Abstract
Radiation-induced lung fibrosis, the most serious effect of lung cancer radiotherapy on normal tissue, remains a major technical obstacle to the broader application of radiotherapy to patients with lung cancer. This study describes the use of an image-guided irradiation system in mice mimicking stereotactic body radiotherapy (SBRT) to examine the molecular features of chronic fibrotic response after radiation injury. MicroRNA (miR) array analysis of injured pulmonary tissue identified a set of miRs whose expression was significantly increased in damaged lung tissue. In particular, miR-21 expression was increased at the radiation injury site, concurrent with collagen deposition. Although the inhibition of miR-21 by its specific inhibitor anti-miR-21 only marginally affected endothelial-mesenchymal transition (EndMT) in lung endothelial cells, this inhibition significantly reduced collagen synthesis in lung fibroblasts. Furthermore, ectopic expression of miR-21 was sufficient to promote a fibrotic response in lung fibroblasts, enhancing Smad2 phosphorylation concurrent with Smad7 downregulation. These findings indicate that the induction of miR-21 expression is responsible for fibrotic responses observed in mesenchymal cells at the injury site through the potentiation of TGF-β signaling. Local targeting of miR-21 at the injured area could have potential therapeutic utility in mitigating radiation-induced lung fibrosis.
Introduction
Radiation pneumonitis is one of the most frequent post-treatment complications of stereotactic body radiotherapy (SBRT), with symptoms ranging from mild to critical. In particular, radiation-induced lung fibrosis (RILF), which is characterized by the recruitment of fibroblasts, myofibroblasts, and leukocytes, resulting in the accumulation of extracellular matrix proteins, such as collagens, is a severe complication that may be life-threatening due to the impairment of normal breathing [1–3]. At present, steroid anti-inflammatory drugs are the only medical option for patients with a high risk of RILF onset prior to augmentation of the pathogenic response. However, no early diagnostic markers of RILF have yet been identified. Thus, understanding the molecular mechanism underlying the onset of RILF and identifying possible early markers for this condition may help in the development of alternative treatment strategies [4–6].
The onset of RILF is a complicated process that involves various cell types [1]. Because a marked increase in fibroblast accumulation, followed by collagen production, is the most common event in RILF, myofibroblasts and fibroblasts derived from various sources play key roles in pathophysiological fibrotic responses. Thus, novel strategies to control fibroblast accumulation or collagen production may be therapeutic in patients with RILF. Endothelial cells (ECs) injured by ionizing radiation (IR) or bleomycin have been found to acquire the cellular properties of fibroblasts in a process termed endothelial-to-mesenchymal transition (EndMT) [7–9]. EndMT is characterized by the expression of mesenchymal markers, including alpha-smooth muscle actin (α-SMA), vimentin, and fibroblast-specific protein-1 (FSP-1), and the increased production of collagens, particularly types I and III, with the latter responsible for the fibrotic responses of the ECs.
MicroRNAs (miRs) are small noncoding RNAs that bind to specific mRNA sequences and suppress target protein(s) expression by inhibiting translation or degrading mRNAs [10]. The expression of miRs has been shown to be upregulated or downregulated under various pathophysiological conditions [10]. The levels of expression of certain miRs, which can be readily determined in bodily fluids such as blood, serum, urine and saliva, have been extensively studied because of their possible applications as biomarkers for the early detection of several specific diseases [11–13]. Moreover, because the aberrant expression of certain miRs is closely associated with target protein expression, these miRs are responsible for the onset of pathophysiological responses in a disease condition. For example, miR-21, whose expression is upregulated in chronic inflammatory conditions or by transforming growth factor β (TGF-β), has been shown to potentiate TGF-β responses by downregulating the level of the inhibitory Smad, Smad7 [14]. In particular, miR-21 levels are significantly increased in the lungs of bleomycin- and TGF-β-treated mice and are involved in the pro-fibrogenic responses of TGF-β through the suppression of Smad7 [15]. These findings suggested that miR-21 may be a potential molecular target for modulating pulmonary fibrosis [15].
This study used an image-guided irradiation system in mice to mimic the radiation lung damage caused by SBRT and examined the molecular events occurring in the damaged lungs. Analysis of miR arrays showed that miR-21 was induced in damaged areas of the lungs and that miR-21 expression, along with the suppression of Smad7, contributed to collagen production by fibroblast-like cells after radiation damage. These findings suggest that a strategy to inhibit miR-21 induction after SBRT would be therapeutically effective in preventing the onset of RILF and RILF-associated pathological symptoms.
Materials and Methods
Reagents and cell culture
Primary antibodies against, ICAM-1 (sc-8439), p21 (sc-397), col3A1 (sc-28888), β-actin (sc-47778) and α-tubulin (sc-8035) were obtained from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Primary antibodies against alpha-smooth muscle actin (a-SMA) (#a5228) were purchased from Sigma (St Louis, MO, USA). Human pulmonary endothelial cells were maintained in endothelial cell growth medium MV2 (c-22022, promocell, Heidelberg, Germany) with 0.1% gentamicin (Sigma) at 37°C in a humidified 5% CO2 incubator.
Animal models and irradiation
All studies with mice were approved by the Yonsei University Medical School Animal Care and Use committee. As described previously [16], C57BL/6 male mice (8 weeks) were used for radiation-induced lung fibrosis research. To mimic SBRT conditions, 3-mm collimator to administrate a 90Gy of dose of radiation to the left lung was used for introducing the radiation damage. Right lung at each mouse was used for the control. Radiation was delivered with an X-RAD 320 (Precision, North Branford, CT, USA), equipped with a collimator system composed of 5-cm-thick copper to produce focal radiation beams. For positioning the radiated area, the image-guided devise with a motorized, 2D moving stage, a fluorescent screen (Kodak Min-R 2000; Carestream Health Inc., Rochester, NY, USA), and a charge-coupled device (CCD) camera (650D; Canon Inc., Tokyo, Japan) controlled by a mobile computer was used. Prior to irradiation, the mice were anesthetized with an intraperitoneally administered mixture of 30 mg/kg of zoletil and 10 mg/kg of rompun. The four legs of the mice were additionally fixed with adhesive tape. At 1, 2, 3 and 4 weeks after radiation, the mice were sacrificed. Four mice were allocated per group, and the experiment was repeated twice. The condition of animals after irradiation was monitored daily basis. The animals after irradiation lived normally until they were scarified at 3 or 4 weeks. The typical symptoms of high radiation exposure were observed such as hair loss and dermonecrosis at 2–3 weeks after irradiation. For lung harvesting, the mice were anesthetized with an intraperitoneally administered mixture of 30 mg/kg of Zoletil (tiletamine 25mg/kg with zolazepam 25mg/kg) and 10 mg/kg of Rompun (xylazine 10mg/kg), which produces general anesthesia in animal for 2–3 hours.
MicroRNA microarray and analysis
Total RNA of each sample was isolated by using the Trizol reagent (Life technologies, Inc., Carlsbad, CA) according to the manufacturer’s instructions. For control and test RNAs, the synthesis of target miR probes and hybridization were performed using Agilent’s miR Labeling Reagent and Hybridization kit (Agilent Technologies, Palo Alto, CA) according to the manufacturer’s instructions. All data normalization and selection of fold-changed probes were performed using GeneSpringGX 7.3 (Agilent Technologies). We performed data transformation (set measurements less than 0.01 to 0.01) and per chip (normalize to 75th percentile) normalization.
TaqMan Real-time PCR microRNA assay
Total RNA was extracted with Trizol reagent (Invitrogen) and miRs were detected via a TaqMan Real-time PCR microRNA assay (Applied Biosystems, Carlsbad, CA). In order to quantify the different expressions of specific miR, we analyzed the expression of miRs (miR-21; 000397, U6; 001937; Ambion, Austin, Tx) in the total RNA extracted from various tissue samples and cells via real-time PCR using a TaqMan microRNA Assay kit (Applied Biosystems, Carlsbad, CA).
RNA isolation and quantitative Real-Time PCR Analysis
Total RNA of each sample was isolated by using the Trizol reagent (Life technologies, Inc., Carlsbad, CA) according to the manufacturer’s instructions. Gene-specific primers are listed as follows: mouse col1A2 (forward: 5’-TGGTCTTACTGGGAACTTTGCTGC-3’, reverse: 5’-ACCCTGTGGTCCAACGACTCCTCTC-3’), housekeeping gene mouse GAPDH (forward: 5’-TATGGAAAGCTGTGGCCTGG-3’, reverse: 5’-CAGATGCCTGCTTCACCA CCTTC-3’), human ICAM-1 (forward: 5’-CGTGGGGAGAAGGAGCTGAA-3’, reverse: 5’-CAGTGCGGCACGAGAAATTG-3’), human aSMA (forward: 5'-CATCACCAACTGGGA CGACATGGAA-3', reverse: 5'-GCATAGCCCTCATAGATGGGGACATTG-3'), human fibronectin (FN) (forward: 5'-GTGTTGGGAATGGTCGTGGGGAATG-3', reverse: 5'-CCA ATGCCACGGCCATAGCAGTAGC-3'), human col1A2 (forward: 5'-GGTGGTGGTTATG ACTTTGG-3', reverse: 5'-TCTGGGTGGCTGAGTCTCAA-3'), human col3A1 (forward: 5'-GCTCTGCTTCATCCCACTATTA-3', reverse: 5'-AACATTCTCCAAATG GAATT-3') and housekeeping gene human b-actin (forward: 5’-GTCCTCTCCCAAGTCCACAC-3’, reverse: 5’-GGGAGACCAAAAGCCTTCAT-3’). All amplifications were conducted in a pre-mixture (20 ml) containing 500 nmol/l of gene-specific primers, and 6 ml of template, under the following conditions: denaturation at 95°C for 1 min, followed by 40 cycles of 95°C for 15 sec, 58°C for 15 sec, and 72°C for 15 sec, with a final extension at 72°C for 5 min. For PCR validation, amplified products were separated on 2% agarose gels and visualized by ethidium bromide staining. The reactions were carried out in Roche LC480.
In situ hybridization
miRCURY LNA™ microRNA ISH Optimization Kit (FFPE) was purchased from Exiqon (Vedbaek, Denmark). In situ hybridization was performed with 3μM-thick mouse lung tissues and all procedure was proceeded in RNase-free environment. ISH probe for miR-21 and scramble control were 5’ and 3’- digoxigenin (DIG) labeled. U6 was used as positive control and labeled at 5’-end only. The experiment was performed according to a company’s protocol. Briefly, tissue slides were deparaffinized and treated with proteinase-K. After that probe hybridization, stringent washes, blocking steps were performed. Finally, slides were treated with anti-DIG reagent, NBT/BCIP substrate (nitro-blue tetrazolium and 5-bromo-4-chloro-3'-indolyphosphate), and nuclear counter staining. The section was mounted with mounting medium and analyzed under the microscopy. The pixel density of miR-21 positive area was determined by ImageJ (https://imagej.nih.gov/ij/) software package.
Statistics
The graphical data were presented as mean ± S.E.M. Statistical significance among the three groups and between groups was determined using one-way or two-way analysis of variance (ANOVA) following Bonferroni post-test and Student’s t-test respectively. Significance was assumed for p < 0.05 (*), p < 0.01 (**), p < 0.001 (***), p < 0.0001 (****).
Results
Local IR exposure mimicking SBRT induces lung fibrosis
The left lungs of mice were exposed to a single IR dose of 90 Gy (X-rays), as described previously [16]. All mice were viable for at least 4 weeks, at which time they were sacrificed and their lungs were harvested. Collagen deposition markedly increased in damaged areas of the left lungs, beginning 2 weeks after IR exposure, suggesting the development of RILF (Fig 1A). The molecular events occurring during RILF were examined by microarray analysis comparing the left and right lungs at each time point (Fig 1A, left panel). Gradual increases in the levels of several collagen subtypes (11A1, 15A1, 24A1, 22A1, 28A1, 10A1, 2A1, 1A1, 1A2 and 3A1) were apparent, beginning 2 weeks after IR exposure, with their levels of expression sustained until sacrifice at 4 weeks (Fig 1B, red dotted box). The gradual deposition of collagens, particularly types Col1A2, Col1A1, Col3A1, Col11A1 and Col15A1, which are commonly increased during fibrosis, beginning 2 weeks after IR exposure, was confirmed by real-time PCR analysis (Fig 1C and S1 Fig).
Upregulation of miR-21 in IR-damaged lung tissue
Recently, miRs whose expression is upregulated in various fibrotic diseases of the skin, kidney, liver and lung were shown to contribute to fibrotic responses [11, 17, 18], suggesting that selective modulation of miRs may be a promising non-steroidal approach to treat fibrosis. miR arrays were prepared from left and right lung tissue samples 3 and 4 weeks after exposing left lungs to IR to identify any miR that may be associated with RILF. Scatter plots of miR expression profiles (cut-off score = 2) at 3 and 4 weeks revealed that the levels of expression of several miRs were significantly altered by IR exposure (S2 Fig). The miRs significantly altered at both time points were subjected to Ingenuity Pathway Analysis (IPA) and mapped to the Ingenuity knowledge database, which incorporates microRNA-mRNA interactions from the databases TarBase, miRecords, and TargetScan, and includes associations of miRs with diseases based on published literature. This analysis indicated that miR-21 and miR-184, which are upregulated in idiopathic pulmonary fibrosis (IPF) [19, 20], were significantly upregulated in IR-injured mouse lung tissue (Fig 2A).
Because miR-21 is involved in fibrosis of multiple tissues, including the lungs [15] and kidneys [21], we focused on miR-21 in IR-injured mouse lungs. Several mRNAs, including those encoding p53, have been shown to interact with miR-21 (S1B Fig) [22, 23]. Real-time RT-PCR analysis confirmed that miR-21 was induced in IR-damaged lung tissue after 3 and 4 weeks (Fig 2B). More importantly, the increased expression of miR-21 in damaged lungs (Fig 2C) strongly correlated with the level of collagen expression (Fig 1B and 1C), a phenotype typical of fibrosis. Monitoring the levels of nine genes, whose expression is regulated by miR-21, in microarrays, showed that several of these target genes, including Spry2, Tpm1, Reck, Bmpr2, Pdcd4 and Smad7 (http://www.genome.jp/kegg-bin/show_pathway?hsa05206), were significantly downregulated at 3 and 4 weeks, at the time of miR-21 induction (Fig 2D). Finally, in situ hybridization showed that miR-21 was markedly increased only at IR-damaged areas (Fig 2E, white circles), suggesting that the local induction of miR-21 in these IR-damaged lung areas may contribute to the progression of pulmonary fibrosis.
IR promotes EndMT in lung ECs concurrent with miR-21 induction
Recent evidence has revealed that fibroblast-like cells, which are responsible for the pathological symptoms of RILF due to the hyper-production of collagens, are derived from pulmonary ECs through EndMT following radiation injury [1, 24]. Therefore, we tested whether miR-21 induction in damaged lung tissue (Fig 2) was associated with EndMT. Human pulmonary microvascular ECs (HPECs) were exposed to IR, inducing EndMT [25], and miR-21 expression was evaluated. IR damage with 5 Gy and 20 Gy doses of X-rays induced the expression of intercellular adhesion molecule 1 (ICAM-1), a marker of IR-induced damage [26, 27], alpha-smooth muscle actin (α-SMA), and fibronectin (FN), all of which are markers of mesenchymal transition (Fig 3A). The reduction in expression of CD31 antigen and the increase in expression of α-SMA in IR-exposed HPECs, accompanied by IR dose-dependent ICAM-1 and p21CIP1 expression, indicated that these HPECs had undergone EndMT (Fig 3B). The cell surface of control HPECs showed predominant arrangements of phalloidin-labeled actin, in tight association with cell-to-cell adhesions and clear morphological changes (Fig 3C) [28]. After IR exposure, these HPECs underwent morphological changes typical of EndMT, such as increased actin reorganization and a loss of VE-cadherin at the cell surface, concurrent with cell-to cell adhesion (Fig 3C) [29]. To confirm that HPECs after EndMT (M-HPECs) acquire mesenchymal properties, collagen production by M-HPECs was determined by real-time RT-PCR. These cells showed marked upregulation of expression of mRNAs encoding collagen types I α2 (Col1A2) and III α1 (Col3A1) (Fig 3D), both of which are also clearly increased in IR-damaged lung tissues (Fig 1B). Moreover, ColA2, Col3A1 and FN mRNAs were increased after HPECs were exposed to 5Gy radiation (S3A Fig). Notably, while M-HPECs displayed mesenchymal properties (Fig 3A, 3B, 3C and 3D), their levels of miR-21 expression were also significantly upregulated, similar to findings in IR-damaged lung tissue, which indicated that miR-21 induction at IR-damaged areas of the lung may contribute to either EndMT or collagen production (Fig 3E and S3B Fig).
miR-21 expression is dispensible for EndMT
The finding that miR-21 was induced in M-HPECs after IR exposure (Fig 3E), similar to results in IR-injured lung tissue (Fig 2), suggests that miR-21 expression in M-HPECs may be important for EndMT. This hypothesis was also supported by results showing that miR-21 contributes in part to TGF-β-induced EndMT [30]. HPECs were therefore treated with anti-sense miR-21 to inhibit miR-21 expression [15], followed by EndMT induction by exposure to IR. Despite the efficient inhibition of miR-21 by anti-sense miR-21, even after IR exposure (Fig 4A), as well as the response to radiation as determined by the induction of ICAM-1 (Fig 4B), the expression of EndMT markers, such as α-SMA, FN (Fig 4C) and ColA2 and ColA3 (Fig 4D), was not affected. Moreover, miR-21 inhibition had no effect on IR-induced morphological changes in HPECs, as shown by increases in stress actin fibers and by losses of VE-cadherin (Fig 4E). Similarly, miR-21 inhibition had no effect on IR-induced reductions in CD31 antigen levels (Fig 4F). To confirm this unexpected observation, miR-21 was overexpressed 150- to 200-fold in HPECs to determine whether this overexpression could convert endothelial-like HPECs to mesenchymal-like cells. This overexpression, however, failed to induce α-SMA (Fig 4G), while moderately reducing FN expression (Fig 4H). These results demonstrated that increased levels of miR-21 are dispensible for EndMT in HPECs.
miR-21 contributes to collagen production in fibroblasts
Because EndMT in HPECs does not require miR-21 overexpression (Fig 4), the role of miR-21 overexpression at IR-damaged sites remains unclear. We therefore tested whether increased miR-21 expression could augment the mesenchymal properties of fibroblast-like cells or fibroblasts after the completion of EndMT in ECs [30] by determining whether miR-21 inhibition alters collagen production in lung fibroblasts. We found that inhibition of miR-21 in MRC-5 human lung fibroblast cells by anti-sense-21 (or miR-21 inhibitor) (Fig 5A) suppressed collagen synthesis (e.g., Col1A2 and Col3A1) at both the mRNA (Fig 5B) and protein (Fig 5C) levels. Collagen synthesis, however, increased after 48 hours, when high cell confluence itself promotes collagen synthesis [31]. In contrast to findings in HPECs (Fig 4F and 4G), the expression of exogenous miR-21 in MRC-5 cells (Fig 5D) enhanced collagen synthesis at both the mRNA (Fig 5E) and protein (Fig 5F) levels in a time-dependent manner. Real-time RT-PCR analysis showed that Smad7 expression was significantly downregulated in IR-injured lung tissues (Fig 5G). Because miR-21-induced Smad7 downregulation contributes to bleomycin-induced pulmonary fibrosis (BLM fibrosis) [15], miR-21 induction in mesenchymal cells may promote the TGF-β gene response by suppressing Smad7. As predicted, expression of exogenous miR-21 alone downregulated Smad7 expression while enhancing Smad2 phosphorylation, resulting in an increase in collagen type III α from COL3A. These findings indicated that expression of exogenous miR-21 activated Smad-dependent TGFβ signaling (S4A and S4B Fig), whereas inhibition of miR21 resulted in a Smad gene response (S4C Fig). These results clearly indicated that IR induction of miR-21 expression primarily contributes to collagen production by fibroblasts or fibroblast-like cells rather than to EndMT in ECs through the downregulation of Smad7.
Discussion
SBRT has been used to treat patients with both primary and metastatic lung tumors [32]. Approximately 9–28% of SBRT-treated lung cancer patients, however, experience radiation-induced pneumonitis (RP), with the extent depending on the radiation dose, tumor grade, and area of normal lung tissue damages [33, 34]. Some patients with RP may progress to RILF, which may be fatal. Whereas the onset of RP occurs 1–6 months after SBRT, RILF takes months to years to develop. Thus, early diagnosis of RILF development is important for initiating anti-fibrotic treatments, such as steroids, which can effectively alleviate RILF symptoms [35–37].
miRs, particularly circulating (or serum) miRs, have been extensively studied to identify biomarkers for certain types of diseases, including cancers [38]. Identifying any miRs that are involved in RILF and that could be readily detected in patients is therefore important. This study found that miR-21 [39], which is expressed in serum, was significantly upregulated in SBRT lung tissue. Additional studies of sera from RILF patients are required to confirm that these miRs are early markers of RILF, similar to findings in patients with IPF [40]. In agreement with results showing that miR-21 is induced in BLM fibrosis [15], this study found that miR-21 levels progressively increased during collagen production at SBRT-damaged sites, accompanied by the significant downregulation of several miR-21 targets, including Smad7, suggesting that increased miR-21 contributes to fibrotic responses. Indeed, miR-21 has been shown to play a role in other fibrotic diseases, including renal [21, 41] and cardiac [42] failure. We therefore tested the ability of an anti-sense oligonucleotide to miR-21, which specifically inhibits miR-21, to delay the fibrotic response, finding that this anti-sense-miR21 was effective [15, 21, 42].
This study also showed that miR-21 induction was concurrent with collagen production at SBRT-damaged sites, promoting collagen production by mesenchymal cells but not by pulmonary ECs. Unlike results showing that miR-21 is partly responsible for TGF-β-mediated EndMT [30], this study found that miR-21 inhibition failed to rescue EndMT progression, with overexpression of exogenous miR-21 having only a slight effect on EndMT in pulmonary ECs. These data suggest that EndMT does not require miR-21 induction by SBRT. The reason for this discrepancy remains unclear, although different stimuli were used to induce EndMT (i.e., TGF-β vs IR) [30]. By contrast, the inhibition or induction of miR-21 affected fibrotic responses only in mesenchymal cells. These results suggest that miR-21, the expression of which is upregulated by a TGF-β-dependent gene response [15, 21], may potentiate fibrotic responses in myofibroblasts and fibroblasts recruited to the damaged areas through suppression of Smad7. Modulation of miR-21 expression by anti-sense-21 would still be a valid approach, as serum levels of miR-21 may increase after SBRT.
Supporting Information
Acknowledgments
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIP) (No. 2009–0093822, 2012055464, and 2015R1D1A3A010178).
Data Availability
All relevant data are within the paper and its Supporting Information files.
Funding Statement
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIP) (No. 2009-0093822 (HJC), 2012055464 (HJC) and 2015R1D1A3A01017832 (JSL)). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
References
- 1.Ding NH, Li JJ, Sun LQ. Molecular mechanisms and treatment of radiation-induced lung fibrosis. Current drug targets. 2013;14(11):1347–56. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Ghafoori P, Marks LB, Vujaskovic Z, Kelsey CR. Radiation-induced lung injury. Assessment, management, and prevention. Oncology. 2008;22(1):37–47; discussion 52–3. . [PubMed] [Google Scholar]
- 3.Martin M, Delanian S, Sivan V, Vozenin-Brotons MC, Reisdorf P, Lawrence D, et al. [Radiation-induced superficial fibrosis and TGF-alpha 1]. Cancer radiotherapie: journal de la Societe francaise de radiotherapie oncologique. 2000;4(5):369–84. . [DOI] [PubMed] [Google Scholar]
- 4.Yarnold J, Brotons MC. Pathogenetic mechanisms in radiation fibrosis. Radiotherapy and oncology: journal of the European Society for Therapeutic Radiology and Oncology. 2010;97(1):149–61. 10.1016/j.radonc.2010.09.002 . [DOI] [PubMed] [Google Scholar]
- 5.Wynn TA. Cellular and molecular mechanisms of fibrosis. The Journal of pathology. 2008;214(2):199–210. 10.1002/path.2277 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Wynn TA, Ramalingam TR. Mechanisms of fibrosis: therapeutic translation for fibrotic disease. Nature medicine. 2012;18(7):1028–40. 10.1038/nm.2807 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Piera-Velazquez S, Jimenez SA. Molecular mechanisms of endothelial to mesenchymal cell transition (EndoMT) in experimentally induced fibrotic diseases. Fibrogenesis & tissue repair. 2012;5(Suppl 1 Proceedings of Fibroproliferative disorders: from biochemical analysis to targeted therapiesPetro E Petrides and David Brenner):S7 10.1186/1755-1536-5-S1-S7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Piera-Velazquez S, Li Z, Jimenez SA. Role of endothelial-mesenchymal transition (EndoMT) in the pathogenesis of fibrotic disorders. The American journal of pathology. 2011;179(3):1074–80. 10.1016/j.ajpath.2011.06.001 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Hashimoto N, Phan SH, Imaizumi K, Matsuo M, Nakashima H, Kawabe T, et al. Endothelial-mesenchymal transition in bleomycin-induced pulmonary fibrosis. American journal of respiratory cell and molecular biology. 2010;43(2):161–72. 10.1165/rcmb.2009-0031OC [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Inui M, Martello G, Piccolo S. MicroRNA control of signal transduction. Nat Rev Mol Cell Biol. 2010;11(4):252–63. 10.1038/nrm2868 . [DOI] [PubMed] [Google Scholar]
- 11.Roderburg C, Luedde T. Circulating microRNAs as markers of liver inflammation, fibrosis and cancer. Journal of hepatology. 2014. 10.1016/j.jhep.2014.07.017 . [DOI] [PubMed] [Google Scholar]
- 12.Chen X, Ba Y, Ma L, Cai X, Yin Y, Wang K, et al. Characterization of microRNAs in serum: a novel class of biomarkers for diagnosis of cancer and other diseases. Cell research. 2008;18(10):997–1006. 10.1038/cr.2008.282 . [DOI] [PubMed] [Google Scholar]
- 13.Huang Y, Shen XJ, Zou Q, Wang SP, Tang SM, Zhang GZ. Biological functions of microRNAs: a review. Journal of physiology and biochemistry. 2011;67(1):129–39. 10.1007/s13105-010-0050-6 . [DOI] [PubMed] [Google Scholar]
- 14.Li Q, Zhang D, Wang Y, Sun P, Hou X, Larner J, et al. MiR-21/Smad 7 signaling determines TGF-beta1-induced CAF formation. Scientific reports. 2013;3:2038 10.1038/srep02038 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Liu G, Friggeri A, Yang Y, Milosevic J, Ding Q, Thannickal VJ, et al. miR-21 mediates fibrogenic activation of pulmonary fibroblasts and lung fibrosis. The Journal of experimental medicine. 2010;207(8):1589–97. 10.1084/jem.20100035 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Hong ZY, Eun SH, Park K, Choi WH, Lee JI, Lee EJ, et al. Development of a small animal model to simulate clinical stereotactic body radiotherapy-induced central and peripheral lung injuries. Journal of radiation research. 2014;55(4):648–57. 10.1093/jrr/rrt234 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Kumar V, Mahato RI. Delivery and Targeting of miRNAs for Treating Liver Fibrosis. Pharmaceutical research. 2014. 10.1007/s11095-014-1497-x . [DOI] [PubMed] [Google Scholar]
- 18.Lv LL, Cao YH, Ni HF, Xu M, Liu D, Liu H, et al. MicroRNA-29c in urinary exosome/microvesicle as a biomarker of renal fibrosis. American journal of physiology Renal physiology. 2013;305(8):F1220–7. 10.1152/ajprenal.00148.2013 . [DOI] [PubMed] [Google Scholar]
- 19.Pandit KV, Milosevic J, Kaminski N. MicroRNAs in idiopathic pulmonary fibrosis. Translational research: the journal of laboratory and clinical medicine. 2011;157(4):191–9. 10.1016/j.trsl.2011.01.012 . [DOI] [PubMed] [Google Scholar]
- 20.Schulz MH, Pandit KV, Lino Cardenas CL, Ambalavanan N, Kaminski N, Bar-Joseph Z. Reconstructing dynamic microRNA-regulated interaction networks. Proceedings of the National Academy of Sciences of the United States of America. 2013;110(39):15686–91. 10.1073/pnas.1303236110 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Zhong X, Chung AC, Chen HY, Meng XM, Lan HY. Smad3-mediated upregulation of miR-21 promotes renal fibrosis. Journal of the American Society of Nephrology: JASN. 2011;22(9):1668–81. 10.1681/ASN.2010111168 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Ma X, Choudhury SN, Hua X, Dai Z, Li Y. Interaction of the oncogenic miR-21 microRNA and the p53 tumor suppressor pathway. Carcinogenesis. 2013;34(6):1216–23. 10.1093/carcin/bgt044 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Papagiannakopoulos T, Shapiro A, Kosik KS. MicroRNA-21 targets a network of key tumor-suppressive pathways in glioblastoma cells. Cancer research. 2008;68(19):8164–72. 10.1158/0008-5472.CAN-08-1305 . [DOI] [PubMed] [Google Scholar]
- 24.Rodemann HP, Bamberg M. Cellular basis of radiation-induced fibrosis. Radiotherapy and oncology: journal of the European Society for Therapeutic Radiology and Oncology. 1995;35(2):83–90. . [DOI] [PubMed] [Google Scholar]
- 25.Kim M, Choi SH, Jin YB, Lee HJ, Ji YH, Kim J, et al. The effect of oxidized low-density lipoprotein (ox-LDL) on radiation-induced endothelial-to-mesenchymal transition. International journal of radiation biology. 2013;89(5):356–63. 10.3109/09553002.2013.763193 . [DOI] [PubMed] [Google Scholar]
- 26.Gaugler MH, Squiban C, van der Meeren A, Bertho JM, Vandamme M, Mouthon MA. Late and persistent up-regulation of intercellular adhesion molecule-1 (ICAM-1) expression by ionizing radiation in human endothelial cells in vitro. International journal of radiation biology. 1997;72(2):201–9. . [DOI] [PubMed] [Google Scholar]
- 27.Behrends U, Peter RU, Hintermeier-Knabe R, Eissner G, Holler E, Bornkamm GW, et al. Ionizing radiation induces human intercellular adhesion molecule-1 in vitro. The Journal of investigative dermatology. 1994;103(5):726–30. . [DOI] [PubMed] [Google Scholar]
- 28.Miettinen PJ, Ebner R, Lopez AR, Derynck R. TGF-beta induced transdifferentiation of mammary epithelial cells to mesenchymal cells: involvement of type I receptors. The Journal of cell biology. 1994;127(6 Pt 2):2021–36. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Andarawewa KL, Erickson AC, Chou WS, Costes SV, Gascard P, Mott JD, et al. Ionizing radiation predisposes nonmalignant human mammary epithelial cells to undergo transforming growth factor beta induced epithelial to mesenchymal transition. Cancer research. 2007;67(18):8662–70. 10.1158/0008-5472.CAN-07-1294 . [DOI] [PubMed] [Google Scholar]
- 30.Kumarswamy R, Volkmann I, Jazbutyte V, Dangwal S, Park DH, Thum T. Transforming growth factor-beta-induced endothelial-to-mesenchymal transition is partly mediated by microRNA-21. Arteriosclerosis, thrombosis, and vascular biology. 2012;32(2):361–9. 10.1161/ATVBAHA.111.234286 . [DOI] [PubMed] [Google Scholar]
- 31.Aumailley M, Krieg T, Razaka G, Muller PK, Bricaud H. Influence of cell density on collagen biosynthesis in fibroblast cultures. The Biochemical journal. 1982;206(3):505–10. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Nagata Y, Negoro Y, Aoki T, Mizowaki T, Takayama K, Kokubo M, et al. Clinical outcomes of 3D conformal hypofractionated single high-dose radiotherapy for one or two lung tumors using a stereotactic body frame. International journal of radiation oncology, biology, physics. 2002;52(4):1041–6. . [DOI] [PubMed] [Google Scholar]
- 33.Ong CL, Palma D, Verbakel WF, Slotman BJ, Senan S. Treatment of large stage I-II lung tumors using stereotactic body radiotherapy (SBRT): planning considerations and early toxicity. Radiotherapy and oncology: journal of the European Society for Therapeutic Radiology and Oncology. 2010;97(3):431–6. 10.1016/j.radonc.2010.10.003 . [DOI] [PubMed] [Google Scholar]
- 34.Stauder MC, Macdonald OK, Olivier KR, Call JA, Lafata K, Mayo CS, et al. Early pulmonary toxicity following lung stereotactic body radiation therapy delivered in consecutive daily fractions. Radiotherapy and oncology: journal of the European Society for Therapeutic Radiology and Oncology. 2011;99(2):166–71. 10.1016/j.radonc.2011.04.002 . [DOI] [PubMed] [Google Scholar]
- 35.Antonadou D, Coliarakis N, Synodinou M, Athanassiou H, Kouveli A, Verigos C, et al. Randomized phase III trial of radiation treatment +/- amifostine in patients with advanced-stage lung cancer. International journal of radiation oncology, biology, physics. 2001;51(4):915–22. . [DOI] [PubMed] [Google Scholar]
- 36.Okunieff P, Augustine E, Hicks JE, Cornelison TL, Altemus RM, Naydich BG, et al. Pentoxifylline in the treatment of radiation-induced fibrosis. Journal of clinical oncology: official journal of the American Society of Clinical Oncology. 2004;22(11):2207–13. 10.1200/JCO.2004.09.101 . [DOI] [PubMed] [Google Scholar]
- 37.Flechsig P, Dadrich M, Bickelhaupt S, Jenne J, Hauser K, Timke C, et al. LY2109761 attenuates radiation-induced pulmonary murine fibrosis via reversal of TGF-beta and BMP-associated proinflammatory and proangiogenic signals. Clinical cancer research: an official journal of the American Association for Cancer Research. 2012;18(13):3616–27. 10.1158/1078-0432.CCR-11-2855 . [DOI] [PubMed] [Google Scholar]
- 38.Mitchell PS, Parkin RK, Kroh EM, Fritz BR, Wyman SK, Pogosova-Agadjanyan EL, et al. Circulating microRNAs as stable blood-based markers for cancer detection. Proceedings of the National Academy of Sciences of the United States of America. 2008;105(30):10513–8. 10.1073/pnas.0804549105 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Xu J, Wu C, Che X, Wang L, Yu D, Zhang T, et al. Circulating microRNAs, miR-21, miR-122, and miR-223, in patients with hepatocellular carcinoma or chronic hepatitis. Molecular carcinogenesis. 2011;50(2):136–42. 10.1002/mc.20712 . [DOI] [PubMed] [Google Scholar]
- 40.Li P, Zhao GQ, Chen TF, Chang JX, Wang HQ, Chen SS, et al. Serum miR-21 and miR-155 expression in idiopathic pulmonary fibrosis. The Journal of asthma: official journal of the Association for the Care of Asthma. 2013;50(9):960–4. 10.3109/02770903.2013.822080 . [DOI] [PubMed] [Google Scholar]
- 41.Chau BN, Xin C, Hartner J, Ren S, Castano AP, Linn G, et al. MicroRNA-21 promotes fibrosis of the kidney by silencing metabolic pathways. Science translational medicine. 2012;4(121):121ra18 10.1126/scitranslmed.3003205 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Thum T, Gross C, Fiedler J, Fischer T, Kissler S, Bussen M, et al. MicroRNA-21 contributes to myocardial disease by stimulating MAP kinase signalling in fibroblasts. Nature. 2008;456(7224):980–4. 10.1038/nature07511 . [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
All relevant data are within the paper and its Supporting Information files.