation of TLRs can induce maturation of dendritic cells, which activate immune system against cancer cells [58]. This property of TLRs can help to management of normal tissues toxicity by TLRs agonists without negative effect on tumor response to radiotherapy.

The role of TLRs in the development of radiation-induced diseases is complex and needs to be investigated for different organs. Although, TLRs can reduce apoptosis, their upregulation may be involved in the progression of inflammatory-related diseases that may appear in the long term after exposure to ionizing radiation [59]. A study showed that TLR4 knockdown in mice can ameliorate radiation-induced fibrosis in mice lung. Furthermore, TLR4 knockdown led to an improvement in hematopoietic system recovery [60]. In contrast, another study reported that knockdown of both TLR2 and TLR4 can amplify lung fibrosis [61]. Therefore, it seems that stimulation of TLRs is an interesting target for preventing ARS resulting from massive apoptosis in the bone marrow and intestine; however, caution should be observed for other organs.

TLRs agonists have shown interesting results for activation of the immune system against cancer cells. In combination with radiation, TLRs agonists have also shown promising results. However, it needs to be examined for each cancer type [62]. Studies suggested that upregulation of some TLRs like TLR4 is associated with shorter survival for different tumors, while others such as TLR5 upregulation predicts higher survival for lung cancer patients [63]. The main anti-tumor activity of TLRs is mediated through an increase in immune system’s activity like activation of cytotoxic T lymphocytes (CTLs) and triggering immunogenic functions of dendritic cells (DCs) and macrophages [64]. To date, some experimental studies have been conducted to investigate the roles of some TLRs agonists in combination with radiotherapy. Among the mentioned TLRs that can protect normal tissues, TLR7 and TLR9 have been investigated to determine the modulatory effects on tumor response to radiotherapy. CpG oligodeoxynucleotides, which activate TLR9 in DCs, can increase the response of implanted fibrosarcoma tumors in mice, thus increase tumor growth delay and survival in mice [65]. Administration of R848, a TLR7 agonist, in combination with radiotherapy has been shown to increase infiltration of CTLs in mice bearing lymphoma [66]. Similar studies indicated that activation of TLR7 leads to suppression of breast cancers, colorectal carcinoma, fibrosarcoma, colorectal and pancreatic cancers in mice via increasing infiltration of CTLs and NK cells, as well as the release of anti-tumor cytokines such as IFN-γ [67–69]. These results show that targeting some TLRs can act as radioprotector for normal tissues and also radiosensitizer for some tumors. For example, TLR5 and TLR7 stimulate the activities of anti-tumor CTLs and NK cells in tumor, while TLR5 suppresses apoptosis and TLR7 triggers the release of IFN-γ and stem cells’ proliferation in hematopoietic system [70]. TLR9 which has anti-tumor activity against fibrosarcoma, can also prevent apoptosis of irradiated cells and preserves the intestines [71].

p38 MAPK

MAPKs include some subfamilies including p38, extracellular signal-regulated kinases 1 and 2 (ERK1/2) as well as c-Jun amino-terminal kinases (JNKs) [72]. Among these subfamilies, p38 targeting has been investigated to ameliorate radiation-induced apoptosis. Inhibition of p38 has been shown to suppress upregulation of pro-apoptotic caspase-3 and PARP, thereby reducing apoptosis in auditory cells [73]. As p38 plays a key role in the promotion of apoptosis following exposure to ionizing radiation, some studies have investigated its targeting for mitigation of radiation toxicity in the bone marrow using p38 inhibition. Suppression of p38 by thioredoxin (TXN) has been shown to mitigate bone marrow hematopoietic stem cell death following exposure to radiation [74]. Inhibition of p38 in combination with granulocyte colony-stimulating factor (G-CSF) administration has also been suggested to improve the recovery of depleted bone marrow cells after exposure to radiation. This combination showed an increase in the number of hematopoietic stem/progenitor cells [75, 76]. Furthermore, inhibition of p38 enhances survival following administration of G-CSF; however, p38 inhibition when administered alone had no significant effect for mitigation of radiation mortality [77] (Fig. 1).

As p38 has a role in the initiation of apoptosis in several cancer cells, its inhibition may protect cancer cells against radiotherapy [78, 79]. Targeting p38 may be a useful candidate for radiation mitigation. However, its targeting during radiotherapy may be inappropriate and needs further elucidation for each cancer type.

Senescence

Senescence is a type of cell death that triggers inflammatory responses [80]. Senescence can occur in different such as fibroblasts, endothelial cells, epithelial cells, astrocytes etc. [81]. It has been suggested that senescence in fibroblasts following exposure to radiation can trigger fibrosis [82]. Clearance of senescent cells can reduce fibrosis and attenuate upregulation of fibrotic markers such as TGF-β [82]. It seems that DNA damage responses (DDRs) after exposure to radiation is responsible for the induction of senescence following upregulation of inflammatory mediators and release of a wide range of cytokines such as IL-1, IL-6, IL-8 and TGF-β [83]. P53 also has a role in senescence [84]. As p53 plays a central role in DDRs following exposure of cells to ionizing radiation, it is predictable that it plays a key role in senescence after irradiation. p53 knockdown has been shown to reduce senescence in irradiated cells [85]. Plasminogen activator inhibitor-1 (PAI-1) is another protein that plays a key role in the development of senescence [86]. It has been suggested that PAI-1 is downstream of TGF-β for inducing senescence [87]. PAI-1 knockdown is associated with increased survival after whole-body irradiation [88]. In fact, PAI-1 expression may predict the severity of radiation toxicity in some radiosensitive organs like intestine [88–90]. Chung et al. evaluated the role of PAI-1 in radiation-induced senescence and pulmonary fibrosis. They showed that pre and post-irradiation administration of rPAI-1₂₃ (truncated plasminogen activator inhibitor-1) can prevent fibrosis in mice lung. The study concluded that amelioration of radiation-induced fibrosis is mediated through suppression of senescence in type 2 pneumocytes [91]. Similar results have been revealed following inhibition of Bcl-2/xl. A study by Pan et al. has shown that inhibition of Bcl-2/xl by ABT-263 can kill senescent pneumocytes, which cause suppression of pulmonary fibrosis after lung irradiation [92]. In addition to fibrosis, senescence has been observed in other organs such as bone marrow and heart, which can trigger the release of some cytokines such as TGF-β, which may be involved in chronic oxidative stress [93]. It has been suggested that senescence after exposure to radiation can trigger activation of NADPH oxidase enzymes that are associated with increased superoxide and hydrogen peroxide generation [93]. Suppression of senescence can blunt upregulation of NOX enzymes, thus prevents continuous production of free radicals and subsequent consequences such as fibrosis [94]. Furthermore, reduction of senescence has been shown to be associated with the mitigation of radiation toxicity [95]. Role of senescence in cancer response to radiotherapy is complicated and unclear [96] (Fig. 2).

Fig. 2.

Radiation-induced senescence triggers the activity of pro-oxidant enzymes and fibrosis

Targeting of senescence during radiotherapy and its consequences on tumor response need further examination. However, evidences have shown that inhibition of PAI-1 can induce apoptosis in cancer cells [97]. Genetic knockdown or pharmacological inhibition of PAI-1 has been shown to induce apoptosis in a wide range of cancer cells such as HT-1080 fibrosarcoma, ovarian cancer cells, A549, HCT-116 human colon carcinoma, MDA-MB-231 human breast adenocarcinoma etc.[98, 99]. PAI-1 has a close role with angiogenesis and tumor growth. Thus, its targeting has been proposed to suppress angiogenesis [100]. PAI-1 inhibition can protect endothelial cells against apoptosis and aids the migration of these cells towards fibronectin [101, 102]. Therefore, it seems that targeting PAI-1 can protect some normal tissues such as the lung, while it is able to increase response of some cancers including lung, breast and colon to radiotherapy.

Targeting of inflammation

Inflammation after exposure to a high dose of radiation is involved in several complications caused by radiation. Inflammation is a normal response to massive cell death, which is mediated via some inflammatory mediators such as NF-κB, STATs, COX-2, iNOS etc. [103]. Dermatitis is one of the most common side effects of radiotherapy. Following the Chernobyl accident, some people died because of severe damages and reactions in the skin. Mucositis in the mouth and gastrointestinal system, necrosis in the brain, damage to vessels, pneumonitis and pericarditis are the most common consequences of inflammatory responses to ionizing radiation [104–107]. Inhibition of inflammatory mediators has been suggested to mitigate several complications after exposure to radiotherapy or an accidental radiation disaster [108]. Furthermore, as inflammation plays a key role in the progression of fibrosis, its inhibition can improve the management of fibrosis in different organs [109].

NF-κB

NF-κB is a central player of innate immune system. It regulates several signaling pathways involved in inflammation, proliferation and apoptosis [34]. The upregulation of NF-κB in highly radiosensitive organs such as bone marrow, testis or small intestine following activation of TLRs has been shown to be associated with protection and mitigation of mortality through suppression of apoptosis and preventing depletion of progenitor cells [57]. However, selective inhibition of NF-κB has been shown to protect bone marrow against toxic effects of ionizing radiation [110]. Furthermore, chronic upregulation of NF-κB plays a key role in chronic inflammation, which is associated with several side effects in normal tissues. Although the upregulation of NF-κB can reduce the incidence of apoptosis in early responding organs such as bone marrow, its suppression has been shown to be associated with the reduction of some side effects of ionizing radiation. An animal study suggested that suppression of NF-κB using the thiol-reactive triterpenoid RTA 408 can protect some radiosensitive organs including gastrointestinal, skin and hematopoietic system. Administration of this agent has shown significant increase in survival [111]. Suppression of NF-κB or upregulation of IκB can induce hematopoiesis and the activity of hematopoietic progenitor cells [110]. Protective effect of NF-κB suppression has also been observed for other organs such as the brain, kidney and gastrointestinal system following administration of different types of NF-κB inhibitors. Interestingly, inhibition of NF-κB showed a reduction of apoptosis in the brain [112]. It has been suggested that some radioprotectors and mitigators such as melatonin, curcumin, resveratrol, soy isoflavones and naringin are able to suppress the expression and nuclear translocation of NF-κB [34, 113, 114]. It seems that the suppression of NF-κB by these agents is a key mechanism for protection or mitigation of radiation injury [115–117].

NF-κB plays a key role in the resistance of a wide range of cancer cells to ionizing radiation. It can induce anti-apoptosis genes such as Bcl-2. NF-κB has a higher expression in several cancer types and its inhibition may enhance the death of cancer cells by radiation without adverse effects on normal tissues [34]. Furthermore, NF-κB increases angiogenesis and metastasis via regulation of vascular endothelial growth factor (VEGF), matrix metalloproteinase-3 (MMP-3), signal transducer and activator of transcription 3 (STAT3) etc. [34]. NF-κB upregulation has a link with a wide range of cancers such as hematological malignancies, lung carcinoma, gastrointestinal and breast tumors [118]. Some clinical studies have shown that the suppression of NF-κB is associated with an increase in the survival of patients with multiple myeloma [119, 120]. Targeting NF-κB has been shown to sensitize cancer cells to radiotherapy, thus its inhibition can increase the therapeutic efficiency of radiotherapy with both protection of normal tissues and sensitization of cancer cells [34].

COX-2

COX-2 generates prostaglandins (PGs) through the metabolism of arachidonic acids. PGE₂ is one of the most important products of COX-2 which mediates the pathogenesis of several inflammatory responses [121]. The expression of COX-2 is not high in all organs. However, its suppression has been shown to protect and mitigate radiation injury in some organs. In bystander effect, studies have shown that COX-2 plays a key role in DNA damage and cell death after exposure to ionizing radiation [122–125]. It has been suggested that upregulation of COX-2 is associated with mocusitis; however, it may not be a key player in the inhibition of this process [126]. Overexpression of COX-2 has also been observed in irradiated intestinal mucosa [127].

Inhibition of COX-2 using celecoxib or rofecoxib can alleviate the severity of arthritis and paw edema, and reduces the level of inflammatory cytokines such as TNF-α following exposure to radiation [128, 129]. COX-2 inhibition has also shown protection against radiation-induced skin injury [130]. Targeting COX-2 after irradiation has been shown to mitigate radiation injury in the bone marrow. Inhibition of PGE₂ synthesis using meloxicam after irradiation can mitigate mortality. Post-irradiation treatment with meloxicam could also improve hematopoietic system recovery. The mitigation of radiation-induced lethal effect was obtained when meloxicam was administered either 6 or 48 h after exposure to radiation [131]. COX-2 inhibition can also mitigate pulmonary injury after exposure to ionizing radiation [132]. It has been suggested that COX-2 inhibition is involved in the radioprotective effect of some agents such as curcumin [133]. By contrast, some evidences have shown that PGE2 has a role in protecting the intestines and hematopoietic stem cells [134, 135].

COX-2 inhibitors have been shown to sensitize cancer to radiation through suppression of proliferation, angiogenesis and metastasis. COX-2 is a stimulator of VEGF, thus it triggers angiogenesis and tumor growth [136]. COX-2 also induces the expression of anti-apoptosis genes such as Bcl-2, thereby increasing survival following therapy [137]. Due to these reasons, COX-2 inhibitors are known as radiosensitizers [138]. Targeting COX-2 has shown promising results for increasing tumor response to radiotherapy [139]. On the other hand, celecoxib as a selective COX-2 inhibitor can mitigate lung injury. It seems that COX-2 inhibition is interesting for protection and mitigation of radiation-induced lung injury. Other radiosensitive organs will require further examination in clinical studies.

NLRP3 inflammasome

NLRP3 inflammasome is a complex that reacts to stress conditions and pathogens through the release of IL-1 and IL-18. Regulation of this complex has a close relationship with mitochondria injury. Damage to the mitochondria may induce upregulation of NLRP3 inflammasome, thus amplifies inflammatory reactions [140]. Irradiation of macrophages lead to the development of NLRP3 inflammasome complex as well as an increase in pro-inflammatory IL-1 level [141]. This can promote apoptosis in radiosensitive bone marrow cells [142]. Activation of NLRP3 inflammasome has been shown to promote inflammation and fibrosis in some organs such as central nervous system (CNS), gastrointestinal system and lung [143]. In fact, NLRP3 inflammasome may accelerate inflammation and fibrosis following exposure to ionizing radiation [144]. Pyroptosis in bone marrow cells has shown as a key stimulator of NLRP3 inflammasome which acts as a key player in the bone marrow injury and mortality following whole-body irradiation [142]. Activation of NLRP3 inflammasome in immune cells also may play a key role in side effects of other tissues [141]. Inhibition of inflammatory pathways including NLRP3 inflammasome can mitigate radiation toxicity [145]. Melatonin, an anti-inflammatory agent, is able to mitigate radiation-induced mucositis through attenuation of NLRP3 inflammasome pathway [146, 147] (Fig. 3).

Fig. 3.

Inflammatory responses following exposure to ionizing radiation. Necrosis, necroptosis or autophagy can induce inflammatory responses following the release of DAMPs. NF-κB is a central regulator of inflammatory responses via triggering the release of cytokines and upregulation of COX-2 and iNOS. NF-κB also induces the development of inflammasome. Increased levels of inflammatory cytokines, iNOS and COX-2 amplify oxidative stress and DNA damage, which lead to continuous expression of NF-κB. The positive feedback between inflammatory cytokines, oxidative stress and transcription factors like NF-κB can cause chronic inflammation many years after exposure to radiation. Disruption of this crosstalk can mitigate radiation injury

Experimental studies have confirmed that NLRP3 inflammasome has a role in the pathogenesis of cancer. NLRP3 inflammasome is involved in cancer progression in a wide range of malignancies such as lung, skin, liver, gastrointestinal and prostate cancers [148]. Targeting NLRP3 inflammasome has been proposed for reducing tumor resistance [149, 150]. However, the effect of NLRP3 inflammasome targeting in combination with radiotherapy remains to be elucidated.

Absent in melanoma (AIM)2 inflammasome

AIM2 inflammasome is another type of inflammasome that has a role in cell death through pyroptosis. Pyroptosis is an inflammatory type of cell death that is mediated by inflammasomes [151]. After exposure to clastogenic agents and DNA damage, AIM2 recognizes double-strand breaks (DSBs), then stimulates the activation of caspase-1, the cleavage of gasdermin D (GSDMD) and release of inflammatory cytokines which is associated with membrane perforation and release of cell contents [152–154]. Although studies for protection against ionizing radiation via targeting AIM2 inflammasome is very limited, some results are interesting. For the first time, Hu et al. found that mice deficient in AIM2 are more resistant against mortal effects of whole-body exposure to ionizing radiation. Knockdown of AIM2 was shown to reduce pyroptosis in both bone marrow and intestine as well as preserved colony formation of stem/progenitor cells. Results of this study confirmed that AIM2 translocates into the nucleus after irradiation and mediates pyroptosis following activation of caspase-1 [155]. Inhibition of this pathway after irradiation also showed remarkable mitigation of radiation injury in the intestine. After whole-body irradiation, an increase in AIM2 and the cleavage of GSDMD was observed in the intestine, however, inhibition of AIM2 following administration of 5-Androstenediol mitigated intestinal injury and reduced mortality [156]. AIM2-induced pyroptosis is also involved in late effects of ionizing radiation including lung pneumonitis and fibrosis. Suppression of AIM2 can attenuate radiation-induced cell death in lung tissues, which is associated with amelioration of pneumonitis and fibrosis [157].

Heat shock proteins (HSPs)

HSPs are inflammatory mediator proteins that protect cells during stress conditions. It seems that oxidative stress and released cytokines after exposure to stimulus such as ionizing radiation trigger activation of HSPs [158]. HSPs include different subfamilies that may promote or suppress inflammation [159, 160]. HSP70 can prolong G1 phase of cell cycle, leading to the reduction of cell death after exposure to ionizing radiation [161]. In contrast to HSP70, HSP27 is an inflammatory mediator protein. HSP27 has a close relation with NF-κB, thus it can induce inflammation and suppress apoptosis [162]. Inhibition of HSP27 has been shown to reduce inflammation and oxidative stress following lung exposure to radiation [163]. Studies for the mitigation of radiation injury by inhibition of HSPs are very few.

Inhibition of HSP70 is an interesting strategy for tumor sensitization and activation of immune system against cancer [164]. HSP70 has high expression in a wide range of cancer cells, hence improving survival through stimulation of anti-apoptosis genes [165, 166]. Overexpression of HSP70 is associated with malignancy and metastasis in some cancers such as acute myeloid leukemia, hepatocellular carcinoma and cervical cancers [167]. Thus, its activation does not seem to be an appropriate strategy for normal tissue protection during radiotherapy. By contrast, inhibition of HSP27 can be a potential strategy for tumor radiosensitization. HSP27 has a role in the inhibition of apoptosis via inhibition of caspase 9. It can also suppress necrosis in cancer cells, leading to tumor resistance [168]. The expression of HSP27 can predict mortality of patients with lung carcinoma [169]. HSP27 inhibitors can cause both the protection of normal tissues and sensitization of tumor in combination with chemotherapy drugs or radiotherapy [170]. However, targeting HSPs for the mitigation of radiation injury requires further studies.

Hypoxia

Hypoxia is a low oxygen condition within tissues. Hypoxia is a critical issue for tumor response to therapy. However, evidence shows that it also plays a key role in normal tissue injury. Hypoxia stimulates angiogenesis through upregulation of hypoxia-inducible factor (HIF). HIF-1 is the main mediator of VEGF, which is responsible for the development of new vessels. Although angiogenesis causes serious resistance of tumors to radiotherapy, it is a marker of radiation-induced severe injury in normal tissues [171]. Hypoxia occurs when radiation kills endothelial cells, leading to the removal of microvascular [172]. This causes the reduction of vascular density, which leads to oxygen deprivation [173]. Hypoxia and nutrition deprivation following vascular depletion can give rise to necrosis of normal adjacent cells, which lead to inflammation and more amplification in normal cells [174]. For example, in the brain, hypoxia and vascular injury cause reduction of cognition for patients that undergo radiotherapy for brain tumors [173, 175]. It has been shown that hypoxia is a critical issue for late effects of ionizing radiation such as myelopathy, pneumonitis and fibrosis rather than early effects [171, 176, 177]. A radionuclide lung perfusion study showed that hypoxia increases with time after irradiation, which is associated with continuous increase in oxidative stress and the levels of VEGF and TGF-β [178].

HIF-1 plays a key role in hypoxia-induced oxidative injury, inflammation and fibrosis following lung irradiation. It can increase the expression of VEGF, TGF-β and inflammatory cytokines that activate redox reactions and finally facilitates fibrosis and pneumonitis [179]. In addition to the lung, HIF-1 may play a key role in the inflammatory reactions in other organs such as the intestine [180]. In contrast to HIF-1, upregulation of HIF-2 has been shown to protect normal tissues against radiation [181].

Hypoxia is known as a regulator of tumor resistance rather than normal tissue injury [182]. In response to hypoxia, HIF-1 stimulates VEGF and angiogenesis. Furthermore, HIF-1 can increase survival of cancer cells via induction of COX-2 [183]. Thus, targeting hypoxia does not interfere with tumor response to radiotherapy. The effects of hypoxia and HIF-1 on the resistance of a wide range of cancers such as lung, liver, brain, breast, prostate, cervix are well known. Thus, its targeting has been suggested to help overcome the resistance of a wide range of solid tumors and also amelioration of toxicity in adjacent normal tissues during radiotherapy [182].

Targeting fibrosis

Radiation-induced fibrosis can affect most irradiated tissues some months to years after exposure to heavy doses of ionizing radiation. Fibrosis is associated with deposition of collagen which leads to stiffness of tissues. In the muscles, fibrosis can cause stiffness, atrophy and shortening, which limit mobility [184]. This causes problems in the movement of joints and skin breakdown [185]. Fibrosis in the lung may appear the following radiotherapy for chest cancers, leading to pulmonary failure and death [186]. In the heart also, fibrosis increases the risk of heart attack [187]. Studies explaining the cellular and molecular mechanisms of radiation-induced fibrosis are ongoing. However, it is well known that the pivotal role of some cytokines such as TGF-β, IL-4 and IL-13 as well as some other mediators such as renin–angiotensin system and some microRNAs have shown important roles.

Interestingly, fibrosis which leads to tumor stiffness is an important cause of tumor resistance and progression [188]. TGF-β, IL-4 and IL-13 as pro-fibrotic cytokines are the most important suppressors of natural killer (NK) cells and cytotoxic T lymphocytes (CTLs), which cause immune escape of cancer cells [189]. Tumor fibrosis also reduces the penetration of anti-cancer drugs such as chemotherapy and immunotherapy into tumor microenvironment [188]. This effect can reduce the effectiveness of combination modalities such as chemoradiotherapy or immunoradiotherapy. Targeting fibrosis can increase the therapeutic efficiency of radiotherapy through normal tissue protection and also increasing tumor response to radiotherapy.

Pro-fibrotic cytokines

Fibrosis is a late effect of radiotherapy that may appear years after the end of treatment [190]. Fibrosis occurs following deposition of collagen and upregulation of extracellular matrix (ECM) components. Cell death through apoptosis and senescence, oxidative stress and chronic inflammation are key enhancers of fibrosis [191]. Fibrosis is a serious threat for some organs such as lung, skin, heart, intestine and also vessels [192, 193]. Fibrosis in the lung and heart poses a threat to the lives of patients that underwent radiotherapy for chest cancers and may cause death some years after radiotherapy. In the skin and intestine, fibrosis negatively affects the quality of life [194].

TGF-β

TGF-β is the central regulator of collagen deposition and fibrosis development following exposure to ionizing radiation. It is a key regulator of wound healing. However, massive apoptosis and senescence after exposure to high doses of ionizing radiation can cause abnormal upregulation of TGF-β for long times. TGF-β can increase the expression of pro-fibrosis pathways such as Smad2/3 and Rho/Rock pathways, which amplify the expression of ECM. TGF-β is also a potent stimulator of pro-oxidant enzymes such as NADPH oxidase, COX-2 and iNOS, which mediate the generation of ROS, NO and PGE₂; which are key players of fibrosis [191]. In response to ionizing radiation, TGF-β has also been shown to induce fibrosis through canonical WNT/β-catenin pathway and PPARγ [17, 195]. Clinical studies have shown that upregulation of TGF-β has a direct relationship with fibrosis in the lung, heart, skin, intestine, bladder, liver etc. [196, 197]. To date, several pharmaceutical agents, antioxidants and radioprotectors have been investigated for mitigating radiation-induced fibrosis through modulation of TGF-β. Cu/Zn superoxide dismutase (SOD) has been shown to reduce radiation-induced fibrosis in the skin through the modulation of TGF-β [198]. Stimulation of SOD has also shown anti-fibrosis effects in the lung [199]. Some agents such as melatonin, curcumin, selenium, MnTE-2-PyP5+, etc., are able to induce SOD after exposure to radiation, thus they may be appropriate candidates for mitigation of fibrosis after exposure to heavy doses of ionizing radiation [200–204]. Experimental studies have shown that some agents such as flaxseed, EUK-207, IPW-5371 and genistein can reduce the expression of TGF-β and mitigate radiation-induced fibrosis [205–207].

TGF-β is one of the most potent immune system suppressors in a wide range of malignancies via suppression of CTLs and NK cells [208]. Furthermore, the release of TGF-β will be increased following radiotherapy in both tumor and normal tissues. In this situation, increased level of TGF-β causes immune escape of cancer cells as well as normal tissue toxicity [209]. Hence, inhibition of TGF-β has been suggested to overcome cancer resistance and also normal tissue protection during radiotherapy [210].

IL-4

IL-4 plays a key role in the promotion of fibrosis. IL-4 can induce upregulation of TGF-β, which leads to stimulation of its downstream genes. Knockdown of IL-4 in mice has been shown to attenuate infiltration of macrophages in the lung [211]. It seems that IL-4 is able to upregulate the expression and activity of pro-oxidant enzymes, thus stimulates the production of free radicals and differentiation of myofibroblasts. Duox1 and Duox2 are the most important ROS generating enzymes that upregulate their expression following increased release of IL-4. Suppression of IL-4 and both Duox1 and Duox2 has been shown to be associated with the reduction of radiation-induced fibrosis in the lung. Some radioprotectors such as melatonin and selenium have also shown abilities to reduce infiltration of macrophages that is also associated with the reduction of IL-4 level and inhibition of its downstream signaling pathways.

IL-4 has a high expression in some cancers such as that of the lung, breast, glioma, bladder, pancreas and ovary [212]. In tumor, IL-4 promotes the development of T helper cells type 2 (Th2), while it suppresses proliferation of Th1. These effects lead to attenuation of anti-tumor immunity because of reduction of IFN-γ and IL-2, which are responsible for the proliferation of CTLs and NK cells [213]. In response to radiation, it has been suggested that IL-4 induces proliferation of cancer stem cells (CSCs) in prostate cancer cells [214]. Also, it promotes epithelial-mesenchymal transition in breast cancer cells after irradiation [215]. As suppression of IL-4 can protect lung tissues and inhibit lung and breast cancers, its targeting favours radiotherapy for these malignancies. For other tissues, targeting IL-4 will require further studies to examine its potentials for normal tissue sparing.

IL-13

Similar to IL-4, IL-13 can promote radiation-induced fibrosis. Although the complete mechanisms of the role of IL-13 in the development of radiation toxicity remain to be elucidated, it has been suggested that IL-13 through triggering of IL13Rα2 induces fibrosis [216]. Knockdown of IL-13 in mice has been shown to reduce the severity of lung fibrosis [217]. Interestingly, targeting IL-13 has been suggested for boosting tumor immunity as well as inhibition of IL-13 in some cancer cells including MCA304 sarcoma, 4T1 breast carcinoma and glioma cancer cells [218–220]. For mice bearing glioma, inhibition of IL-13 has been shown to increase survival [221]. The combination of radiation and IL-13Rα2-targeted cytotoxin has shown promising results for glioma cancer cells [222, 223]. Studies examining the effects of IL-13 on both tumor and normal tissues are very limited and need to be investigated for each organ and tumor.

Renin–angiotensin system

It is well known that renin–angiotensin system has a key role in the development of late effects of ionizing radiation [224]. Infusion of angiotensin II can augment radiation nephropathy [225]. Furthermore, it has been suggested that angiotensin antagonists can reduce the severity of radiation-induced nephropathy [226, 227]. Total body irradiation can increase the level of renin and the expression of angiotensin some weeks after irradiation, which can cause damages to some organs such as kidney, heart, brain, and lung [227–229]. The elevated level of renin–angiotensin can impair the function of kidney and heart, and also stimulates synthase of collagen and development of fibrosis [230, 231]. As the level of renin and angiotensin increases during some weeks to months after exposure to ionizing radiation, it is a potential candidate for mitigation and treatment of radiation-induced side effects. The most important side effects of renin–angiotensin system following exposure to ionizing radiation are renal malfunction and inflammation as well as fibrosis in some organs such as the lung, heart and kidney.

In the kidney, blockade of both angiotensin I and II may be critical in achieving maximum protection against radiation-induced kidney failure [232]. However, a study showed that treatment with an angiotensin II inhibitor can prevent renal failure following whole-body irradiation [233]. In a case report, it was shown that losartan as an angiotensin II inhibitor, can treat renal damage caused by radiation [234]. Comparisons between the different types of angiotensin-converting enzyme inhibitors (ACEI) suggest that captopril is a gold standard ACEI for mitigation of renal nephropathy [235]. Administration of captopril or losartan starting 10 days after whole-body irradiation showed delayed initiation of renal failure [236]. So far, few clinical studies have been conducted to show the mitigatory effect of ACEIs on renal failure after total body irradiation (TBI). A study showed a decline but not significant reduction in renal failure for patients who received hematopoietic stem cells after TBI [237]. However, another study showed a significant improvement in the glomerular filtration rate (GFR) [238]. It has been suggested that the overexpression of heme oxygenase 1 (HO-1) following upregulation of angiotensin II has a role in renal injury caused by ionizing radiation [239]. However, further studies will be required to explain the mechanisms involved in angiotensin II-induced renal function injury.

Inhibition of renin–angiotensin using some agents such as captopril, losartan, enalapril and fosinopril has been shown to mitigate radiation-induced pneumonitis and fibrosis [240, 241]. The combination of renin–angiotensin antagonist captopril with an antioxidant showed more reduction in pneumonitis following lung irradiation, which is an indication that renin–angiotensin can promote inflammation and fibrosis independent of redox system [242]. Delayed treatment with captopril starting from 2 weeks after lung irradiation has also been shown to reduce damages to pulmonary vascular [243]. The use of ACEIs has been suggested to prevent or mitigate radiation-induced pneumonitis in radiotherapy patients [244]. The use of ACEIs for lung cancer radiotherapy patients has shown lower incidence of lung pneumonitis [245]. Similar results were observed in a retrospective study for patients who used ACEIs during radiotherapy [246]. A clinical study also showed promising results for patients who underwent stereotactic body radiotherapy (SBRT) for lung cancer [247]. Lung pneumonitis and renal failure are two important side effects of total body irradiation (TBI) for patients with leukemia. Administration of ACEIs after TBI and hematopoietic stem cell transplantation showed a significant reduction in the incidence of pneumonitis. Captopril showed a reduction in the probability of pneumonitis by 15% [237].

Although the complete mechanisms of renin–angiotensin induced pneumonitis and fibrosis remain to be elucidated, it seems that triggering pro-fibrotic cytokines and mediators by renin–angiotensin has a key role. A study by Molteni et al. confirmed that inhibition of angiotensin II using captopril or enalapril is associated with potent inhibition of TGF-β, COX-2, alpha-actomyosin (α-SMA) thromboxane (TXA2) and PGI₂; which are key players in the progression of pulmonary fibrosis [248]. It has been suggested that renin–angiotensin inhibitors can increase the level of heptapeptide angiotensin-(1–7), which causes inhibition of inflammatory mediators such as COX-2 and MAPKs [249]. Furthermore, administration of captopril and other renin–angiotensin inhibitors have been shown to reduce the expression of PAI-1, an important regulator of senescence and fibrosis [250].

Administration of ACEI has also been shown to mitigate radiation toxicity in the bone marrow. Administration of captopril after whole-body irradiation can increase survival, while its administration before irradiation has been shown to reduce survival. Results indicated that administration of captopril only after exposure to radiation can cause bone marrow recovery [251]. Treatment with captopril even after 21 days has been shown to stimulate bone cells’ recovery [252]. It seems that an increase in angiotensin-(1–7) has a role in bone marrow recovery [253].

Angiotensin II has a key role in cancer immunosuppression. It can stimulate the expressions of TGF-β, COX-2, VEGF as well as others which promote tumor growth [254]. Inhibition of angiotensin II has been shown to suppress the growth of colorectal, renal and various types of lung cancer cells [255]. Due to the anti-cancer effects of angiotensin inhibitors on lung cancer as well as its protective effect on normal tissues, the combination of renin–angiotensin system inhibitors with radiotherapy may be applicable for lung cancer patients as shown by promising results from clinical studies [244, 256].

Epigenetic modulators

Epigenetic changes including modifications in the DNA methylation and histone acetylation play a key role in ionizing radiation-induced fibrosis [257]. ROS generation and DNA damage lead to several changes in the expression of miRNAs, DNA methylation and histone acetylation [258, 259]. In this section, we explain some epigenetic targets that are involved in the progression of fibrosis and suggested as potential targets for mitigation of radiation-induced fibrosis.

Bromodomain and extra terminal (BET)

BET proteins are involved in the reading of epigenetic histone modifications. BET proteins act as enhancer of the expression of target genes [260]. These proteins include four subfamilies that regulate the expression of some oncogenes and redox mediators. BET proteins are able to inhibit SOD expression, an important suppressor of fibrosis progression. Furthermore, BET proteins trigger myofibroblast differentiation following stimulation of TGF-β–NOX4 signaling pathway [261]. Silencing BET proteins has been proposed for preventing and also reversing fibrosis [262, 263]. So far, few studies have been conducted to explain the role of BET proteins in radiation-induced fibrosis. BET inhibitor JQ1 showed promising results for the reduction of inflammation and fibrosis following chest irradiation. Results indicated a reduction in pro-fibrosis genes and the differentiation of myofibroblasts [264]. Targeting BET can also regulate the expression of genes involved in fibroblast activation through activation of the diacylglycerol kinase alpha (DGKA). DGKA is an enhancer of alpha smooth muscle actin (α-SMA) and collagen 1A1 (COL1A1). Inhibition of BET proteins can cause reduction of DGKA gene expression, thus mitigates radiation-induced fibrosis [265]. Targeting BET proteins has shown anti-cancer effects for breast, colorectal, glioma, medulloblastoma, prostate and lung cancers [266, 267]. Clinical studies have also shown interesting results [268]. Thus, inhibition of BET may be promising for the amelioration of lung toxicity among patients with lung cancer.

MiR-21

It has been suggested that miR-21 has a close relation with TGF-β [269]. MiR-21 overexpression is associated with upregulation of TGF-β and fibrosis following exposure to ionizing radiation [270]. Upregulation of miR-21 after irradiation can suppress phosphatase and tensin homolog (PTEN) [271], leading to the induction of epithelial to mesenchymal transition (EMT), a key player of fibrosis [272]. MiR-21 overexpression has been shown to be associated with radiation-induced fibrosis [273]. MiR-21 as an inducer of fibroblast senescence causes the release of TGF-β from macrophages [274, 275]. As earlier mentioned, SOD is an important suppressor of radiation-induced fibrosis. One of the most common roles of miR-21 is inhibition of SOD2. TGF-β can induce the expression of miR-21 in fibroblasts, which cause the suppression of SOD and oxidative injury [276]. Downregulation of miR-21 has been suggested for reducing oxidative stress, inflammation and fibrosis following irradiation of the heart [277]. (Table 1).

Table 1.

Summary results of protection and mitigation of radiation-induced toxicity using inhibition of cellular and molecular targets

Route	Cells/tissues	Radiation dose	Targets	Findings	References
In vitro	Hella cells	2 or 5 Gy	BP53	Enoxacin enhances DNA repair capacity via facilitating recruitment of BP53 to damaged DNA sites	[36]
In vitro/ in vivo	U2OS and HEK293 cells/intestine	4 Gy/8.75 Gy	P53	Knockdown of βarrestin-1 causes MMD2 degradation and activation of p53, leading to an increase in DNA damage repair capacity	[37]
In vitro	Hs578T, DLD-1 and T98G cells	1–5 Gy	Ogg1	The expression of Ogg1 is involved in radioresistance	[38]
Mice	Gastrointestinal and hematopoietic system	9–25 Gy	P53	Suppression of p53 can help to cell cycle arrest and repopulation of progenitor cells in intestine epithelium	[41]
In vitro/ in vivo	Hematopoietic system	8 and 9 Gy	P53	Pifithrin-mu reduce p53 binding to Bcl-2 and Bcl-xL, leading to suppression of apoptosis and preventing hematopoietic system syndrome	[43]
In vitro/ in vivo	Hematopoietic system	8and 12 Gy	P53	Vanadate can blunt p53 interactions with mitochondria and apoptosis mediators, and also stimulates upregulation of anti-apoptosis Akt/PI3K pathway	[44]
Zebrafish	Hair cells in neuromasts	20 Gy	P38	Inhibition of p38 reduces apoptosis in auditory cells	[73]
Mice	Bone marrow	7.25 Gy	P38	Thioredoxin (TXN) as an inhibitor of p38 is able to reduce apoptosis and senescence in hematopoietic stem cells	[74]
Mice	Bone marrow	7.2 Gy	P38	Inhibition of p38 increases the effect of G-CSF for mitigation of lethal effects of ionizing radiation	[77]
Mice	Whol-body irradiation	5–30 Gy	NF-κB	Inhibition of NF-κB by ethyl pyruvate or RTA 408 increases survival of irradiated mice	[111]
Mice	Whole-body irradiation	6.5 Gy	NF-κB	Inhibition of NF-κB induces repopulation of progenitor stem cells in the bone marrow	[110]
Zebrafish embryos	Whole-body irradiation	20 Gy	NF-κB	A reduction of apoptosis in the brain reduced damage to kidney and intestine, and also an increase in survival observed following inhibition of NF-κB or IKK	[112]
Rats	Paw	7 Gy	COX-2	Celecoxib as a COX-2 inhibitor can reduce edema and the level of inflammatory cytokines such as TNF-α and IL-1. The level of PGE2 and oxidative stress also reduced	[128]
Mice	Chest	11.00–14.75 Gy	COX-2	Administration of celecoxib either 40 or 80 days after chest irradiation could reduce mortality	[132]
Rats	Intestine	7.5 Gy for 5 days	Inflammasome	Melatonin ameliorateed mucositis through suppression of NLRP3 inflammasome pathway	[147]
Rats	Oral	7.5 Gy for 5 days	Inflammasome	Melatonin reduces mucositis through inhibition of NF‐κB/NLRP3 inflammasome signaling	[146]
Mice	Bone marrow and intestine	14.2 Gy	AIM2	Knockdown of AIM2 causes reduced pyroptosis in both bone marrow and intestinal stem cells	[155]
Mice	Intestine	8, 9 and 10 Gy	AIM2	Targeting of AIM2 after whole-body irradiation can mitigate mortality through reduction of pyroptosis in the intestine	[156]
Mice	Lung	18 Gy	AIM2	Andrographolide could prevent translocation of AIM2 into nucleus in lung cells, leading to amelioration of lung pneumonitis and fibrosis	[157]
Mice	Lung	75 Gy	HSP27	Inhibition of HSP27 can reduce pneumonitis, leading to reduction of pro-inflammatory and pro-fibrosis cytokines, and attenuates pro-oxidant NOX4 enzyme activity and ROS	[163]
Rats	Skin	45 Gy	MiR-214	Inhibition of miR-214 reduces ROS generation by mitochondria which cause protection of mitochondria after irradiation	[286]
Mice	Lung	17 Gy	Bcl-2/xl	Inhibition of Bcl-2/xl using ABT-263 can kill senescent pneumocytes, leading to reduction of pulmonary fibrosis	[92]
Rats	Kidney	18.9–20.1 Gy	Renin–angiotensin system	After whole-body irradiation and bone marrow transplantation, inhibition of angiotensin II prevented renal failure	[233]
Human	Kidney	14 Gy	Renin–angiotensin system	Administration of captopril showed a significant reduction in renal failure following TBI and stem cells transplantation	[238]
Rats	Lung	10–15 Gy	Renin–angiotensin system	Inhibition of renin–angiotensin system by captopril or losartan mitigated radiation pneumonitis and increases survival	[240]
Rats	Lung	13 Gy	Renin–angiotensin system	Inhibition of renin–angiotensin system by captopril, losartan, enalapril or fosinopril mitigates radiation-induced pulmonary fibrosis	[241]
Rats	Lung	11 Gy	Renin–angiotensin system	Inhibition of renin–angiotensin system by captopril in combination with an antioxidant (EUK-207) is more efficient for mitigation of radiation-induced fibrosis	[242]
Human	Lung	23 or 39 Gy in 1 fraction, or 15 Gy in 3 fractions	Renin–angiotensin system	Using angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers could reduce signs of pneumonitis	[247]
Human	Lung	Mean lung dose was ≤ 20 Gy	Renin–angiotensin system	A reduction in pneumonitis signs was observed
Human	Total body irradiation	14 Gy	Renin–angiotensin system	Administration of captopril reduced pneumonitis. Renal failure showed a decline, while differences were not significant	[237]
Mice	Bone marrow	7.5 Gy	Renin–angiotensin system	Administration of captopril before whole body irradiation caused complete mortality while starting administration 1 h after irradiation led to 100% survival	[251]
Mice	Bone marrow	7.75–7.9 Gy	Renin–angiotensin system	Administration of captopril for 2 weeks after irradiation mitigated mortality. Captopril treatment 3 weeks after could reduce lethal effects of ionizing radiation	[252]
Rats	Lung	20 Gy	BET	Treatment with JQ1 1 day before to 9 days after chest irradiation led to remarkable reduction of collagen content and fibrosis. Furthermore, significant reduction in the expression of C-Myc oncogene, and pro-fibrosis genes including TGF-β, NF-κB p65, and Smad2/3 were observed	[264]
Rats	Heart	10 Gy	MiR-21	Suppression of miR-21 by molecular hydrogen-rich water caused reduction in inflammatory markers and possible fibrosis	[277]

MiR-21 is known as an important regulator of radioresistance of some malignancies including breast and lung [278]. This could ease the management of radiation-induced fibrosis in the lung without adverse effects on lung or breast cancer responses to radiotherapy [279].

The molecules with unclear selectivity

There are some other mediators that are mainly involved in cellular metabolism and potentiate radiation-induced oxidative stress. Targeting NADPH Oxidase enzymes including NOX1-5 and Duox1&2 have shown that can attenuate radiation injury in some normal cells/tissues. However, their inhibition has shown various consequences on the radiosensitivity of cancer cells [280, 281]. PPAR also is another target that has shown different effects. Some studies suggested that PPAR agonists can protect normal tissues [282]. However, this may increase cancer cells radioresistance [283]. Targeting of these molecules and some other targets such as mitochondria, iNOS, and mTOR need to more accuracy. Suppression of these mediators may reduce ROS and NO levels in tumor, leading to more survival following exposure to ionizing radiation [204, 284, 285] (Fig. 4).

Fig. 4.

Mechanisms of radiation-induced redox metabolism and its role in the progression of radiation-induced normal tissue injury

Regenerative medicine in the mitigation of ARS

Stem cells responses to ionizing radiation

Stem cells are critical targets for ionizing radiation. The primary reason for hematopoietic and gastrointestinal system is stem cell death, which leads to depletion of progenitor and mature cells during some days after exposure to radiation. Bone marrow is containing two types of multipotent stem cells, including mesenchymal and hematopoietic stem cells [59]. Mesenchymal stem cells are more radioresistant compared to hematopoietic stem cells. Furthermore, mesenchymal stem cells are responsible for the production of fatty cells and osteoblasts that are less critical following exposure to a radiation accident. By contrast, hematopoietic stem cells are responsible for maintain of immune system, red cells and platelets. Hematopoietic stem cells divide into two type progenitor cells, including myeloid and lymphoid cells. Hematopoietic stem cells have very low mitotic activity, while, progenitor cells have higher mitotic index and are more radiosensitive. Lymphoid progenitor cells and also its derivative cells containing lymphocytes have high radiosensitivity. High radiosensitivity of progenitor and mature lymphoid cells leads to fast depletion of lymphocytes in peripheral circulation which may continue for a long time after exposure to a high dose of radiation. Myeloid-derived cells such as neutrophils, platelets, monocytes, basophils and erythrocytes are radioresistant and no immediate reduction is observable after exposure to radiation. However, high radiosensitivity of myeloid progenitor cells lead to remarkable reduction of these cells during some days to weeks. These changes cause severe suppression of immune system.

Stem cells in intestine, especially jejunum have high mitotic activity. High self-renewal activity of stem cells in intestine maintains sufficient number of functional cells such as absorptive, epithelial and goblet cells. Functional cells are resistant to ionizing radiation. However, they have low life and then are shed into the lumen during some days. Continuous division of intestine stem cells provide sufficient surface for nutrient and water absorption by crypts and villi. High mitotic activity of intestine stem cells makes them sensitive to ionizing radiation. Damage to intestinal stem cells leads to depletion of goblet cells, shortening of villi and crypt thinning. Furthermore, apoptosis and necrosis of endothelial cells in vessels lead to bleeding and penetration of microorganisms into circulation. The existence of bacteria in circulation and also suppression of immune system can cause severe infection. Reduction of platelets also increase bleeding and more reduction of peripheral cells.

As mentioned earlier, redox interactions and continuous production of ROS and NO play key role in radiation toxicity. In the hematopoietic system and intestine ROS and NO can suppress DNA damage repair and cell cycle progression. Targeting of ROS generating sources such as NOX4, and also mitochondria has shown that reduces damage to hematopoietic stem and progenitor cells and improves hematopoietic function after irradiation. Scavenging of free radicals also can help to repair stem cells and mitigation of radiation injury in intestine [287]. WNT/beta-catenin plays a key role in the proliferation of stem cells and resistance to ionizing radiation [288]. Stimulation of this pathway can increase survival through the induction of repair pathway and suppression of apoptosis [287, 289]. Some other targets such as TLRs, p53 and angiotensin II are promising for stem cells protection, however, there need to studies to explain the role of these targets for each type of stem cells in bone marrow and intestine.

Stem cells therapy for mitigation of ARS

Bone marrow transplantation has been a known strategy for the regeneration of bone marrow function after bone marrow injury such as seen following ARS or total body irradiation for leukemia. Results from Chernobyl accident confirmed successful mitigation of ARS following bone marrow transplantation [290]. It was assumed that hematopoietic stem and progenitor cells are responsible for the regeneration of bone marrow function. However, nowadays it is well known that other stem cells such as mesenchymal, adipose or embryonic stem cells can regenerate radiation-induced stem cell depletion in the bone marrow and gastrointestinal system [291]. To date, some types of stem cells such as mesenchymal and embryonic stem cells have studied in animal studies to mitigate ARS following exposure to lethal doses of ionizing radiation [292–295]. MSCs have priority for transplantation because their immunoregulatory effects. MSCs are able to attenuate response of T lymphocytes, thus reduces transplant rejection probability [296]. Furthermore, transplantation of endothelial cells has shown that can mitigate ARS, mediated through the regeneration of hematopoietic stem cells, inhibition of apoptosis and also repair of injured vessels [297, 298].

Administration of MSCs to irradiated mice can reduce apoptosis and trigger stemness in both HSCs and stromal stem cells. MSCs are able to upregulate Notch2 signaling, an important regulator of hematopoiesis, thus triggers proliferation of both MSCs and HSCs after exposure to ionizing radiation [299]. MSCs also attenuate inflammation and endogenous free radicals, thus reduce vascular injury [257]. Using MSCs with high expression of high mobility group box 1 (HMGB1) has shown is more effective for mitigation of radiation-induced vascular injury. HMGB1-modified MSCs have higher potential for differentiation toward endothelial cells, thus can repair vessels more effectively [300].

Stem cells therapy in combination with ROS targeting for mitigation of ARS

As some stromal cells such as fibroblasts play a key role in redox reactions after ionizing radiation, inhibition of these targets may help to preserve remaining stem cells and also the success of stem cells transplantation [301]. Furthermore, targeting free radicals by antioxidants or ROS scavenging enzymes may be an interesting idea for better mitigation of ARS following stem cells therapy. A study reported the successful mitigation of ARS using genetic modified MSCs to release extracellular SOD [302]. Similar results observed for modified umbilical cord mesenchymal stromal cells [303]. Activation of ERK/NRF2 pathway is another suggested mechanism that has shown mitigate damage to hematopoietic stem cells [304]. NRF2 triggers the activation of antioxidant defense enzymes such as SOD, thus reduces apoptosis following exposure to ionizing radiation [304]. As SOD has shown that neutralize free radicals produced by stromal cells, activation of this pathway may help to the survival of remaining stem cells after exposure to radiation, or even attenuates damage to transplanted stem cells [305, 306].

Stem cell therapy for mitigation of delayed effect of acute radiation exposure (DEARE)

Although cell therapy can mitigate radiation toxicity in bone marrow and gastrointestinal system, damage to other organs such as kidney and lung need to mitigated through inhibition of other potential targets. Stem cell therapy can reverse the depletion of stem cells in irradiated organs and also attenuate some other side effects. It is reported that MSCs have some properties that help to management of radiation-induced inflammation and fibrosis in late responding tissues such as lung [307]. MSCs can help to restore of radiosensitive cells in the lung, including endothelial cells in vessels and epithelial cells in airways [308]. Furthermore, MSCs have the ability to restore antioxidant defense, thus attenuate oxidative stress [309]. MSCs can release SOD, thus can suppress chronic inflammation, oxidative stress and development of fibrosis in the lung [310, 311]. Clinical usage of stem cells for protection and mitigation of radiation-induced lung fibrosis is in the first steps (NCT02277145).

By contrast to mentioned studies, there is some evidence that stem cell therapy may cause increase progression of lung injury [312]. Furthermore, there are some experimental studies that indicated stem cell transplantation cannot mitigate kidney and lung injury following whole-body exposure to radiation [237, 313]. An experimental study showed that stem cell transplantation following whole-body irradiation with 10 Gy mitigates ARS in hematopoietic and gastrointestinal system. However, a remarkable reduction in survival observed during 15–20 weeks. Results showed a significant increase in BUN level, indicating nephropathy. Treatment with captopril or other renin–angiotensin inhibitors showed a significant reduction in the BUN level and increase of survival [235]. Another study also indicated that bone marrow transplantation after whole-body irradiation with 11 Gy lead to death during 2–4 months because of pneumonitis and kidney failure. However, when rats received renin–angiotensin inhibitors including captopril, enalapril or fosinopril, a significant increase in survival observed, which was associated with amelioration of pneumonitis and nephropathy [314]. A clinical study also confirmed that captopril administration after total body irradiation and bone marrow transplantation increase survival of patients [237].

Importance of time for the onset of radiation mitigation treatment against ARS and DEARE

Timing for initiation of treatment for mitigation of radiation lethality is a vital issue. It is predictable that kinetic of cells and also final consequence of ionizing radiation in each organ play key role in the selection of appropriated mitigators and also timing for supplement. ARS in the hematopoietic and gastrointestinal system is mainly resulting from apoptosis of stem and progenitor cells [315]. Early apoptosis occurs during some hours after exposure to ionizing radiation [316]. Thus, mitigation of ARS in hematopoietic and gastrointestinal system need to suppression of apoptosis at early hours after exposure to radiation. Targeting of p53 and TLRs has confirmed this issue. Inhibition of p53 or treatment with TLRs agonists can mitigate radiation toxicity effectively when treatment initiated during first hours after irradiation [19]. Early apoptosis is p53 dependent and its targeting need to treatment during first minutes to hours [317]. Second wave of radiation-induced toxicity in bone marrow and intestine may be trigger by activation of pro-oxidants and production of free radicals. These free radicals are not produced by ionizing radiation directly, but apoptosis and release of damaged cells contents can trigger ROS production by macrophages, lymphocytes and also mitochondria in some non-immune cells [318]. Neutralization of free radical using ROS/NO scavengers and also mitochondria targeting can suppress further apoptosis and depletion of progenitor cells [319]. Initiation of second wave of ROS production may take some hours to days. Thus, treatment with antioxidants immediately after exposure to radiation may do not cause remarkable improvement in survival and mitigation of ARS [320]. Renin–angiotensin is another known mediator of radiation toxicity in bone marrow. As showed in Fig. 5, it can stimulate upregulation of TGF-β, an important stimulator of apoptosis and redox activation. Targeting of renin–angiotensin system immediately after exposure to radiation to some weeks later can mitigate ARS, probably via inhibition of TGF-β induced apoptosis and chronic oxidative stress.

Fig. 5.

Suitable timelines for the mitigation of radiation injury in different organs. Each target may need a specific time in each organ. Information for some targets such as COX-2 require further studies. Furthermore, each antioxidant or anti-inflammatory agent may lead to different results, maybe because of their effects on other mechanisms. This timing is based on information adopted from animal studies

The time window for mitigation of DEARE is differ compared to ARS. In the kidney, stem cells have low kinetic and nephropathy can occur during a long time after exposure [321]. Pneumonitis and fibrosis also are late effects of ionizing radiation that may cause death during months to years after exposure to a high dose of ionizing radiation [322]. These side effects are resulting from chronic upregulation of inflammatory and pro-fibrosis cytokines and transcription factors [323]. Oxidative stress following cell death and activation of pro-oxidant enzymes plays a key role in the upregulation of inflammatory and fibrosis mediators. On the other hand, inflammation and fibrosis processes are associated with several changes including ROS and NO production. This process indicates that using ROS/NO scavengers and also some drugs that are able to inhibit inflammation and fibrosis can be used to suppress late effects of ionizing radiation in late responding organs [318]. Mitigation of radiation-induced kidney injury with selenium or angiotensin inhibitors can mitigate nephropathy. Shortening of supplement time showed reduced mitigation of nephropathy [235, 324]. For lung pneumonitis and fibrosis, treatment with antioxidants is necessary during the first 4 weeks. Treatment with flaxseed has shown that treatment during 2–4 weeks is more important compared to previous or later times [325]. Treatment with renin–angiotensin inhibitors or antioxidants including genistein and EUK-207 for longer times can mitigate lung injury. Furthermore, starting treatment as soon as possible may be more useful [326]. Delayed treatment for 4 weeks may abrogate the mitigation of lung injury [327]. Although delayed starting treatment with antioxidants can reduce radiation injury in the lung, it seems that longer time treatment is favor for mitigation of pneumonitis and fibrosis. However, this effect is highly depended on antioxidant or anti-inflammation agent. Another target for mitigation of radiation-induced lung injury is COX-2. A study showed an increased survival when celecoxib administration started at 80 days after chest irradiation [132]. The time effect of treatment with mitigators for lung pneumonitis and injury need further elucidation (Fig. 5).

Experimental models for ARS and DEARE

An important problem for confirmation and approve of a radiation mitigator is extrapolation of animal results to human. This is because it is not possible to test radiation mitigators for human. Thus, it is necessary to use standard animal models to compare results of different mitigator agents. Furthermore, it has been suggested that endpoints in animal models should be related to human, and pharmacodynamics of mitigators should be understood. For evaluating each endpoint, it is necessary to be noted that some genetic differences can affect radiation response in each strain [328].

ARS in hematopoietic and gastrointestinal systems are the most common studies for exploring new radiation mitigators. Mice, canine and nonhuman primate are three types of strains that have been used for investigating hematopoietic system study. The most common mice strains include C57BL/6, BALB/c, C3H/HeN and B6D2F1/J. Radiosensitivity of these strains is varied. Among these strains BALB/c is more radiosensitive. LD50/30 for BALB/c mice is lower than 7 Gy. This may relate to reduced activity of DNA PKcs, a critical DNA repair enzyme in BALB/c strains [328]. NMRI mice are another strain that have studies for several bone marrow experiments with a LD50/30 equal 7.2 Gy [329]. Among larger animals, rhesus macaque is the most common type of nonhuman primate for hematopoietic system model. For gastrointestinal system, C57BL/6, BALB/c were the most common types of strains for investigation of radiation mitigators. However, some other strains such as rats, dogs or non-human primates may be used for this aim [330].

Skin is another important tissue that reacts to ionizing radiation during the early days to several months after irradiation, depending on radiation dose. Rodents are the most common strains for investigating radiation dermatitis. However, skin responses in rodents vary and can be observed at different doses. Furthermore, investigation of dermatitis in some mice may be difficult because of their hairy and dark skins [328]. For skin responses to ionizing radiation, it has been suggested to use pigs instead of mice or rat’s models. This is because of more similar physiological responses and structure of skin in pigs with human [328]. Among large animals, non-human primates and dogs have the most similar immunological responses to human [331].

Lung and kidney are the most important late responding organs, which show different radiosensitivities among various strains. For kidney, rats are in priority among small animal models. Indeed, most researches for nephropathy models can be achieve using rat’s models, while mice show less response for renal following exposure to ionizing radiation [328]. Also, mice strains show different responses to ionizing radiation and recovery, thus it is not easy to compare results of different types of mice to radiation or radiomitigators [332, 333]. WAG/Rij strain rats are one of the most known strains for investigation of kidney diseases including radiation-induced nephropathy [334]. For lung responses, including pneumonitis and fibrosis, non-human primates and dogs have the most similar lung physiology for both pneumonitis and fibrosis. However, mice may show different responses for each of these endpoints [328]. It has been suggested that scientists use two strains of mice for evaluating mitigation of pneumonitis and fibrosis. C57BL/6 mice show extensive fibrosis but very low pneumonitis markers following lung irradiation. On the other hand, C3HeB/FeJ mice show more pneumonitis with no extended fibrosis [328]. Rats may be better candidate compared to mice for lung studies. Sprague–Dawley or WAG/RijCmcr rats show both acute pneumonitis and fibrosis following lung exposure to radiation [205, 241]. Furthermore, the heart, which is a late responding tissue, shows remarkable response following chest irradiation [335]. In this situation, both lung and heart tissues can be investigated for detecting mitigatory effects [336].

Conclusion

In conclusion, ionizing radiation causes several changes in the expressions of pro-inflammatory and pro-fibrotic genes, and also changes the normal metabolism of oxygen. These are as a result of massive DNA damage and cell death, especially through apoptosis, necrosis, necroptosis and senescence. Boosting DNA repair mechanisms and suppression of death mediators such as Bax can help reduce cell death caused by ionizing radiation. Furthermore, the induction of anti-apoptotic pathways has shown promising results. TLRs agonists are interesting for suppression of apoptosis in highly radiosensitive organs such as the bone marrow and intestine. It seems that TLRs can act as protector through modulation of early apoptosis genes. Similar results have also been observed for p53 inhibition. P53, an important regulator of DNA damage repair and apoptosis plays a key role in protection or mitigation of radiation toxicity in hematopoietic system. It seems that p53 has pivotal role in early apoptosis in bone marrow stem cells. Thus, inhibition of p53 immediately or during some early hours after exposure to radiation can increase resistance to ionizing radiation. However, its targeting during some days after exposure to radiation cannot act as a strategy for mitigation of radiation mortality. The roles of these targets in protection or mitigation of radiation injury in late responding tissues remain to be elucidated. However, in these organs such as seen in the lung, senescence and necrosis may be more important compared to apoptosis.

Inflammation and redox mediatory responses are critical targets for mitigation of radiation injury. This is important for both early responding tissues such as bone marrow as well as for late responding tissues such as the lung, kidney, heart, brain and spinal cord. Continuous ROS generation by the mitochondria and pro-oxidant enzymes such as NADPH oxidase promotes apoptosis and senescence in the bone marrow and intestinal progenitor cells. Inhibition of these ROS sources or neutralization of free radicals has shown significant mitigation of radiation mortality. In contrast to TLRs and p53, inhibition of oxidative stress through direct neutralization of free radicals by antioxidants or targeting of mitochondria and pro-oxidant enzymes can mitigate radiation injury even when treatment commences some days after exposure to radiation. Targeting of renin–angiotensin system after irradiation has been shown to mitigate radiation-induced hematopoietic and gastrointestinal system, even when treatment started some weeks after irradiation. Interestingly, suppression of angiotensin before irradiation may not protect these organs. Thus, the cellular and molecular mechanisms of this issue need to be studied.

For late responding organs such as the lung, heart, kidney, brain and gastrointestinal system, chronic inflammation and fibrosis are main concerns. Pro-inflammatory and pro-fibrotic cytokines including IL-1, IL-4, IL-13, TGF-β and TNF-α are important inducers. However, there are some other inflammatory and fibrosis mediators that can affect the release of these cytokines, or may be induced by them. Renin–angiotensin system, mTOR and senescence, hypoxia, epigenetic modulators such as BET and miR-21 are the common enhancers of radiation-induced fibrosis through TGF-β pathway. On the other hand, iNOS, NOX1&2&4, Duox1-2 and COX-2 are important downstream factors of pro-fibrosis cytokines. Targeting these factors can be proposed for the mitigation of radiation injury in these organs. However, their expressions are tissue specific, thus the need for further knowledge about the radiobiological response of each organ is critical for effective mitigation of radiation-induced normal tissue injury.

The timing of treatment with radiation modifiers is a very critical issue. Targeting of early apoptosis can be very effective for protection of radiosensitive organs. However, for an accidental radiological or nuclear disaster it is very difficult to mitigate hematopoietic and gastrointestinal system through this pathway. Thus, some targets such as TLRs and p53 may not be useful for mitigation of radiation injury in real situations. Targeting TLRs is effective before exposure to radiation or some hours after. Thus, TLRs are promising targets for radiation protection, however, mitigation of radiation injury using TLRs agonist acts in a limited time window. The role of TLRs in late responding radiosensitive organs such as the lung is complicated and some studies have shown different results. Although activation of TLRs can suppress apoptosis and ARS for early responding tissues, it is important to note that its role as an inflammatory mediator may cause the severity of late effects of ionizing radiation. In fact, suppression of TLRs may be more promising for late responding organs. Thus, TLRs agonists may be promising radioprotectors in clinical studies, however, their use as radiation mitigators needs further studies. Potent antioxidants and anti-inflammatory agents are interesting for both protection and mitigation via treatment before or after exposure to radiation. As redox interactions start to produce free radicals during some days after exposure to radiation, mitigation of radiation injury using ROS/NO scavengers or redox inhibitors can be done more effectively. In a real situation, treatment of injured people in an accident can be done through the administration of antioxidants starting from some days after the accident. In contrast to TLRs agonists and p53 inhibitors, the time for mitigation of radiation mortality is not very critical. Exposed persons to lethal doses of ionizing radiation may survive if treatments commence even after some days. A more extended time window has been observed for renin–angiotensin inhibitors. Inhibition of renin–angiotensin system can mitigate radiation injury in both early and late responding organs when treatment commence even some weeks after exposure to radiation.

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Conflict of interest

The authors declare no conflict of interest, financial or otherwise.