The occurrence and development of fibrosis is always accompanied with inflammatory response. In liver injury, Kupffer cells firstly cause injury and initiate inflammatory cascade reaction, release a variety of inflammatory factors and secrete CCL2/5 to recruit inflammatory monocytes, macrophages and lymphocytes to the injury site. Macrophages release ASK1, TNF-α and pan-caspase, which further aggravates inflammatory injury. In addition, Kupffer cells also produce cytokines, such as TGF-β₁, PDGF, IL-6 and Gal-3, which promote the activation and proliferation of HSCs. Furthermore, peroxisome proliferators-activated receptors (PPARs), as a kind of regulatory factor against liver fibrosis, are inhibited by activated HSCs, resulting in excessive proliferation and deposition of ECM and the occurrence and development of liver fibrosis (Li and Wang, 2007; Luo et al., 2017). Moreover, chronic liver diseases are generally accompanied by increased de novo lipogenesis (DNL) in the liver (Tamura and Shimomura, 2005; Ameer et al., 2014). Fat is broken down into fatty acids under the action of lipase, and the excessive accumulation of fatty acids in the liver also leads to hepatotoxicity and inflammation (Ameer et al., 2014). Therefore, it is an important measure to prevent liver fibrosis by inhibiting the accumulation of fat in the liver and reducing the secretion of inflammatory cytokines and the release of apoptotic proteins. The research progress of related drugs is summarized in Table 1.

After liver injury, the overproduction of chemokine CCL2/CCL5 is induced in livers of mouse and human, which is related to the severity of liver fibrosis. In the two models of liver fibrosis induced by carbon tetrachloride (CCl₄) and methionine and choline-deficient diet, it was found that Ccl5^–/– mice showed a reduction of HSCs activation, immune cell infiltration and liver fibrosis. Met-CCL5, an antagonist of chemokine (C-C motif) receptor 5 (CCR5), inhibited the migration, proliferation and collagen secretion of HSCs effectively, ameliorated the liver fibrosis in experimental model mice significantly, and accelerated the regression of fibrosis (Berres et al., 2010). Therefore, it is feasible to reduce experimental liver fibrosis by antagonizing CCR5. Cenicriviroc (CVC) is a dual inhibitor of CCR2 and CCR5, and it reduced the amassment and accumulation of pro-inflammatory macrophages in animal models of liver fibrosis (Lefebvre et al., 2016). In a phase II clinical trial (NCT02217475) of NASH patients with liver fibrosis, fibrosis was ameliorated in patients who were administered with 150 mg CVC for 2 years with good safety (Friedman et al., 2016). The results of a phase 2b clinical trial of 289 patients showed that there were twice as many patients with ameliorated fibrosis and no deterioration of steatohepatitis in the 150 mg CVC group as in the placebo group after one-year treatment. The safety and tolerance of CVC were comparable to placebo in Freidman’s research, and the main adverse reactions are fatigue, diarrhea, and headache (Friedman et al., 2018; Tacke, 2018). However, a phase III study (NCT03028740) of patients with advanced fibrosis and cirrhosis, aiming to assess the efficacy and safety of CVC treatment, was terminated recently due to lack of efficacy (Anstee et al., 2020). It reveals that the effectiveness of inhibiting CCR2/CCR5 in the treatment of liver fibrosis still needs more studies to verify.

Overexpression of galactose lectin significantly promoted inflammatory response and aggravated liver fibrosis. Gal-3, as a galactose lectin with immune effects, is secreted by activated Kupffer cells and macrophages in inflammatory state and participates in the pathophysiological process of liver fibrosis (Gudowska et al., 2015; Moon et al., 2018). Belapectin (GR-MD-02), as a Gal-3 inhibitor, is a complex carbohydrate drug, and it was proved to be safe and well tolerated at the maximum dose of 8 mg/kg in phase I clinical trial of NASH patients with advanced fibrosis (Harrison et al., 2016). However, a recent phase 2b multicenter placebo-controlled clinical trial (NCT02462967) of belapectin in patients with liver fibrosis, NASH, and cirrhosis showed that it was tolerated and safe in a dose of 2 mg/kg for 52 weeks compared with placebo, but had no significant effect on reduction of fibrosis or NASH scores. A high proportion of patients in the placebo group and the belapectin group had adverse reactions such as infections and gastrointestinal diseases, with the severity of grade 1 (mild) or grade 2 (moderate). Yet, Chalasani’s research showed that belapectin with dose of 2 mg/kg reduced hepatic venous pressure gradient and variceal development in NASH patients without esophageal varices (Chalasani et al., 2020). In addition, Aspirin, a classic antipyretic and analgesic, was founded that it exerted a significant anti-inflammatory effect by inhibiting IL-6 and TNF-α and reducing the number of inflammatory cells, and it also inhibited the activation and proliferation of HSCs and liver fibrosis via inhibition of toll-like receptor 4 (TLR4)/nuclear factor kappa beta (NF-κB) signal pathway. These results suggested that Aspirin is a potential effective drug for the treatment of liver fibrosis (Liu et al., 2020). IL-1β and IL-1 receptor antagonist (IL-1ra) are important mediators of chronic liver disease. IL-1ra treatment had a certain anti-fibrotic effect in the bile duct ligation-induced (BDL) mouse model of hepatic fibrosis, but it had a pro-fibrotic effect in the CCl₄-induced mouse model of hepatic fibrosis (Meier et al., 2019). This suggests that blocking IL-1-mediated inflammation may only be selectively beneficial to liver fibrosis.

De novo lipogenesis plays a major role in fatty acid metabolism and is a necessary link for HSCs activation. The first step of the synthesis of DNL is catalyzed by acetyl-CoA carboxylase (ACC) as the rate-limiting enzyme. It has been reported that the inhibition of ACC decreased liver steatosis and serum fibrosis biomarkers in patients with NASH, depressed the pro-fibrotic activity of HSCs, and reduced the severe degree of liver fibrosis in diethylnitrosamine (DMN) chemical-induced liver injury model and high fat diet-induced rat model (Ross et al., 2020). An ACC small molecule inhibitor, GS-0976, was used in a phase II randomized placebo-controlled trial (NCT02856555) of 126 NASH patients with F1–F3 fibrosis. The results showed that the fibrosis marker TIMP1 declined in a dose-dependent manner in the patients who were administered 20 mg/d GS-0976 for 12 weeks, accompanied by 30% decrease in liver fat and depression of liver injury markers, but there was no change in liver hardness. In addition, GS-0976 was safe, but the plasma triglyceride level was > 500 mg/dL observed in 16 patients, which may cause atherosclerosis (Loomba et al., 2018a). The effects of GS-0976 on cardiovascular function need long-term studies to determine. The novel ACC1/2 inhibitor WZ66 was reported that it significantly improved NASH-related liver function by reducing steatosis, triglycerides and other lipids, and inhibiting the activation of Kupffer cells and HSCs in high fat diet-induced mice model (Gao et al., 2020).

Glucagon-like peptide-1 (GLP-1) directly ameliorated the state of liver fibrosis by increasing insulin release, reducing glucagon secretion, decreasing the concentration of liver enzymes and depressing hepatic steatosis. The GLP-1 analog liraglutide was carried out in a phase II randomized placebo-controlled trial (NCT01237119) of 52 patients with NASH. The liver biopsy results showed that 39% of patients with continuous administration of 1.8 mg/d liraglutide for 48 weeks had definite non-alcoholic steatohepatitis improvement without further exacerbation of liver fibrosis, while only 9% of patients in the placebo group had improvement. Furthermore, only 9% of patients in the liraglutide group had further fibrosis compared with 36% in the placebo group. Safety and tolerability of liraglutide were comparable to placebo, and the main adverse events of liraglutide group are gastrointestinal disorders, nausea and diarrhea with the severity of grade 1 or grade 2 (Armstrong et al., 2016). Resmetirom (MGL-3196) is a selective thyroid hormone receptor β agonist with oral activity, which aims to improve NASH by increasing liver fat metabolism and reducing lipo-toxicity. The results of a 36-week multicenter randomized double-blind placebo-controlled trial (NCT02912260) of 348 patients showed that resmetirom decreased liver fat content by 32.9% and 37.3%, respectively, after 12 weeks and 36 weeks treatment with a dose of 80 mg in patients with F1–F3 fibrosis, compared with 10.4% and 8.5% in the placebo group. Moreover, most adverse events were mild or moderate, such as diarrhea and nausea (Harrison et al., 2019).

Oxidative stress is an important factor in liver injury and liver fibrosis. Oxidative stress reaction (ROS) produces excessive reactive oxygen species and active free radicals in the liver, which weakens the antioxidant function and causes the increase of active free radicals in hepatocytes, the decrease of scavenging, and the destruction of hepatocyte membrane. These results affect the function of synthesis and degradation of hepatocytes, and lead to hepatocyte necrosis and apoptosis. In addition, ROS also promotes the activation of HSCs and liver fibrosis by causing peroxidation damage to Kupffer cells and neutrophils, up-regulating the gene expression of collagen type I alpha 2 in the liver, and triggering inflammation (Schwabe and Brenner, 2006; Yang et al., 2017).

Up to now, the common anti-oxidative stress and hepatocyte protection drugs include reduced glutathione, tiopronin, silymarin, s-allylcysteine (SAC), oroxylin A, methyl ferulic acid (MFA) and so on. Reduced glutathione protects the hepatocyte membrane from the damage of active free radicals by accelerating the scavenging of free radicals. Tiopronin can not only scavenge free radicals, but also promote hepatocyte regeneration. Silymarin, as a classical drug for repairing liver injury, inhibits the formation of lipid peroxide and stabilizes liver cell membrane. Also, it has the effects of protecting liver and anti-liver fibrosis. SAC inhibited the fibrosis process and improved the survival rate of rats with CCl₄-induced liver fibrosis in a dose-dependent manner. Its therapeutic effect is better than that of N-acetylcysteine (Kodai et al., 2015). Therefore, SAC is expected to become an effective drug for the treatment of liver fibrosis. RAP-8 showed anti-fibrotic effect by inhibiting oxidative stress and promoting cell cycle arrest (Xu et al., 2019). Oroxylin A effectively alleviated liver fibrosis by clearing ROS, suppressing phosphatidylinositol 3-kinase (PI3K)/AKT/mTOR signal transduction, and inhibiting the secretion of pro-inflammatory cytokines in activated HSCs (Shen et al., 2020). MFA, a bioactive monomer, has a protective effect on liver injury. And it inhibited liver fibrosis in CCl₄-induced rats by inhibiting TGF-β₁/Smad and NADPH oxidase 4 (NOX4)/ROS signal pathways, down-regulating the level of procollagen type III, collagen type IV and laminin, up-regulating the ratio of MMP2/TIMP1, and inhibiting the synthesis of ECM and the activation of HSCs (Cheng et al., 2019).

Nicotinamide adenine dinucleotide phosphate (NADPH) oxidase (NOX) is a multicomponent transmembrane enzyme complex, including six subtypes of NOX1, NOX3, NOX4, NOX5, DUOX1 and DUOX2. When the cells are subjected to stimulation, NOX receives the signal to produce ROS, and then causes oxidative damage. The key cells in the liver to produce NOX are Kupffer cells and HSCs. Kupffer cells produce only NOX2, while HSCs produces NOX1, NOX 2 and NOX 4. In the process of hepatic fibrosis, NOX1, NOX 2 and NOX 4 play a key role in HSCs activation, proliferation and ECM synthesis, and NOX4 is involved in hepatocyte apoptosis (De Minicis and Brenner, 2007; Mortezaee, 2018). As a dual NOX1/4 inhibitor, GKT137831 reduced the production of ROS in HSCs both in vitro and in vivo. It significantly inhibited the formation of hepatic fibrosis and hepatocyte apoptosis in prevention or treatment groups in mice models of hepatic fibrosis induced by CCl₄ and BDL (Aoyama et al., 2012; Jiang et al., 2012). Currently, GKT137831 is undergoing a fibrotic effect trial (NCT03226067) on patients with primary cholangitis after 24 weeks of treatment, which expected to have a satisfactory feedback. Angiotensin II (Ang II) promoted fibrosis by phosphorylating non-phagocytic NOX regulatory subunit p47 phox and inducing oxidative stress. Losartan, as an Ang II receptor blocker, ameliorated inflammation and fibrosis in 50% of the patients who were administered with 50 mg/d for 18 months in a clinical trial of 14 HCV patients with liver fibrosis (Colmenero et al., 2009). However, there is a lack of control study in this trial, and the reliability of the results needs to be further confirmed.

In the process of hepatic fibrosis, hepatocyte death and apoptosis are the main influencing factors of inflammation and HSCs activation. Dead hepatocytes release DAMPs to activate HSCs and Kupffer cells. Hepatocyte apoptosis activated Fas death receptor, which induced the release of apoptotic bodies, and finally leaded to fibrogenic response (Mihm, 2018). In addition, phagocytosis of apoptotic cells activated HSCs (Witek et al., 2009). Therefore, the inhibition of hepatocyte apoptosis is beneficial to inhibit inflammation, prevent the activation of HSCs and reduce liver fibrosis.

Whether it is endogenous or exogenous apoptosis pathway, the last common step of hepatocyte apoptosis is carried out by a family of cysteine-proteases termed caspases. Pan-caspase promoted apoptosis by activating apoptotic protease. Pan-caspase inhibitor VX-166 inhibited hepatocyte apoptosis, decreased hepatic steatosis, and postponed the process of fibrosis in NASH mice model, but didn’t cause significant improvement in liver injury (Witek et al., 2009). Emricasan, a small molecule pan-caspase inhibitor, significantly ameliorated liver injury and fibrosis in NASH mice model by inhibiting caspase activity and reducing hepatocyte apoptosis, ameliorating inflammatory environment and inhibiting HSCs activation (Barreyro et al., 2015). Moreover, Emricasan dramatically ameliorated fibrosis, portal hypertension and liver function by improving hepatic sinusoidal microvascular dysfunction in rats with advanced liver cirrhosis induced by CCl₄ (Gracia-Sancho et al., 2019). Emricasan also improved liver function of patients with severe liver cirrhosis with good safety, tolerance and similar adverse reactions compared with placebo group in a 3-month multicenter phase II randomized clinical trial (NCT02230670) of 74 patients with liver cirrhosis. The new or worsening decompensation event in the placebo group was mainly ascites, while that in the emricasan group was mainly hepatic encephalopathy, which was generally caused by the patient’s original disease (Frenette et al., 2019). However, emricasan did not improve liver inflammation or fibrosis in NASH patients with F1–F3 fibrosis who received 72 weeks of 5 mg/d or 50 mg/d treatment (NCT02686762), but may cause more severe liver fibrosis and hepatocyte swelling, which due to the activation of other cell death or necrosis mechanisms (Harrison et al., 2020a).

Tumor necrosis factor alpha participates in the activation and expression of apoptotic ligand. Its inhibitor pentoxifylline prevented porcine serum-induced liver fibrosis in rats by inhibiting the production of IL-6 and the proliferation of HSCs. In addition, pentoxifylline decreased the inflammatory state, reduced oxidative stress and ameliorated the degree of liver fibrosis in patients with NASH by inhibiting the transcription of TNF-α gene, but it had no significant effect on patients with alcoholic hepatitis (Toda et al., 2009). A study showed that β-elemene prevented hepatic fibrosis by down-regulating the expression of serum TNF-α and liver CD14 and decreasing plasma endotoxin in CCl₄-induced hepatic fibrosis rats (Liu et al., 2011).

Another way to reduce hepatocyte death associated with liver injury is to suppress stress signals. ASK1, which is activated by a variety of pro-fibrotic factors, activates MAPK signal pathway, and participates in hepatocyte apoptosis, inflammation and fibrosis. Selonsertib (GS-4997), a selective ASK1 inhibitor, inhibited HSCs proliferation and ECM production by blocking the ASK1/MAPK pathway, and significantly alleviated DMN-induced liver fibrosis in rats (Yoon et al., 2020). Selonsertib was used to treat 74 NASH patients with F2–F3 fibrosis for 24 weeks with dose of 6 mg/d or 18 mg/d in a multicenter phase II clinical trial. The results demonstrated that selonsertib decreased fibrosis-related markers and biomarkers in the process of apoptosis, reduced inflammatory levels, and ameliorated hepatic fibrosis. Most patients have experienced mild or moderate adverse reactions, such as headache, nausea and rhinitis. In addition, three patients in the selonsertib group discontinued treatment due to serious adverse reactions (Loomba et al., 2018b; Harrison et al., 2020c). Moreover, the results need to be confirmed by further studies, because the placebo control group was not included in this study. Yet, selonsertib had no anti-fibrotic effect on NASH patients with F3 or F4 fibrosis after 48 weeks treatment with dose of 6 mg/d or 18 mg/d in a phase III clinical trial (NCT03053050; NCT03053063) (Harrison et al., 2020c).

Tumor necrosis factor-β₁ is a vital profibrotic cytokine in the development of liver fibrosis. The up-regulation of TGF-β₁/Smad signal pathway is one of the most important factors in the process of liver fibrosis. During liver injury, TGF-β₁ binds to the type II receptor on HSCs, which recruits and activates type I receptor via phosphorylation of serine residues. The activated type I receptor activates receptor-regulated protein Smad2/3 via re-phosphorylation, which separates from the receptor and forms a complex with Smad4. The complex trans-locates to the nucleus and down-regulates the expression of Smad7, which inhibits TGF-β₁ by negative feedback, regulates the expression of fibrosis-related genes and induces the activation, proliferation and trans-differentiation of HSC into myofibroblasts, promotes the excessive synthesis and deposition of ECM and finally aggravates fibrosis (Derynck and Zhang, 2003). Therefore, the inhibition of TGF-β₁/Smad signal pathway plays a critical role in inhibiting the activation and proliferation of HSCs and ameliorating liver fibrosis.

Pirfenidone (PFD) is a broad-spectrum anti-fibrotic drug, which was approved by FDA in 2014 for the treatment of idiopathic pulmonary fibrosis. Preclinical studies showed that PFD effectively ameliorated the liver inflammation and fibrosis induced by concanavalin A, CCl₄ and BDL in mice by significantly reducing the level of serum TGF-β₁ and collagen expression (Garcia et al., 2002; Seniutkin et al., 2018; Salah et al., 2019). At present, the study of PFD against liver fibrosis has entered phase II clinical trials. The results of treating 22 patients with HCV infection showed that PFD significantly ameliorated liver fibrosis in 67% of the patients with continuous administration for 2 years by significantly decreasing TGF-β₁ levels and ameliorating inflammation, steatosis and liver function. The adverse events are mild, such as gastritis and nausea (Flores-Contreras et al., 2014). Yet, because of no placebo control group in this study, further research is needed to confirm these results. In addition, a clinical study (NCT04099407) of prolonged-release formulation pirfenidone (PR-PFD) showed that it significantly reduced fibrosis in 35% of the 122 patients who had advanced liver fibrosis with different chronic liver injury diseases and were treated for one year, by decreasing levels of TGF-β₁ and improving liver function, while there was only 4.1% in non-PR-PFD group. Moreover, only 12% patients had transient burning or nausea and 7% patients had photosensitivity, indicating that PR-PFD had good safety in advanced liver fibrosis (Poo et al., 2020). Therefore, PR-PFD is a potential candidate drug for anti-fibrosis. The me-better drug of PFD, Fluorofenidone, alleviated liver fibrosis and liver injury induced by porcine serum in rats through reducing the activation of HSCs induced by TGF-β₁ and inhibiting TGF-β_1/Smad and MAPK signal pathways (Peng et al., 2019). Furthermore, praziquantel, as a schistosomicide with good safety, significantly alleviated liver fibrosis induced by CCl₄ in mice by up-regulating the expression of Smad7 in HSCs, inhibiting TGF-β₁/Smad signal pathway, inhibiting the activation of HSCs and reducing collagen production (Liu et al., 2019). In addition, ferulic acid effectively improved hepatic fibrosis in vivo and in vitro by inhibiting the expression of α-SMA, collagen, fibronectin and other fibrosis markers in human HSC line LX2 induced by TGF-β₁, inhibiting the protein levels of p-Smad2 and p-Smad3 in CCl₄-induced hepatic fibrosis model, and inhibiting TGF-β₁/Smad signal pathway (Mu et al., 2018).

Although inhibiting TGF-β₁/Smad signal pathway is challenging for liver fibrosis, it still has pros and cons. TGF-β₁/Smad signal pathway is crucial to maintain liver immune homeostasis through its anti-inflammatory nature and growth regulatory function. TGF-β₁ inhibits the activation of macrophages and expression of inflammatory factors, such as TNF-α and MMP-12, in a manner that depends on smad3, which balances the immune microenvironment (Li et al., 2006). It has been reported that the levels of TGF-β₁ on patients with null-mild liver fibrosis are higher than those with advanced liver fibrosis, which hint that TGF-β₁ may exert an anti-fibrotic effect through its anti-inflammatory activity and immune regulatory functions, as the improvement of liver inflammation can improve liver fibrosis in patients (Rallón et al., 2011). In addition, TGF-β₁ regulates the proliferation, differentiation, survival and functions of various immune cells, such as T lymphocytes, B lymphocytes, dendritic cells, and macrophages. Since those immune cells play an important role in mediating liver homeostasis (Li et al., 2006), blocking TGF-β₁ may lead to disorders of liver homeostasis. Therefore, it is crucial to focus on how to balance the relationship between the pro-fibrotic activity, anti-inflammatory activity and functions of maintaining liver homeostasis of TGF-β₁/Smad.

Platelet derived growth factor is an important mitogen in the differentiation of HSCs. During liver injury, Kupffer cells mediate platelet recruitment in the liver and produce a large number of PDGF. In addition, endothelial cells and activated HSCs also express PDGF. The binding of PDGF to its receptor (PDGFR) induces dimerization and phosphorylation of the receptor, which in turn phosphorylates tyrosine residues on different substrates in the cell. These results regulate the expression level of fibro-genic target genes, such as collagen type I alpha 1 (COL1a1), TIMPs, MMPs and apoptosis regulatory factor B cell lymphoma/lewkmia 2 (Bcl2), which leads to the survival and proliferation of HSCs (Borkham-Kamphorst and Weiskirchen, 2016). Stimulation of PDGFR activates several signal pathways, including Ras/extracellular signal-regulated protein kinase/MAPK pathway, PI3K/AKT pathway, Janus kinase/signal transducer and transcriptional activator (STAT) pathway. Moreover, PDGFR mRNA deletion in hepatocytes inhibited the up-regulation of PDGFR mRNA expression in HSCs, decreased activation of HSCs and alleviated liver fibrosis (Lim et al., 2018). Therefore, the inhibition of PDGFR is useful to inhibit the proliferation of HSCs and alleviate liver fibrosis.

A study founded that sorafenib up-regulated the expression of Fas, Fas-L and Caspase-3 by inhibiting PDFGR and VEGFR2, decreased the ratio of Bcl2 to Bcl2-related protein x (Bax), inhibited the proliferation of HSCs, promoted apoptosis of HSCs, reduced collagen accumulation, and alleviated liver fibrosis (Wang et al., 2010; Sung et al., 2018). However, another study founded that although sorafenib inhibited the levels of PDFGR and p-AKT when HSCs were treated with low-dose sorafenib with sub-micromolar concentration, it still induced the activation of MAPK in HSCs and promoted the differentiation of myofibroblasts. Sorafenib and MEK inhibitor AZD6244 jointly inhibited the contradictory activation of MAPK and HSCs in vitro through chemokine (C-X-C motif) receptor 4-targeted nanoparticles delivery, and alleviated liver fibrosis in liver injury model induced by CCl₄ in mice (Sung et al., 2018). Nilotinib, an inhibitor of tyrosine kinase, down-regulated the level of pro-fibrosis cytokines by reducing the expression of PDGFR and the level of TGF-β₁, and significantly reduced CCl₄-induced hepatic fibrosis in rats (Shiha et al., 2014). Dihydroartemisinin promoted the activation of caspase cascade in HSCs, up-regulated Bax, and down-regulated Bcl, suppressed PI3K/AKT pathway, inhibited proliferation of HSCs and induced its apoptosis, improved liver tissue structure, and ameliorated liver fibrosis induced by BDL in rats (Chen et al., 2016). Asiatic acid inhibited the activation of HSCs and the synthesis of ECM by reducing oxidative stress, inflammation and hepatocyte apoptosis, and inhibited PI3K/AKT/mTOR signal pathway, which effectively improved CCl₄-induced liver injury and fibrosis in rats (Wei et al., 2018). Rilpivirine (RPV) is an anti-HIV drug with no hepatotoxicity reported. It reduced collagen expression in vitro, and had obvious anti-inflammatory and anti-fibrosis effects in NAFLD model and rat model of liver fibrosis induced by CCl₄ and BDL. Through selective activation of STAT1, RPV promoted STAT3-dependent hepatocyte proliferation and HSCs apoptosis, and had bystander effects on hepatocytes, which promoted liver regeneration and ameliorated liver fibrosis (Marti-Rodrigo et al., 2020).

Connective tissue growth factor is an important pro-fibrotic factor in the process of fibrosis, and is induced by TGF-β₁. It promotes the production of ECM and enhances the proliferation, migration and survival ability of activated HSCs, which promotes the occurrence and development of liver fibrosis in different liver chronic diseases (Kovalenko et al., 2009).

It has been reported that pioglitazone inhibited the development of liver fibrosis by inhibiting the expression of CTGF and type III collagen in HSCs and preventing the morphological changes of HSCs induced by TGF-β₁ in a dose-dependent manner (Jia et al., 2007). Curcumin ameliorated fibrosis by inhibiting the expression of CTGF, preventing the activation of HSCs in vitro, and reducing the synthesis of ECM (Chen and Zheng, 2008). Moreover, basic studies have shown that CTGF small interfering RNA (siRNA) significantly inhibited the expression of CTGF, type I collagen, type III collagen and hyaluronic acid, reduced the synthesis and secretion of ECM, alleviated liver fibrosis and protected liver function (Li et al., 2004). Additionally, Src family kinases (SFKs), as non-receptor tyrosine kinases, were activated by CTGF induced by TGF-β₁ and had an essential effect on transcription of CTGF (Zhang et al., 2010). The expression of Src kinases is up-regulated in mice with liver fibrosis and cirrhosis induced by thioacetamide (TAA), and the expression of phosphorylated Src kinases is up-regulated when HSC is activated. Saracatinib, an inhibitor of Src kinases, attenuated the expression of type I collagen, CTGF and α-SMA in mice induced by TAA. What’s more, inhibition of Src kinases increased autophagy flux and reduced liver fibrosis (Seo et al., 2020). SU6656, a dual inhibitor of Src family and Aurora kinases, reduced CTGF expression by inhibiting Src kinases in non-transformed epithelial cells (Cicha et al., 2014). As a member of SFK, Fyn was activated in the liver of patients with fibrosis and knockdown Fyn with siRNA or gene knockout significantly prevented the activation of HSCs and reduced fibrosis in CCl₄-induced mice. Saracatinib treatment decreased the activation of Fyn, prevented the activation of HSCs, and depressed the severity of liver fibrosis in mice induced by CCl₄ (Du et al., 2020).

There are several isoforms in the Fibroblast Growth Factor (FGF) family, which bind to four different receptors (FGFR1-4). Among them, FGF15/19 and FGF21 could inhibit the occurrence of liver fibrosis by down-regulating HSCs activation. In addition, FGFR1-mediated signal transduction is closely related to hepatic fibrosis and liver cirrhosis. FGF21 inhibits the activation of HSCs by down-regulating the expression of TGF-β₁, decreasing the phosphorylation level of Smad2/3 and reducing the nuclear translocation of NF-κB. FGF21 also induces apoptosis of activated HSCs by increasing the expression of caspase 3 and decreasing the ratio of Bcl2 to Bax (Xu et al., 2016).

Pegbelfermin (BMS-986036) is a polyethylene glycol modified FGF21 analog. In a multicenter double-blind phase 2a clinical trial (NCT02413372), 75 NASH patients with F1–F3 fibrosis were treated with 10 mg or 20 mg pegbelfermin once a day for 16 weeks. The results showed that the absolute liver fat fraction in the pegbelfermin group was much lower than that in the placebo group, and most of the adverse events were mild, such as ascites and varicose, indicating that pegbelfermin ameliorated NASH, steatosis, liver injury and fibrosis (Sanyal et al., 2019a; Verzijl et al., 2020). FGF19 is a hormone that regulates the synthesis of bile acids directly in the liver. The engineered FGF19 analog NGM282 was injected subcutaneously with 3 mg or 6 mg to 82 patients with F1–F3 fibrosis for 12 weeks in a randomized, double-blind, placebo-controlled phase II clinical trial (NCT02443116). The results indicated that the absolute liver fat contents were at least 5% lower than the baseline in 20 patients (74%) in the 3 mg group and 22 (79%) patients in the 6 mg group while in only 2 patients (7%) in the placebo group (Harrison et al., 2018). This study demonstrated that NGM282 played a positive role in improving the condition of patients with NASH. In another open label study, NGM282 with 1 mg or 3 mg administration for 12 weeks improved the histological characteristics of NASH, reduced fibrosis-related markers significantly, decreased NASH and fibrosis scores, and ameliorated fibrosis effectively. And the most common adverse reactions are mild or moderate abdominal pain, diarrhea and nausea (Harrison et al., 2020b). The FGFR1 inhibitor hydronidone improved the inflammation and fibrosis in rats with hepatic fibrosis induced by CCl₄, DMN and human serum albumin. Hydronidone was well tolerated with no obvious adverse reaction in phase II clinical trial (NCT02499562), but its absorption rate and degree decreased via food intake (Liu et al., 2017).

Studies have shown that Wnt/β-catenin signal pathway is related to the activation of HSCs and hepatic fibrosis. Wnt protein forms a ternary complex with frizzled receptor and lipoprotein receptor-related protein (LRP)-5/6, which blocks the degradation of β-catenin. β-catenin is activated with the help of coactivators such as cyclic-AMP response element binding protein binding protein (CBP), and then accumulates and easily locates in the nucleus, which activates the transcription of related target genes (Ge et al., 2014). During liver injury, Wnt/β-catenin signal pathway is abnormally activated in activated HSCs and alleviates liver fibrosis by promoting collagen deposition and epithelial-mesenchymal transition (EMT) (Nishikawa et al., 2018).

ICG001 is a small molecular inhibitor that disrupts the interaction between CBP and β-catenin. ICG001 reduced the secretion of CCL12 and prevented the infiltration of macrophages by inhibiting the Wnt/β-catenin signal pathway in HSCs, which reduced liver inflammation and significantly decreased the activation of HSCs and the accumulation of ECM in liver fibrosis model induced by CCl₄ in mice (Akcora et al., 2018). CBP/β-catenin inhibitor PRI-724 improved HCV-induced liver fibrosis in mice by inhibiting the activation of HSCs (Tokunaga et al., 2017). In a single-center phase I clinical trial (NCT02195440), PRI-724 was well tolerated in HCV cirrhotic patients who were given 10 mg/d or 40 mg/d within 12 weeks. However, severe liver injury may occur in cirrhotic patients with HCV given 160 mg/d PRI-724 (Kimura et al., 2017). At present, a phase 1/2a clinical trial (NCT03620474) of PRI-724 in patients with hepatitis B or hepatitis C-related liver cirrhosis is under way, which is expected to have some implications for the study of PRI-724 in liver fibrosis. Octreotide is an analog of somatostatin. It significantly inhibited the expression of Wnt1 and β-catenin in vitro and in vivo, depressed the activation and proliferation of LX2 and reduced CCl₄-induced liver fibrosis in rats (Zhang et al., 2018). These findings provide more options for the treatment of liver fibrosis.

Farnesoid-X receptor (FXR) is an inherent inhibitor of apoptosis in hepatocytes. It interacts with caspase-8 in the cytoplasm, prevents the formation of death-induced signal complex and the activation of caspase-8, mediates the inhibition of HSCs activation and ameliorates liver fibrosis (Wang et al., 2018). Some studies found that the lack of FXR aggravated liver fibrosis and inflammation in mice, indicating that FXR played a key role in protecting the liver from inflammation and fibrosis (Ferrell et al., 2019). Obviously, FXR is a very important anti-fibrosis target.

Farnesoid-X receptor agonist obeticholic acid (OCA, INT-747) is a semisynthetic chenodeoxycholic acid, which has good anti-fibrotic activity in animal model of liver fibrosis (Goto et al., 2018; Fan et al., 2019). In 2015, a double-blind, randomized placebo-controlled phase 2b clinical trial of 283 NASH patients showed that liver histology improved significantly in 45% patients after 72 weeks of short-term 25 mg/d OCA treatment, compared with 21% in the placebo group. But 23% patients in the OCA group had adverse reactions such as itching, compared with only 6% in the placebo group. These results indicate that the safety of OCA needs further research to determine (Neuschwander-Tetri et al., 2015). Recently, the mid-term results of the first 18 months of a multicenter, randomized placebo-controlled phase III clinical trial (NCT02548351) of 931 NASH patients with F2–F3 fibrosis who received long-term treatment with OCA showed that 23% of the patients in the 25 mg OCA group had a significant improvement on the severe degree of fibrosis and NASH in a dose-dependent manner, compared with 12% in the placebo group. And the most common adverse reaction was pruritus (Younossi et al., 2019). Cilofexor (GS-9674) is a small non-steroidal agonist of FXR. In a double-blind placebo-controlled phase II clinical trial (NCT02854605), 140 patients with NASH were administered with 30 mg or 100 mg cilofexor for 24 weeks. The results showed that cilofexor significantly reduced hepatic steatosis and serum bile acid in NASH patients and was well tolerated. Moderate to severe itching was more common in the 100 mg cilofexor group (14%) than that in the 30 mg group (4%) and the placebo group (4%) (Patel et al., 2020). In another study, FXR agonist PX20606 effectively improved liver fibrosis in CCl₄-induced cirrhotic rats by reducing the expression of collagen (Schwabl et al., 2017).

Endogenous cannabinoid system is involved in the pathogenesis of liver fibrosis. In normal liver, the expression of cannabinoid receptor is very low. However, in ALD, NAFLD, liver regeneration/injury, liver fibrosis/cirrhosis and liver cancer, cannabinoid receptor 1 (CB1), a kind of G protein-coupled receptor, is up-regulated in liver myofibroblasts due to extracellular stimulation, which promotes the development of liver fibrosis (Teixeira-Clerc et al., 2006; Bataller and Gao, 2013). Therefore, blocking the CB1 signal pathway is expected to become a new strategy to treat a variety of liver diseases including liver fibrosis.

Rimonaban, a CB1 receptor (CB1R) antagonist, significantly reduced inflammation and fibrosis in CCl₄-induced cirrhotic rats by down-regulating the expression of fibrosis and inflammation-related genes. It showed that even in the late stage of the disease, pharmacological CB1 antagonism still had a positive effect on the regression of fibrosis (Giannone et al., 2012). Another CB1R antagonist SR141716A effectively alleviated hepatic fibrosis in three chronic liver injury models by inhibiting CB1 to decrease the expression of TGF-β₁ and prevent the accumulation of fibrogenic cells in the liver (Teixeira-Clerc et al., 2006). JD5037 is a peripheral CB1 antagonist. It attenuated CB1R-regulated activation of HSCs and liver fibrosis by inhibiting CB1R-arrestin1/AKT signal pathway, as CB1R, which were induced in liver sections of patients and mice with hepatic fibrosis, promoted the activation of HSCs by recruiting beta arrestin1 and activating AKT signal pathway. Therefore, JD5037 is a potential compound for anti-hepatic fibrosis (Tan et al., 2020).

Peroxisome proliferators-activated receptors are a family of nuclear receptors, including PPAR-α, PPAR-β/δ and PPAR-γ. PPAR-α is a critical regulatory factor against hepatic fibrosis. PPAR-γ negatively regulates the activity of HSCs in hepatic fibrosis and reduces the differentiation of myofibroblasts (Wei et al., 2019).

Elafibranor (GFT-505) is a PPAR-α/δ agonist. In a randomized placebo-controlled phase II clinical trial (NCT01694849) involving 276 patients with NASH, the results of continuous treatment with 120 mg elafibranor for 52 weeks indicated that elafibranor ameliorated liver fibrosis and liver function while improving the NASH status of the patients, and was well tolerated. However, in the intended treatment, there was no significant difference between the elafibranor group and the placebo group. Elafibranor caused a slight and reversible increase in creatinine levels, but it did not cause adverse effects on patients with renal insufficiency (Ratziu et al., 2016). Rosiglitazone, a PPAR-γ agonist, improved BDL-induced liver fibrosis in mice by regulating NF-κB-TNF-α pathway in a PPAR-γ-dependent manner, down-regulating the expression of TGF-β₁, α-SMA and type I collagen, inhibiting NF-κB phosphorylation, and alleviating inflammation, but it did not alleviate liver injury in Hep Ppar-γ KO mice (Wei et al., 2019). 15-d-PGJ2 (PPAR-γ natural ligand) or GW7845 (synthetic ligand) significantly promoted the transformation of TGF-β₁-induced activated HSCs to quiescent phenotype by inhibiting PPAR-γ-dependent CTGF expression at both mRNA and protein levels in HSCs (Sun et al., 2009). Crocin, a naturally occurring carotenoid, was reported that it ameliorated CCl₄-induced hepatic fibrosis in a dose-dependent manner by up-regulating the expression of PPAR-γ and down-regulating the expression of inflammatory and hepatic fibrosis-related factors (Chhimwal et al., 2020).

Statins are HMG-CoA reductase inhibitors, which reduce serum cholesterol levels by inhibiting the activity of HMG-CoA reductase. The effects of statins on reducing liver inflammation, oxidative stress and fibrosis have been reported in several studies on animal models of liver fibrosis (Oberti et al., 1997; Jang et al., 2018). Yet, the safety of statins in patients with chronic liver disease and cirrhosis needs to be evaluated in further research, considering that statins may increase the risk of rhabdomyolysis due to impaired liver CYP3A4 metabolism. Moreover, a study reported that 3% of cirrhotic patients who were administrated with statins had severe rhabdomyolysis (Abraldes et al., 2009). Currently, three placebo-controlled trials about statins (NCT03780673; NCT02968810; NCT04072601) are under way with an extended safety assessment.

Dipeptidyl peptidase-4 is a serine protease widely expressed on various cell surfaces, which has an influence on fibronectin-mediated interaction between hepatocytes and ECM, and participates in the adhesion of cells to collagen. In addition, DPP4 is expressed on the surface of activated HSCs. It has been reported that the DPP4 inhibitor sitagliptin ameliorated NAFLD (Iwasaki et al., 2011). Alogliptin, which is a classical DPP4 inhibitor, inhibited the activation of LX2 induced by TGF-β₁ stimulation in vitro. Chronic treatment with alogliptin reduced hepatic steatosis in mice and protected them from liver injury in the hepatic fibrosis model induced by CCl₄, which delayed the progression of hepatic fibrosis. Alogliptin also had a positive effect on ameliorating liver fibrosis via the negative regulation of HSCs activation (Zhang et al., 2019). This indicates that alogliptin is also a potential candidate drug for treatment of liver fibrosis.

Matrix metalloproteinases/TIMPs are important enzymes that regulate the deposition and degradation of ECM. MMPs are the main ECM-degrading enzyme in the liver and their endogenous inhibitors are TIMPs. MMP2 and MMP14 are highly expressed in activated HSCs. MMPs degrade ECM under normal circumstances. But with liver injury, MMPs are inhibited by TIMPs, which are high expressed. This causes the break of the balance between deposition and degradation of ECM, which leads to excessive deposition of ECM and eventually leads to liver fibrosis (Iredale et al., 2013). Therefore, up-regulation of MMPs or down-regulation of TIMPs activity is an effective measure to alleviate liver fibrosis.

Halofuginone, a small molecular derivative of quinolones, inhibited the expression and synthesis of collagen, reduced the level of TIMPs and alleviated hepatic fibrosis in rats induced by TAA and Con A (Bruck et al., 2001; Liang et al., 2013). It has been reported that Fraxinus rhynchophylla ethanol extract (FR(EtOH)) had an anti-fibrosis effect in CCl₄-induced liver fibrosis in SD rats. FR(EtOH) effectively alleviated liver lesions and fibrous connective tissue proliferation by down-regulating the expression of MMP2, MMP9 and TIMP1 (Peng et al., 2010). As the main composition of ECM is type I and III collagen after liver injury and type I collagen is the most abundant collagen in fibrotic liver, inhibition type I or III collagen production and accumulation will be beneficial to the treatment of liver fibrosis. It has been reported that liposome COL1a1 siRNA specifically inhibited collagen production and accumulation in liver fibrosis model in mice (Jimenez et al., 2015). Hsp47, a kind of type I collagen molecular chaperone, has the ability to block collagen synthesis. Furthermore, Hsp47 siRNA containing vitamin A-coupled liposomes had significant anti-fibrosis effect in three liver fibrosis models in vivo (Sato et al., 2008). BMS986263, a kind of Hsp47 siRNA, which delivered lipid nanoparticles, did not show any toxicity to healthy people (Kavita et al., 2019). And its phase Ib/2 dose increment study (NCT02227459) has been completed recently.

The Lysyl oxidase (LOX) family promotes the deposition of ECM by increasing the cross-linking of collagen. Therefore, inhibiting the LOX family is beneficial to reduce the deposition of ECM and alleviate liver fibrosis.

Simtuzumab (GS-6624), an antibody of lysyl oxidase-like protein 2 (LOXL2), decreased the stability of ECM by antagonizing the collagen cross-linking induced by LOXL2, and had a good therapeutic effect on liver cirrhosis and fibrosis induced by NASH. Moreover, simtuzumab was well tolerated in a 22-week phase II clinical trial (NCT01707472) of 18 patients with advanced fibrosis. The most common adverse reactions of simtuzumab treatment are fever, headache, glossitis, etc., which are mild. In addition, one patient experienced a serious adverse reaction and recovered after antibiotic treatment (Meissner et al., 2016). However, a phase Ib clinical trial (NCT01672853) of 234 patients showed that simtuzumab had no effect on preventing the progression of liver fibrosis in patients with primary sclerosing cholangitis with a dose of 75 mg or 125 mg for 96 weeks (Sanyal et al., 2019b). In addition, A study showed that the expression of LOXL2 decreased rapidly after liver injury compared with the stable up-regulation of LOX and LOXL1, indicating that LOXL2 had little effect in liver fibrosis (Perepelyuk et al., 2013). Future research should solve this problem of selectivity by specifically targeting LOX1.