A narrative review of the role of necroptosis in liver disease: a double-edged sword

Abstract

Acute and chronic liver injuries lead to hepatocyte death and turnover. When injuries become chronic, continuous cell death and transformation lead to chronic inflammation, fibrosis, cirrhosis, and eventually carcinoma. A therapeutic strategy of great significance for liver disease is to control hepatocyte death in acute and chronic injuries. This strategy prevents hepatocytes from causing liver failure and inhibits both secondary inflammation and fibrosis. Both apoptosis and necrosis have been proven to occur in the liver, but the role of necroptosis in liver diseases is controversial. Necroptosis, which has features of necrosis and apoptosis, is a regulatory process that occurs in some cell types when caspases are inhibited. The signaling pathway of necroptosis is characterized by the activation of receptor-interacting proteins kinase (RIPK) and mixed lineage kinase domain-like (MLKL). Necroptosis is associated with a variety of inflammatory diseases and has been the focus of research in recent years. The incidence of necroptosis in liver tissues has been studied recently in several liver injury models, but the results of the studies are not consistent. The purpose of this review is to summarize the published data on the involvement of necroptosis in liver injury, focusing on the controversies, issues remaining to be discussed, and potential therapeutic applications in this area.

Introduction

Liver disease is a major reason for illness and death worldwide. The burden of liver diseases in China is primarily due to viral hepatitis, nonalcoholic fatty liver disease, and alcoholic liver disease (1). Although many preventative measures have been adopted over the years, the number of patients with alcoholic and nonalcoholic fatty liver diseases is still increasing rapidly. Liver cancer is one of the most fatal cancers in the world and the second-most common cancer in China. The prognosis of hepatocellular carcinoma (HCC) is extremely poor due to its insidious onset, invasiveness, aggressiveness, high recurrence rate, and fatality. The HCC 5-year average survival rate is less than 10% (2). Liver disease remains a major threat to public health, human health, and quality of life.

Necroptosis is a newly discovered pathway of regulated necrosis that is mediated by receptor-interacting proteins kinase 1 and 3 (RIPK1, RIPK3) and MLKL (3-5). It is induced by death receptors, interferons, toll-like receptors (TLRs), intracellular RNA and DNA sensors, and probably other mediators as well (6). Typically, necroptosis is regarded as a pro-inflammatory mode of cell death that releases intracellular components. However, many studies have shown that necroptosis may have anti-inflammatory effects by blocking the excessive production of chemokines (7,8). It has already been shown that RIPKs are involved in multiple pathophysiologies, and the inhibition of these kinases could have therapeutic potentials (9,10). However, the contribution of caspase-independent RIPK3 and MLKL to hepatocyte necroptosis remains debatable (11). However, it has become evident that, other than apoptosis, necroptosis is also a highly relevant form of programmed cell death (PCD) in the liver (12). The minimal expression of a key player involved in necroptosis in the liver suggests that it may be uncommon in liver diseases (13). In order to find new and effective targets for the treatment of liver diseases, it is essential to understand the role of necroptosis at different stages of liver disease to develop new therapeutic approaches. In this review, we summarize the recent progress in identifying the role of necroptosis in the pathogenesis of liver diseases. We present the following article in accordance with the Narrative Review reporting checklist (available at http://dx.doi.org/10.21037/atm-20-5162).

Characteristics and classical signaling pathway of necroptosis

Necrosis and apoptosis are well-established forms of cell death, that occurs through various physiological and pathological processes. In addition to these, many new means of cell death have been discovered and characterized, including necroptosis, pyroptosis, and ferroptosis. Necroptosis first came to light in 1996 and was officially termed in 2005 (14,15). Many factors contribute to necroptosis, such as microbial infections and physicochemical stressors. However, no specific necroptotic damage-associated molecular patterns (DAMPs) have been found (10). Necroptosis is a genetically programmed and caspase-independent form of cell death (16). The signaling molecules that are considered to be responsible for the activation of necroptosis are RIPK1, RIPK3, and MLKL (17-19). Necroptosis, pyroptosis, and apoptosis share components of a common signaling pathway. Morphologically, necroptosis is similar to necrosis. It is characterized by cellular and organelle swelling, membrane damage, and release of intracellular contents, which all contribute to inflammatory reactions in lesion areas (20,21).

The tumor necrosis factor (TNF) and TNF receptor 1 (TNFR1)-mediated signaling pathway is one of the most extensively studied models of necroptosis (22). It is prevalent in different types of tumors and other pathophysiological conditions (23). This classical signaling pathway is initiated by the binding of the TNF ligand to its receptor TNFR1, which coalesce and provide a binding site for TNFR1-associated death domain protein (TRADD) and the polyubiquitinated receptor-interacting protein 1 (RIP1). After RIP1 is deubiquitinated by cylindromatosis (CYLD), caspase 8, RIP1, RIP3, and Fas-associated protein with death domain (FADD) form complex IIa. Apoptosis occurs when caspase 8 is activated. When the activity of caspase 8 is inhibited (such as through zVAD), RIP1 and RIP3 do not separate from each other and form a necrosome (complex IIb). The necrosome, composed of RIP1, RIP3, and MLKL, is phosphorylated in a step-wise manner. Phosphorylated MLKL is then transported into the nucleus and plasma membrane, triggering membrane punctures and cell rupture, and thereby leading to necroptosis (24,25). Despite the critical role of RIP1 in necroptosis, and researches suggest that there are RIP1-independent necroptosis pathways. It has been shown that virus-induced necroptosis depends on the DNA-dependent activator interferon-regulatory factor (DAI) and RIP3, independent of RIP1 function (26). Furthermore, interferons (IFNs) can also trigger necroptosis independent of RIP1 via the interferon-induced protein kinase PKR (27). The above relevant signal pathway has been shown in Figure 1. In addition, RIP1 kinase does not contribute to TRIF-dependent necroptosis in some kind of cell types apart from macrophages (26). Multiple molecular inhibitors have emerged as requirements of initiation of necroptosis. Necrostatins, including Nec-1 and Nec-2, inhibit RIPK1; kinase inhibitors, including GSKʹ840, GSKʹ843, and GSKʹ872, inhibit RIPK1 and RIPK3; and necrosulfonamide (NSA) inhibits MLKL (28). In addition, several natural products and isolated compounds, such as curcumin and kongensin A, were found to have an inhibitory effect on necroptosis (12).

Figure 1.

The classical necroptosis signaling pathway initiated by the combining of TNF ligand and TNF receptor 1. The combination of TNF α and TNF receptor 1 can induce necroptosis, when the caspase-8 activity is inhibited. The binding between RIP1, RIP3 and MLKL induces the phosphorylation of MLKL and subsequent execution of necroptosis. In addition, IFNs also trigger necroptosis independently of RIPK1 via the interferon-induced protein kinase PKR. Toll receptor and DAI can activate RIPK3 independent of RIPK1.

Recently, necroptosis has emerged as a critical pathway underlying human diseases (29-31), such as breast cancer (32), acetaminophen-induced-liver injury (33), autoimmune disease, and autoinflammatory disease (29).

Current strategies to detect necroptosis in the liver

Typically, the activation of RIP1, RIP3 and MLKL causes the occurrence of necroptosis. Despite their potential use as markers, there is still no highly specific test for the immunohistochemical detection of necroptosis (34). Although western blotting seems to be relatively specific and reliable for the evaluation of RIPK3 expression, the activation of this pathway in parenchymal cells and non-parenchymal cells cannot be clearly distinguished through western blotting (34). The antibodies for p-MLKL are not sensitive enough to detect a subtle activation of MLKL in hepatocytes or livers [for instance in mouse nonalcoholic steatohepatitis (NASH) models]. Furthermore, the phosphorylation of MLKL does not necessarily indicate necroptotic cell death, because MLKL can self-phosphorylate. RIPK1/3 have multiple function apart from mediator of necroptosis (35,36). Another marker we have used to detect necroptosis is p-RIPK1. Several autophosphorylation sites of RIP1 have been identified in in vitro kinase assays, including Ser14/15, Ser20, Ser161, and Ser166. Anti-phospho-RIP1 antibodies have been developed as makers for the activation of RIP1, which can specifically recognize the phospho-Ser166 and phospho-Ser14/15 of hRIP1 (34). However, both apoptosis and necroptosis are detected because RIPK1 is involved in both signaling pathways (11). Hence, the accurate detection and recognition of necroptosis is difficult. Nevertheless, there are other possible methods to detect necroptosis. For instance, necrosome assembly and RIP3-MLKL have been shown to interact through co-immunoprecipitation experiments or microscopically using the DuoLink^® proximity ligation assay (37-39). The aggregation status of RIP3 and MLKL can also be monitored by evaluating their retention in insoluble/soluble protein fractions, or by co-staining of thioflavin T, a β-amyloid fibril marker, with RIP3 puncta (40-42).

Thus, definitive identification of necroptosis requires affirmation by different detection methods and by detection of several kinds of signaling molecular, such as combining the biochemical and morphological tests. Up to now, immunohistochemistry and western blot analyses for phosphor-MLKL are considered acceptable methods to detect necroptosis (41,43).

Necroptosis as a potential target for the treatment of liver disease

Recently, the pathophysiological role of necroptosis has been highlighted in inflammatory diseases and it has become an attractive target for the treatment of liver diseases (40). As RIPK3 is more specific to necroptosis, it is believed that cells that do not express RIPK3 do not undergo necroptosis. The occurrence of necroptosis in the liver and its contribution to liver diseases is debated. Because RIPK3 is difficult to be detected in hepatocytes under basal conditions (44). Additionally, evidence has shown that RIPK3 is predominantly expressed in non-parenchymal cell fractions (non-LPCs) (45). Accordingly, some researchers believe that cholangiocytes can undergo necroptosis, while primary hepatocytes die exclusively by apoptosis after treating with cell death-inducing stimuli in vitro (45). Other research proved that caspase 8 competent wild-type hepatocytes express RIPK3 at low levels compared with many other cell types, but it is sufficient to trigger necroptosis and inflammation when caspase 8 is depleted from hepatocytes in the livers of mice in vivo (12). Further, RIPK3 has been detected in liver biopsies of NASH patients, as well as in the liver of mice exposed to diets deficient in methyl-choline or high in fat, suggesting a role of necroptosis in the pathogenesis of non-alcoholic fatty liver disease (NAFLD)/NASH (46). Moreover, in human patients, necroptosis is activated in alcoholic liver injuries, which are the leading causes of liver cirrhosis and HCC in the western world (47,48). Research shows that RIPK3 mRNA levels in peripheral blood mononuclear cells (PBMCs) are linked to poor prognosis of acute‐on‐chronic hepatitis B liver failure (ACHBLF), thus necroptosis is proposed to play a critical role in the pathogenesis of ACHBLF (49). While the transcription of MLKL was very low in healthy controls, MLKL expression in hepatocytes of AIH patients, in patients with steatosis, and patients with primary biliary cirrhosis was strongly upregulated (50). When infected by Listeria monocytogenes, Kupffer cells residing in the liver underwent necroptotic cell death, which therefore balances type 1 microbicidal inflammation and type-2-mediated liver repair upon infection (51). According to a relevant study, RIPK3 is involved in cytokine production of liver leukocytes after being stimulated by α-galactosylceramide (α-GalCer) (52). Furthermore, acidic extracellular pH (pHe) switches TNF-related apoptosis-inducing ligand (TRAIL)-induced apoptosis to necroptosis in human HT29 and HepG2 cells (53).

We conclude that in order for primary hepatocytes to execute necroptosis, an additional sensitization step is required. It is possible that under pathological conditions, augmented levels of RIPK3 or MLKL switch apoptosis to necroptosis in cells with low expression of these key necroptotic proteins. Furthermore, important functions of necroptosis might exist in other cell types, such as biliary cells, hepatic stellate cells, Kupffer cells or endothelial cells (12,51). In summary, necroptosis plays a critical role in liver diseases.

The role of necroptosis is still incompletely defined in hepatitis, cirrhosis, and liver cancer

Acute liver failure is characterized by massive loss of parenchymal cells but is usually followed by restitution and integrum (12,50). By contrast, in chronic liver diseases, hepatocytes degenerate, necrose, and regenerate. Meanwhile, fibrous tissues proliferate and repair, ultimately leading to cirrhosis and HCC. Necroptosis takes place during hepatic regeneration, inflammation and fibrogenesis in the hepatic disease condition (54). To gain a deeper understanding of the relationship between necroptosis and liver diseases, we review on the role of necroptosis at different stages of liver diseases.

Necroptosis promotes inflammation in acute liver disease

Acute liver inflammation is usually induced by bacterial infection or physical and chemical injury. It is reported that higher necroptosis of hepatocytes emerged in Gal-3 deficient mice in acute CMV-induced liver disease (55). In patients suffering from drug-induced liver injury (DILI), cell death was demonstrated to be associated with activation of MLKL (56). In fact, there are many controversies arising from the use of acetaminophen (APAP)-overdosed mouse models. Generally, we believe that inhibition of RIP1 or RIP3 can alleviate APAP-induced acute liver injury, but the role of MLKL in APAP-induced acute liver injury is still uncertain (57-60). In immune mediated acute liver injury models, such as those induced by concanavalin A (Con-A) and α-GalCer, Sib-RIPK1 inhibitor protects mice from Con A-induced hepatitis (61). Nec-1was found to reduce liver cell death and alleviate liver damage in Fmr1^null mice following TNF exposure. Deletion of RIPK3 delays hepatic injury induced by Con-A (58). Consistent with these findings, increased pathology after bile duct ligation coincided with increased hepatic expression of RIPK1, RIPK3 and p-MLKL (41,62,63). Similarly, pretreatment with Nec-1 or RIPK3 deletion protect against ConA and α-GalCer induced liver injury (44). This protection against ConA-induced liver injury is associated with down-regulated hepatocyte-specific IL-33 expression. It should be noted that IL-33 is a classical DAMP that is tightly linked to necrosis or necroptosis (64). Apart from this, deletion of RIPK3 and pharmacological inhibition of dynamin related protein 1 (Drp1) protect mice from natural killer T (NKT) cell-mediated induction of acute liver damage. Jouan-Lanhouet et al. suggest that use of pharmacological inhibitors of RIPKs could be a new strategy for treatment of immune-mediated hepatitis (53). These findings suggest that necroptosis may promote inflammation in acute liver injury.

However, mice expressing a form of RIPK1 lacking kinase activity were protected, whereas deletion of RIPK1 in hepatocytes aggravated ConA-induced liver injury. Even, it is reported that Nec-1 severely exacerbated ConA-induced disease and mice with ablation of RIPK3 were not protected (58). Combining reports that RIPK3 has also been suggested to regulate NKT cell function and promote the NKT cell mediated anti-tumor immune response through a process that is independent of the necroptosis pathway (52). Apart from this, it is suggested that different components of the necrosome must be considered independently to analyze their opposite effect on damage (58). The protective function of RIPKs was not confirmed in conditional, hepatocyte-specific RIPKs knockout mice. Collectively, RIPKs may have other important functions independent of their actions as cell death mediators, and their role in acute liver injury remains poorly understood (20,44). It is reported that RIPK3 can promote NLRP3 inflammasome and IL-1β inflammatory responses independent of MLKL and necroptotic cell death (65). Furthermore, in addition to causing necroptosis by rupturing the membrane, MLKL controls the transport of endocytosed proteins, thereby enhancing the degradation of receptors and ligands. Thus, the extracellular release of phosphorylated MLKL within vesicles serves as a mechanism for self-restricting the necroptotic activity of this protein (66). Wong et al. showed that RIPK1 and RIPK3 can facilitate the production of multiple cytokines, independent of their role in necroptosis (67). They further found that the kinase activities of RIPK1 and RIPK3, in addition to their roles in regulating necroptosis, have a physiological role in the tumor microenvironment, in particular tumor cell extravasation and remodeling by altering the downstream signaling pathways of permeability factors (68).

Inhibiting necroptosis can alleviate chronic liver disease and cirrhosis

Chronic liver inflammation (CLI), a complex process, exhibits progressive destruction and regeneration of liver parenchymal cells (LPCs). There are a multitude of reasons for CLI, such as viral infection, alcohol abuse, drug toxicity, and genetic metabolic disorders (69). Chronic pathologic processes mainly include viral infection, alcoholic liver disease (ALD), NASH, and autoimmune diseases, which lead to liver cirrhosis and ultimately HCC (69). Hepatocytes suffer a variety of forms of death including apoptosis, necrosis and necroptosis during the CLI progression. In recent years, several studies have shown that RIPK3-dependent necroptosis is an important pathway that regulates fibrosis progression (12,70-73).

It was reported that the inflammation and liver pathology decreased in vaccinia virus-infected RIPK3-deficient mice with altered TNFα-induced necroptosis (74). Moreover, mice infected by vaccinia virus can present the accumulation of the RIPK1/RIPK3 complex in liver (39); both of these results indicate that necroptosis participates in the process of viral infection of the liver. Hepatitis B virus (HBV) and hepatitis C virus (HCV) are well known as leading causes of liver cirrhosis and HCC (75). The effect of HCV on hepatocyte cell death might be prevented in vitro by inhibitors of apoptosis and necroptosis (76). Moreover, Han et al. showed that RIPK3 mRNA levels were significantly higher in patients with ACHBLF. RIPK3 and MLKL were negativity regulated by caspase-8, which was positively correlated with liver injury and poor prognosis (49). They concluded that necroptosis might play an important role in the pathogenesis of this disease.

Chronic alcohol consumption can lead to ALD, which is characterized by steatosis, inflammation, fibrosis, and cirrhosis, and may even cause liver cancer (47). ALD, which features excessive hepatocyte death and inflammation, is a prevalent disease that causes a heavy health burden worldwide. Some studies revealed that hepatocyte necroptosis is a central event that promotes inflammation in ALD (77). Roychowdhury et al. indicated that RIPK3 expression was increased in ethanol-fed mouse livers and in ALD patients’ livers. Furthermore, RIPK3-mediated necroptosis is highly correlated with poor prognosis in patients with alcoholic cirrhosis (38,72). Accordingly, ethanol-induced liver injury, steatosis, and inflammation were decreased in RIP3 knockout mice compared to control mice (38). We can conclude that RIPK3 is important in mediating ethanol-induced liver injury and progression of ALD.

With regard to hepatocyte cell death in NASH, apoptosis was regarded as the key driver by most studies. Apoptosis was detected in both liver tissues from patients with NASH and in commonly used mouse models of NASH. However, Gautheron et al. confirmed that blockage of necroptosis via ablation of RIPK3 protected mice from NASH-induced liver fibrosis, and they deduced that necroptosis rather than apoptosis controls liver fibrosis (71). They could not detect the activation of apoptosis in the liver of mice fed with methionine-choline-deficient (MCD), and western blotting showed that RIPK3 expression in this model was strongly up-regulated (40). Similarly, patients with NASH had a dramatic upregulation of hepatic RIPK3 expression as an indicator of necroptosis, suggesting a shift away from apoptotic towards necroptotic signaling in the livers of these patients (40). More importantly, in the MCD NASH mouse model, injury and fibrosis indicated that the main role of caspase-8 in NASH was to prevent the over-activation of necroptosis. By contrast, inhibition of RIPK3 in the MCD NASH model ameliorated liver injury and fibrosis, providing evidence that necroptosis, not apoptosis, is the driver of liver injury and liver fibrosis in this well-established mouse model of NASH. Along with these findings in mice, a western blot analysis of frozen liver tissue from a cohort of patients with biopsy-proven NASH, showed that these patients had lower levels of intrahepatic caspase 3 cleavage than healthy individuals. In a genetic model of chronic hepatic inflammation, chronic inflammation induced by LPC-specific deletion of tumor growth factor‐β‐activated kinase‐1 (Tak1), RIPK3-dependent necroptosis represents a pathway. This pathway regulates the consequences of chronic inflammation in the liver by counteracting against caspase 8-dependent compensatory proliferation of hepatocytes, immune cell activation, hepatic fibrogenesis, and the development of chromosomal aberrations leading to hepatocarcinogenesis (78).

NAFLD is the initial stage of NASH, often contributing ultimately to liver fibrosis and liver cancer (71). Studies indicate that necroptosis is a key pathogenic event in human and experimental murine models of non-alcoholic steatohepatitis (40). RIPA-56 was regarded as a highly specific and metabolically stable inhibitor of RIPK1 (79). In a newly published study, Majdi et al. showed that RIPA-56 significantly reduced all liver features associated with steatohepatitis, including inflammation and liver fibrosis, in mice with high fat diet (HFD) and hepatocytes from patients with NAFLD (80). They also suggested that necroptosis contributed to the pathogenesis of NAFLD, and that the release of RIPK1 and MLKL into systemic circulation reflects necro-inflammatory activity in human NAFLD. Furthermore, MLKL but not RIPK3 contributes to Western diet-induced liver injury and a murine model of non-alcohol-associated fatty liver and steatohepatitis through inhibition of autophagy and induction of necroptosis (81,82). Even the expression of RIPK3 was upregulated in mice with hepatic steatosis induced by HFD. However, previous reports about the role of RIPK3 in HFD are controversial (83,84). RIP3 deficiency protects from liver disease in MCD-fed mice (40,71), whereas deletion of RIP3 exacerbates liver damage and steatosis, and glucose intolerance induced by a high-fat diet (83). These conflicting results may be due to different modeling methods. Compared with liver injury induced by HFD, mice on MCD diet will show more severe lipidosis, fibrosis, and more active oxidative stress. At the same time, there are differences in modeling performance with different fat composition and proportions (85,86). Furthermore, these data imply that RIP1 and RIP3 cannot be simply considered part of a single functional unit. Indeed, much of the literature in acute liver injury is hindered by conflicting reports between laboratories (58).

In a liver fibrosis model induced by CCl₄, CCl₄ significantly increased RIPK1 expression, the formation of the RIPK1 and RIPK3 necrosome complex, and the level of MLKL protein in liver tissue, all of which were attenuated by MLT (87). This finding suggested that MLT may prevent liver fibrosis by inhibiting necroptosis-associated inflammatory signaling. A study showed that curcumol protects mice liver from CCl₄-induced injury and ameliorates murine hepatic fibrogenesis. The researchers investigated further and eventually found that curcumol reduces the expression of pro-fibrotic proteins by inducing RIPK1/RIPK3-mediated necroptosis in hematopoietic stem cells (HSCs). They also investigated knockdown of RIPK3 in HSCs and found that the effect of curcumol on attenuating hepatic fibrosis was impaired (73). Above all, necroptosis seems to play a positive role in the procession of fibrosis. In the meantime, other studies determined that caspase 8 was negatively correlated with liver fibrosis (63). To be specific, mice lacking the NLRP3 inflammasome had reduced liver fibrosis following CCL₄ or thioacetamide treatment. Meanwhile, caspase 8 can inhibit the NLRP3 inflammasome. The activity of caspase 8 was inhibited when necroptosis started. Above all, we can deduce that liver fibrosis would accelerate when necroptosis occurs and necroptosis may be a basic factor in the pathogenesis of CLI. However, the relative potency of necroptosis to trigger CLI remains ill-defined.

Caspase inhibitors are an attractive therapy for fibrotic liver disease

Since necroptosis, which can be induced by inhibiting caspase-8 activity, plays an important role in chronic liver diseases, some investigations were focused on caspases inhibitors. For instance, VX-166, an inhibitor of caspase, was used to inhibit apoptosis, which could significantly reduce liver damage and fibrosis, whereas it had no effect on the ALT/AST in the MCD model of NASH (88). In addition, the oral administration of the caspase inhibitor GS-9450 (an inhibition of caspases 1, 8, and 9) and emricasan resulted in a decrease in alanine transaminase and α-SMA levels in patients with NASH (89). Pan-caspase inhibitor IDN-6556 reduced the development of bile duct ligation-induced liver fibrosis (54). Despite that fact, emricasan treatment did not achieve the primary objective of ameliorating fibrosis in a large-scale randomized trial in NASH patients (90). These data demonstrate that caspase inhibitors may be an attractive antifibrotic therapy in NASH. However, is the protective effect of caspase inhibitors convincing? Is the protective effect of caspase inhibitors caused by necroptosis? The answers to these questions are still unclear. For faster development of a new strategy for liver disease treatment, the underlying mechanisms need further study.

Necroptosis exerts both pro- and anti-tumoral effects during liver cancer

HCC is the prevailing histological type of liver cancer, comprising approximately 80% of cases (91,92). Cell death is a fundamental driver of liver diseases progression and the development of HCC (35). In tumors, tumor cells can usually evade apoptosis through a selection process (54). The step when parenchymal liver cells (hepatocytes and cholangiocytes) become insensitive to apoptotic cell death, is essential for malignant transformation. It should be noted that most human hepatoma cell lines such as Huh-7, HepG2, and Hep3B present a methylation-dependent loss of RIPK3 expression and thereby suppress the initiation of necroptosis, which indicates that escape from necroptosis is a similarly vital part in the malignant transformation of HCC. Furthermore, recovery of RIPK3 expression by demethylation of its promoter can restore the sensitivity of cell lines to chemotherapy, showing that regulating necroptosis may be an effective way to enhance the chemosensitivity of HCC, a tumor that generally is not responsive to traditional chemotherapy. The strategy of triggering necroptosis in cancer therapy shows great potential (21). Therefore, necroptosis can prevent tumor development when apoptosis fails to be induced. However, necroptosis can induce inflammatory responses and reportedly promotes cancer metastasis and immunosuppression. Additionally, even the same oncogenic driver will instigate different liver cancers, due to the different hepatic microenvironment. Aberrantly activated hepatocytes transformed into cholangiocarcinoma when embedded in a necroptosis-dominant hepatic microenvironment (93).

microRNAs (miRNAs or miRs) comprise a group of small noncoding RNAs that participate in cell proliferation, differentiation, apoptosis, and necroptosis (94,95). The dysregulation of miRNAs has often been observed in HCC (96). The expression levels of Linc00176 is correlated both with the differentiation grade in primary HCCs and with the survival time of HCC patients by titrating tumor suppressor microRNAs. Linc00176-depleted HepG2 cells experience necroptosis rather than apoptosis, as MLKL was detected in these cells (97). In addition, a study identified a novel three-miRNA signature, comprising miR-371-5p, miR-373 and miR-543, that appeared to orchestrate PCN in HCC by directly targeting the caspase-8 gene (Casp-8) (98). Hence, some kinds of miRNAs can modulate the process of tumorigenesis by way of necroptosis.

Collectively, increasing experimental evidence suggests that necroptosis pathways play critical roles in hepatocarcinogenesis, but the precise mechanism is less clear and still needs to be explored.

Conclusions

As a newly defined form of cell death, doubts still remain about the occurrence and role of necroptosis. Typically, the upregulation of RIPK1, RIPK3 and MLKL present the occurrence of necroptosis. However, detection of these molecular signals underlying necroptosis is somewhat difficult and has low specificity. There still are many controversies regarding this process that need to be addressed. However, the identification of necroptosis has changed our understanding about cell death and liver diseases. Based on current literature, it seems that necroptosis can play a vital role in different stages of liver disease. Since there are many challenges to clearly distinguish between necrosis, apoptosis, and necroptosis, it is necessary to find more specific canonical molecular signals in necroptosis to aid in its verification from different aspect. Moreover, it is recommended that further studies should focus on the role of necroptosis in different liver cells, including hepatocytes, cholangiocytes, and immune cells. Additionally, despite the unsatisfactory clinical trial results, pharmacological inhibition of RIPK1 emerges as a potential therapeutic method to cure chronic liver disease and HCC. Given that the role of RIPKs changes under different conditions, it is vital to clarify the underlying mechanism of necroptosis in different kinds of liver diseases. Furthermore, the contribution of RIPK3/MLKL remains debatable (11). Therefore, the effects of RIPK1, RIPK3, and MLKL should be studied separately and in greater detail. Most importantly, more specific downstream signaling molecules involved in necroptosis need to be detected.

Supplementary

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