Liver Fibrosis: Molecular Pathogenesis and Therapeutic Interventions

Jiaorong Qu , Wenqing Qin , Minghang Dong , Zhi Ma , Si Li , Runping Liu , Ranyun Chen , Changmeng Li , Xiaojiaoyang Li

MedComm ›› 2026, Vol. 7 ›› Issue (5) : e70750

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MedComm ›› 2026, Vol. 7 ›› Issue (5) :e70750 DOI: 10.1002/mco2.70750
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Liver Fibrosis: Molecular Pathogenesis and Therapeutic Interventions
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Abstract

Liver fibrosis is a common pathological process, leading to the development of end-stage liver diseases. It is triggered by various etiological drivers including viral hepatitis, metabolic-associated steatotic liver disease (MASLD), and cholestasis. Given the substantial impact of liver fibrosis on individuals and its associated mortality rates, effective management of this condition is crucial for improving public health. Despite a growing number of preclinical studies and clinical trials, a systematic synthesis remains lacking. In this review, the molecular panorama of liver fibrogenesis is summarized at first, encompassing etiological drivers of chronic liver injury, key cellular players, core signaling pathways, and extracellular matrix dynamics. Therapeutic interventions in preclinical or clinical stages are systematically classified into two main categories: etiological treatment as the foundational approach and mechanism-based antifibrotic therapies. Emerging and future therapeutic strategies, including those targeting gut–liver axis, gut microbiota, and cell-based therapies, are also addressed along with inherent challenges. Furthermore, future perspectives centered on precision medicine, combination therapies, novel target discovery, and advanced drug delivery systems are emphasized. This review offers a comprehensive overview of the etiologies, diagnostic approaches, pathogenic mechanisms, current development of antifibrotic agents, and prospects for future therapeutic directions of liver fibrosis.

Keywords

drug therapy / etiological treatment / future therapeutic directions / liver fibrosis / pathogenic mechanisms

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Jiaorong Qu, Wenqing Qin, Minghang Dong, Zhi Ma, Si Li, Runping Liu, Ranyun Chen, Changmeng Li, Xiaojiaoyang Li. Liver Fibrosis: Molecular Pathogenesis and Therapeutic Interventions. MedComm, 2026, 7 (5) : e70750 DOI:10.1002/mco2.70750

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References

[1]

Moon, A. G. Singal, and E. B. Tapper, “Contemporary Epidemiology of Chronic Liver Disease and Cirrhosis,” Clinical Gastroenterology and Hepatology 18, no. 12 (2020): 2650–2666.

[2]

S. O'Reilly, “Epigenetics in Fibrosis,” Molecular Aspects of Medicine 54 (2017): 89–102.

[3]

T. Xue, X. Qiu, H. Liu, et al., “Epigenetic Regulation in Fibrosis Progress,” Pharmacological Research 173 (2021): 105910.

[4]

M. Parola and M. Pinzani, “Liver Fibrosis: Pathophysiology, Pathogenetic Targets and Clinical Iss Ues,” Molecular Aspects of Medicine 65 (2019): 37–55.

[5]

H. Devarbhavi, S. K. Asrani, J. P. Arab, Y. A. Nartey, E. Pose, and P. S. Kamath, “Global Burden of Liver Disease: 2023 Update,” Journal of Hepatology 79, no. 2 (2023): 516–537.

[6]

T. Kisseleva and D. Brenner, “Molecular and Cellular Mechanisms of Liver Fibrosis and Its Regression,” Nature Reviews Gastroenterology & Hepatology 18, no. 3 (2021): 151–166.

[7]

C. Trautwein, S. L. Friedman, D. Schuppan, and M. Pinzani, “Hepatic Fibrosis: Concept to Treatment,” Journal of Hepatology 62, no. 1 Suppl (2015): S15–24.

[8]

T. Tsuchida and S. L. Friedman, “Mechanisms of Hepatic Stellate Cell Activation,” Nature Reviews Gastroenterology & Hepatology 14, no. 7 (2017): 397–411.

[9]

Z. M. Younossi, M. Stepanova, Y. Younossi, et al., “Epidemiology of Chronic Liver Diseases in the USA in the Past Three Decades,” Gut 69, no. 3 (2020): 564–568.

[10]

F. Nassir, “NAFLD: Mechanisms, Treatments, and Biomarkers,” Biomolecules 12, no. 6 (2022): 824.

[11]

G. R. Steinberg, C. M. Valvano, W. De Nardo, and M. J. Watt, “Integrative Metabolism in MASLD and MASH: Pathophysiology and Emerging Mechanisms,” Journal of Hepatology 83, no. 2 (2025): 584–595.

[12]

M. Zhang, J. Ji, J. Song, et al., “Current Therapeutic Targets for Alcohol-Associated Liver Disease,” The American Journal of Pathology 196, no. 1 (2025): 121–135.

[13]

X. Tan, Y. Xiang, J. Shi, L. Chen, and D. Yu, “Targeting NTCP for Liver Disease Treatment: A Promising Strategy,” Journal of Pharmaceutical Analysis 14, no. 9 (2024): 100979.

[14]

W. Deng, F. Chen, Y. Zhao, M. Zhou, and M. Guo, “Anti-hepatitis B Virus Activities of Natural Products and Their Antiviral Mechanisms,” Chinese Journal of Natural Medicines 21, no. 11 (2023): 803–811.

[15]

J. Mondal, P. Samui, A. N. Chatterjee, and B. Ahmad, “Modeling Hepatocyte Apoptosis in Chronic HCV Infection With Impulsive Drug Control,” Applied Mathematical Modelling 136 (2024): 115625.

[16]

H. You, X. Wang, L. Ma, et al., “Insights Into the Impact of hepatitis B Virus on Hepatic Stellate Cell Activation,” Cell Communication and Signaling 21, no. 1 (2023): 70.

[17]

T. H. Karlsen, T. Folseraas, D. Thorburn, and M. Vesterhus, “Primary Sclerosing Cholangitis—a Comprehensive Review,” Journal of Hepatology 67, no. 6 (2017): 1298–1323.

[18]

H. Wu, C. Chen, S. Ziani, et al., “Fibrotic Events in the Progression of Cholestatic Liver Disease,” Cells 10, no. 5 (2021): 1107.

[19]

Y. Hu, X. Bao, Z. Zhang, et al., “Hepatic Progenitor Cell-originated Ductular Reaction Facilitates Liver Fibrosis Through Activation of Hedgehog Signaling,” Theranostics 14, no. 6 (2024): 2379–2395.

[20]

J.-L. Lu, C.-X. Yu, and L.-J. Song, “Programmed Cell Death in Hepatic Fibrosis: Current and Perspectives,” Cell Death Discovery 9, no. 1 (2023): 449.

[21]

Y. Li, J. Wu, R. Liu, Y. Zhang, and X. Li, “Extracellular Vesicles: Catching the Light of Intercellular Communication in Fibrotic Liver Diseases,” Theranostics 12, no. 16 (2022): 6955–6971.

[22]

M. Zhang, E. Xia, C. Li, et al., “The Heterogeneity of Monocyte-derived Macrophages in MASH Pathogenesis,” Cell Communication and Signaling 24, no. 1 (2025): 5.

[23]

P. Horn and F. Tacke, “Metabolic Reprogramming in Liver Fibrosis,” Cell Metabolism 36, no. 7 (2024): 1439–1455.

[24]

H. Akkız, R. K. Gieseler, and A. Canbay, “Liver Fibrosis: From Basic Science Towards Clinical Progress, Focusing on the Central Role of Hepatic Stellate Cells,” International Journal of Molecular Sciences 25, no. 14 (2024): 7873.

[25]

I. Mannaerts, S. B. Leite, S. Verhulst, et al., “The Hippo Pathway Effector YAP Controls Mouse Hepatic Stellate Cell Activation,” Journal of Hepatology 63, no. 3 (2015): 679–688.

[26]

M. J. Binder, S. McCoombe, E. D. Williams, D. R. McCulloch, and A. C. Ward, “The Extracellular Matrix in Cancer Progression: Role of Hyalectan Proteoglycans and ADAMTS Enzymes,” Cancer Letters 385 (2017): 55–64.

[27]

S. Sharma, V. Prathigudupu, C. Cable, et al., “Resolving Fibrosis by Stimulating HSC-dependent Extracellular Matrix Degradation,” Science Translational Medicine 17, no. 813 (2025): eads9470.

[28]

M. A. Karsdal, S. H. Nielsen, D. J. Leeming, et al., “The Good and the Bad Collagens of Fibrosis – Their Role in Signaling and Organ Function,” Advanced Drug Delivery Reviews 121 (2017): 43–56.

[29]

E. J. Lawitz, D. E. Shevell, G. S. Tirucherai, et al., “BMS-986263 in Patients With Advanced Hepatic Fibrosis: 36-week Results From a Randomized, Placebo-controlled Phase 2 Trial,” Hepatology (Baltimore, Md) 75, no. 4 (2022): 912–923.

[30]

S. A. Harrison, M. F. Abdelmalek, S. Caldwell, et al., “Simtuzumab Is Ineffective for Patients With Bridging Fibrosis or Compensated Cirrhosis Caused by Nonalcoholic Steatohepatitis,” Gastroenterology 155, no. 4 (2018): 1140–1153.

[31]

J. Gleeson, J. Barry, and S. O'Reilly, “Use of Liver Imaging and Biopsy in Clinical Practice,” The New England Journal of Medicine 377, no. 23 (2017): 2296.

[32]

P. Bedossa, “Utility and Appropriateness of the Fatty Liver Inhibition of Progression (FLIP) Algorithm and Steatosis, Activity, and Fibrosis (SAF) Score in the Evaluation of Biopsies of Nonalcoholic Fatty Liver Disease,” Hepatology (Baltimore, Md) 60, no. 2 (2014): 565–575.

[33]

S. G. Hübscher, “Histological Grading and Staging in Chronic hepatitis: Clinical Applications and Problems,” Journal of Hepatology 29, no. 6 (1998): 1015–1022.

[34]

Intraobserver and Interobserver Variations in Liver Biopsy Interpretation in Patients With Chronic hepatitis C. The French METAVIR Cooperative Study Group. Hepatology (Baltimore, Md) 1994; 20(1): 15–20.

[35]

Y. E. Chon, Y. J. Jin, and J. An, “Optimal Cut-offs of Vibration-controlled Transient Elastography and Magnetic Resonance Elastography in Diagnosing Advanced Liver Fibrosis in Patients With Nonalcoholic Fatty Liver Disease: A Systematic Review and Meta-analysis,” Clinical and Molecular Hepatology 30, no. Suppl (2024): S117–S133.

[36]

T. Kakegawa, K. Sugimoto, H. Kuroda, Y. Suzuki, K. Imajo, and H. Toyoda, “Diagnostic Accuracy of Two-Dimensional Shear Wave Elastography for Liver Fibrosis: A Multicenter Prospective Study,” Clinical Gastroenterology and Hepatology: The Official Clinical Practice Journal of the American Gastroenterological Association 20, no. 6 (2022): e1478–e1482.

[37]

L. Castera, M. E. Rinella, and E. A. Tsochatzis, “Noninvasive Assessment of Liver Fibrosis,” The New England Journal of Medicine 393, no. 17 (2025): 1715–1729.

[38]

Y. Honda, M. Yoneda, T. Kobayashi, et al., “Meta-analysis of the Diagnostic Accuracy of Serum Type IV Collagen 7S Concentration for the Staging of Liver Fibrosis in Nonalcoholic Fatty Liver Disease,” Hepatology Research: The Official Journal of the Japan Society of Hepatology 53, no. 3 (2023): 219–227.

[39]

K. Kozumi, T. Kodama, H. Murai, et al., “Transcriptomics Identify Thrombospondin-2 as a Biomarker for NASH and Advanced Liver Fibrosis,” Hepatology (Baltimore, Md) 74, no. 5 (2021): 2452–2466.

[40]

W. Li, Y. Chi, and X. Xiao, “Plasma FSTL-1 as a Noninvasive Diagnostic Biomarker for Patients With Advanced Liver Fibrosis,” Hepatology (Baltimore, Md) 82, no. 3 (2025): 669–682.

[41]

L. J. Tang, H. L. Ma, M. Eslam, et al., “Among Simple Non-invasive Scores, Pro-C3 and ADAPT Best Exclude Advanced Fibrosis in Asian Patients With MAFLD,” Metabolism: Clinical and Experimental 128 (2022): 154958.

[42]

A. Nakajima, Y. Eguchi, M. Yoneda, et al., “Randomised Clinical Trial: Pemafibrate, a Novel Selective Peroxisome Proliferator-activated Receptor Alpha Modulator (SPPARMalpha), Versus Placebo in Patients With Non-alcoholic Fatty Liver Disease,” Alimentary Pharmacology & Therapeutics 54, no. 10 (2021): 1263–1277.

[43]

F. Bril, S. Kalavalapalli, V. C. Clark, et al., “Response to Pioglitazone in Patients With Nonalcoholic Steatohepatitis With vs Without Type 2 Diabetes,” Clinical Gastroenterology and Hepatology 16, no. 4 (2018): 558–566.e2.

[44]

S. A. Harrison, C. Thang, S. Bolze, et al., “Evaluation of PXL065 - deuterium-stabilized (R)-pioglitazone in Patients With NASH: A Phase II Randomized Placebo-controlled Trial (DESTINY-1),” Journal of Hepatology 78, no. 5 (2023): 914–925.

[45]

S. A. Harrison, N. Alkhouri, B. A. Davison, et al., “Insulin Sensitizer MSDC-0602K in Non-alcoholic Steatohepatitis: A Rand Omized, Double-blind, Placebo-controlled Phase IIb Study,” Journal of Hepatology 72, no. 4 (2020): 613–626.

[46]

S. Lefere, T. Puengel, J. Hundertmark, et al., “Differential Effects of Selective- and Pan-PPAR Agonists on Experimental Steatohepatitis and Hepatic Macrophages(☆),” Journal of Hepatology 73, no. 4 (2020): 757–770.

[47]

N. Venkateswaran, “Seladelpar as an Alternate Second-Line Agent for Primary Biliary Cirrhosis,” Gastroenterology 167, no. 5 (2024): 1047.

[48]

M. R. Jain, S. R. Giri, B. Bhoi, et al., “Dual PPARalpha/Gamma Agonist Saroglitazar Improves Liver Histopathology and Biochemistry in Experimental NASH Models,” Liver International 38, no. 6 (2018): 1084–1094.

[49]

S. Gawrieh, M. Noureddin, N. Loo, et al., “Saroglitazar, a PPAR-alpha/Gamma Agonist, for Treatment of NAFLD: A Randomized Controlled Double-Blind Phase 2 Trial,” Hepatology 74, no. 4 (2021): 1809–1824.

[50]

V. Ratziu, S. A. Harrison, S. Francque, et al., “Elafibranor, an Agonist of the Peroxisome Proliferator-Activated Receptor-alpha and -delta, Induces Resolution of Nonalcoholic Steatohepatitis Without Fibrosis Worsening,” Gastroenterology 150, no. 5 (2016): 1147–1159 e5.

[51]

Z. Boyer-Diaz, P. Aristu-Zabalza, M. Andres-Rozas, et al., “Pan-PPAR Agonist Lanifibranor Improves Portal Hypertension and Hepatic Fibrosis in Experimental Advanced Chronic Liver Disease,” Journal of Hepatology 74, no. 5 (2021): 1188–1199.

[52]

S. M. Francque, P. Bedossa, V. Ratziu, et al., “A Randomized, Controlled Trial of the Pan-PPAR Agonist Lanifibranor in NASH,” New England Journal of Medicine 385, no. 17 (2021): 1547–1558.

[53]

R. Loomba, A. J. Sanyal, A. Nakajima, et al., “Pegbelfermin in Patients with Nonalcoholic Steatohepatitis and Stage 3 Fibrosis (FALCON 1): A Randomized Phase 2b Study,” Clinical Gastroenterology and Hepatology 22, no. 1 (2024): 102–112.

[54]

S. A. Harrison, P. J. Ruane, B. L. Freilich, et al., “Efruxifermin in Non-alcoholic Steatohepatitis: A Randomized, Double-blind, Placebo-controlled, Phase 2a Trial,” Nature Medicine 27, no. 7 (2021): 1262–1271.

[55]

R. Loomba, K. V. Kowdley, J. Rodriguez, et al., “Efimosfermin Alfa (BOS-580), a Long-acting FGF21 Analogue, in Participants With Phenotypic Metabolic Dysfunction-associated Steatohepatitis: A Multicentre, Randomised, Double-blind, Placebo-controlled, Phase 2a Trial,” The Lancet Gastroenterology & Hepatology 10, no. 8 (2025): 734–745.

[56]

M. Noureddin, J. P. Frias, G. W. Neff, et al., “Safety and Efficacy of Once-weekly Efruxifermin Versus Placebo in Metabolic Dysfunction-associated Steatohepatitis (HARMONY): 96-week Results From a Multicentre, Randomised, Double-blind, Placebo-controlled, Phase 2b Trial,” Lancet (London, England) 406, no. 10504 (2025): 719–730.

[57]

M. Noureddin, M. E. Rinella, N. P. Chalasani, et al., “Efruxifermin in Compensated Liver Cirrhosis Caused by MASH,” The New England Journal of Medicine 392, no. 24 (2025): 2413–2424.

[58]

R. A. Sinha, B. K. Singh, and P. M. Yen, “Direct Effects of Thyroid Hormones on Hepatic Lipid Metabolism,” Nature Reviews Endocrinology 14, no. 5 (2018): 259–269.

[59]

A. Kannt, P. Wohlfart, A. N. Madsen, S. S. Veidal, M. Feigh, and D. Schmoll, “Activation of Thyroid Hormone Receptor-beta Improved Disease Activity and Metabolism Independent of Body Weight in a Mouse Model of Non-alcoholic Steatohepatitis and Fibrosis,” British Journal of Pharmacology 178, no. 12 (2021): 2412–2423.

[60]

X. Wang, L. Wang, L. Geng, N. Tanaka, and B. Ye, “Resmetirom Ameliorates NASH-Model Mice by Suppressing STAT3 and NF-kappaB Signaling Pathways in an RGS5-Dependent Manner,” International Journal of Molecular Sciences 24, no. 6 (2023): 5843.

[61]

Z. M. Younossi, M. Stepanova, R. A. Taub, J. M. Barbone, and S. A. Harrison, “Hepatic Fat Reduction due to Resmetirom in Patients with Nonalcoholic Steatohepatitis Is Associated with Improvement of Quality of Life,” Clinical Gastroenterology and Hepatology 20, no. 6 (2022): 1354–1361 e7.

[62]

S. A. Harrison, M. R. Bashir, C. D. Guy, et al., “Resmetirom (MGL-3196) for the Treatment of Non-alcoholic Steatohepatit Is: A Multicentre, Randomised, Double-blind, Placebo-controlled, Phase 2 Trial,” Lancet (London, England) 394, no. 10213 (2019): 2012–2024.

[63]

J. Zhou, L. R. Waskowicz, A. Lim, et al., “A Liver-Specific Thyromimetic, VK2809, Decreases Hepatosteatosis in Glycogen Storage Disease Type Ia,” Thyroid: Official Journal of the American Thyroid Association 29, no. 8 (2019): 1158–1167.

[64]

R. Loomba, R. Mohseni, K. J. Lucas, et al., “TVB-2640 (FASN Inhibitor) for the Treatment of Nonalcoholic Steatohepatitis: FASCINATE-1, a Randomized, Placebo-Controlled Phase 2a Trial,” Gastroenterology 161, no. 5 (2021): 1475–1486.

[65]

E. J. Lawitz, A. Coste, F. Poordad, et al., “Acetyl-CoA Carboxylase Inhibitor GS-0976 for 12 Weeks Reduces Hepatic De Novo Lipogenesis and Steatosis in Patients with Nonalcoholic Steato hepatitis,” Clinical Gastroenterology and Hepatology 16, no. 12 (2018): 1983–1991.e3.

[66]

R. Loomba, Z. Kayali, M. Noureddin, et al., “GS-0976 Reduces Hepatic Steatosis and Fibrosis Markers in Patients with Nonalcoholic Fatty Liver Disease,” Gastroenterology 155, no. 5 (2018): 1463–1473.e6.

[67]

R. Loomba, M. Noureddin, K. V. Kowdley, et al., “Combination Therapies Including Cilofexor and Firsocostat for Bridging Fibrosis and Cirrhosis Attributable to NASH,” Hepatology (Baltimore, Md) 73, no. 2 (2021): 625–643.

[68]

M. E. Rinella, J. F. Trotter, M. F. Abdelmalek, et al., “Rosuvastatin Improves the FGF19 Analogue NGM282-associated Lipid Changes in Patients With Non-alcoholic Steatohepatitis,” Journal of Hepatology 70, no. 4 (2019): 735–744.

[69]

Y. Cho, H. Rhee, Y. E. Kim, et al., “Ezetimibe Combination Therapy With statin for Non-alcoholic Fatty Liver Disease: An Open-label Randomized Controlled Trial (ESSENTIAL study),” BMC Medicine 20, no. 1 (2022): 93.

[70]

R. A. Calle, N. B. Amin, S. Carvajal-Gonzalez, et al., “ACC Inhibitor Alone or co-administered With a DGAT2 Inhibitor in Patie Nts With Non-alcoholic Fatty Liver Disease: Two Parallel, Placebo-Controlled, Randomized Phase 2a Trials,” Nature Medicine 27, no. 10 (2021): 1836–1848.

[71]

Y. S. Gao, M. Y. Qian, Q. Q. Wei, et al., “WZ66, a Novel Acetyl-CoA Carboxylase Inhibitor, Alleviates Nonalcoholic Steatohepatitis (NASH) in Mice,” Acta Pharmacologica Sinica 41, no. 3 (2020): 336–347.

[72]

V. Ratziu, L. de Guevara, R. Safadi, et al., “Aramchol in Patients With Nonalcoholic Steatohepatitis: A Randomized, Double-blind, Placebo-controlled Phase 2b Trial,” Nature Medicine 27, no. 10 (2021): 1825–1835.

[73]

N. B. Amin, S. Carvajal-Gonzalez, J. Purkal, et al., “Targeting Diacylglycerol Acyltransferase 2 for the Treatment of Nonalc Oholic Steatohepatitis,” Science Translational Medicine 11, no. 520 (2019): eaav9701.

[74]

E. Nozari, A. Moradi, and M. Samadi, “Effect of Atorvastatin, Curcumin, and Quercetin on miR-21 and miR-122 and Their Correlation With TGFbeta1 Expression in Experimental Liver Fibrosis,” Life Sciences 259 (2020): 118293.

[75]

M. L. Hartman, A. J. Sanyal, R. Loomba, et al., “Effects of Novel Dual GIP and GLP-1 Receptor Agonist Tirzepatide on Biomarkers of Nonalcoholic Steatohepatitis in Patients with Type 2 Diabetes,” Diabetes Care 43, no. 6 (2020): 1352–1355.

[76]

P. N. Newsome, A. J. Sanyal, K. A. Engebretsen, et al., “Semaglutide 2.4 mg in Participants with Metabolic Dysfunction-Associated Steatohepatitis: Baseline Characteristics and Design of the Phase 3 ESSENCE Trial,” Alimentary Pharmacology & Therapeutics 60, no. 11-12 (2024): 1525–1533.

[77]

M. J. Armstrong, P. Gaunt, G. P. Aithal, et al., “Liraglutide Safety and Efficacy in Patients With Non-alcoholic Steatohepatitis (LEAN): A Multicentre, Double-blind, Randomised, Placebo-controlled Phase 2 Study,” Lancet 387, no. 10019 (2016): 679–690.

[78]

E. M. Desjardins, J. Wu, D. C. T. Lavoie, et al., “Combination of an ACLY Inhibitor With a GLP-1R Agonist Exerts Additive Benefits on Nonalcoholic Steatohepatitis and Hepatic Fibrosis in Mice,” Cell Reports Medicine 4, no. 9 (2023): 101193.

[79]

N. Perakakis, K. Stefanakis, M. Feigh, S. S. Veidal, and C. S. Mantzoros, “Elafibranor and Liraglutide Improve Differentially Liver Health and Metabolism in a Mouse Model of Non-alcoholic Steatohepatitis,” Liver International 41, no. 8 (2021): 1853–1866.

[80]

P. N. Newsome, K. Buchholtz, K. Cusi, et al., “A Placebo-Controlled Trial of Subcutaneous Semaglutide in Nonalcoholic Steatohepatitis,” New England Journal of Medicine 384, no. 12 (2021): 1113–1124.

[81]

R. Loomba, M. F. Abdelmalek, M. J. Armstrong, et al., “Semaglutide 2.4 mg Once Weekly in Patients With Non-alcoholic Steatohepatitis-related Cirrhosis: A Randomised, Placebo-controlled Phase 2 Trial,” The Lancet Gastroenterology & Hepatology 8, no. 6 (2023): 511–522.

[82]

N. Alkhouri, R. Herring, H. Kabler, et al., “Safety and Efficacy of Combination Therapy With Semaglutide, Cilofexor and Firsocostat in Patients With Non-alcoholic Steatohepatitis: A Randomised, Open-label Phase II Trial,” Journal of Hepatology 77, no. 3 (2022): 607–618.

[83]

M. L. Boland, R. C. Laker, K. Mather, et al., “Resolution of NASH and Hepatic Fibrosis by the GLP-1R/GcgR Dual-agonist Cotadutide via Modulating Mitochondrial Function and Lipogenesis,” Nature Metabolism 2, no. 5 (2020): 413–431.

[84]

M. Noureddin, S. A. Harrison, R. Loomba, et al., “Safety and Efficacy of Weekly Pemvidutide versus Placebo for Metabolic Dysfunction-associated Steatohepatitis (IMPACT): 24-week Results From a Multicentre, Randomised, Double-blind, Phase 2b Study,” Lancet (London, England) 406, no. 10520 (2025): 2644–2655.

[85]

J. Lin, Y. Huang, B. Xu, et al., “Effect of dapagliflozin on Metabolic Dysfunction-associated Steatohepatitis: Multicentre, Double Blind, Randomised, Placebo Controlled Trial,” BMJ (Clinical Research Ed) 389 (2025): e083735.

[86]

A. Gastaldelli, E. Repetto, C. Guja, et al., “Exenatide and Dapagliflozin Combination Improves Markers of Liver Steatosis and Fibrosis in Patients With Type 2 Diabetes,” Diabetes, Obesity and Metabolism 22, no. 3 (2020): 393–403.

[87]

Y. Shen, L. Cheng, M. Xu, et al., “SGLT2 inhibitor Empagliflozin Downregulates miRNA-34a-5p and Targets G REM2 to Inactivate Hepatic Stellate Cells and Ameliorate Non-alcoholic Fatty Liver Disease-associated Fibrosis,” Metabolism 146 (2023): 155657.

[88]

K. Fan, K. Wu, L. Lin, et al., “Metformin Mitigates Carbon Tetrachloride-induced TGF-β1/Smad3 Signalin g and Liver Fibrosis in Mice,” Biomedicine & Pharmacotherapy 90 (2017): 421–426.

[89]

A. M. Abdelhamid, M. E. Youssef, E. E. Abd El-Fattah, et al., “Blunting p38 MAPKα and ERK1/2 Activities by empagliflozin Enhances the Antifibrotic Effect of Metformin and Augments Its AMPK-induced NF-κB Inactivation in Mice Intoxicated With Carbon Tetrachloride,” Life Sciences 286 (2021): 120070.

[90]

R. C. Shankaraiah, E. Callegari, P. Guerriero, et al., “Metformin Prevents Liver Tumourigenesis by Attenuating Fibrosis in a Transgenic Mouse Model of Hepatocellular Carcinoma,” Oncogene 38, no. 45 (2019): 7035–7045.

[91]

E. Vilar-Gomez, R. Vuppalanchi, A. P. Desai, et al., “Long-term Metformin Use May Improve Clinical Outcomes in Diabetic Patients With Non-alcoholic Steatohepatitis and Bridging Fibrosis or Compensated Cirrhosis,” Alimentary Pharmacology & Therapeutics 50, no. 3 (2019): 317–328.

[92]

M. Shimizu, K. Suzuki, K. Kato, et al., “Evaluation of the Effects of dapagliflozin, a Sodium-glucose co-transporter-2 Inhibitor, on Hepatic Steatosis and Fibrosis Using Transient Elastography in Patients With Type 2 Diabetes and Non-alcoholic Fatty Liver Disease,” Diabetes, Obesity and Metabolism 21, no. 2 (2019): 285–292.

[93]

K. Cusi, N. Alkhouri, S. A. Harrison, et al., “Efficacy and Safety of PXL770, a Direct AMP Kinase Activator, for the Treatment of Non-alcoholic Fatty Liver Disease (STAMP-NAFLD): A Randomised, Double-blind, Placebo-controlled, Phase 2a Study,” The Lancet Gastroenterology & Hepatology 6, no. 11 (2021): 889–902.

[94]

L. Adorini and M. Trauner, “FXR Agonists in NASH Treatment,” Journal of Hepatology 79, no. 5 (2023): 1317–1331.

[95]

K. D. Lindor, C. L. Bowlus, J. Boyer, C. Levy, and M. Mayo, “Primary Biliary Cholangitis: 2018 Practice Guidance From the American Association for the Study of Liver Diseases,” Hepatology 69, no. 1 (2019): 394–419.

[96]

G. M. Hirschfield, U. Beuers, C. Corpechot, et al., “EASL Clinical Practice Guidelines: The Diagnosis and Management of Patients With Primary Biliary Cholangitis,” Journal of Hepatology 67, no. 1 (2017): 145–172.

[97]

K. V. Kowdley, R. Vuppalanchi, C. Levy, et al., “A Randomized, Placebo-controlled, Phase II Study of Obeticholic Acid for Primary Sclerosing Cholangitis,” Journal of Hepatology 73, no. 1 (2020): 94–101.

[98]

Z. M. Younossi, V. Ratziu, R. Loomba, et al., “Obeticholic Acid for the Treatment of Non-alcoholic Steatohepatitis: Interim Analysis From a Multicentre, Randomised, Placebo-controlled Phase 3 Trial,” Lancet 394, no. 10215 (2019): 2184–2196.

[99]

J. Zhou, N. Huang, Y. Guo, et al., “Combined Obeticholic Acid and Apoptosis Inhibitor Treatment Alleviates Liver Fibrosis,” APSB 9, no. 3 (2019): 526–536.

[100]

P. An, G. Wei, P. Huang, et al., “A Novel Non-bile Acid FXR Agonist EDP-305 Potently Suppresses Liver Injury and Fibrosis Without Worsening of Ductular Reaction,” Liver International 40, no. 7 (2020): 1655–1669.

[101]

V. Ratziu, M. E. Rinella, B. A. Neuschwander-Tetri, et al., “EDP-305 in Patients With NASH: A Phase II Double-blind Placebo-control Led Dose-ranging Study,” Journal of Hepatology 76, no. 3 (2022): 506–517.

[102]

M. Trauner, A. Gulamhusein, B. Hameed, et al., “The Nonsteroidal Farnesoid X Receptor Agonist Cilofexor (GS-9674) Improves Markers of Cholestasis and Liver Injury in Patients with Primary Sclerosing Cholangitis,” Hepatology 70, no. 3 (2019): 788–801.

[103]

K. Patel, S. A. Harrison, M. Elkhashab, et al., “Cilofexor, a Nonsteroidal FXR Agonist, in Patients with Noncirrhotic N ASH: A Phase 2 Randomized Controlled Trial,” Hepatology (Baltimore, Md) 72, no. 1 (2020): 58–71.

[104]

M. Trauner, C. Levy, A. Tanaka, et al., “Cilofexor in Non-cirrhotic Primary Sclerosing Cholangitis (PRIMIS): A Randomised, Double-blind, Multicentre, Placebo-controlled, Phase 3 Trial,” The Lancet Gastroenterology & Hepatology 11, no. 1 (2026): 46–58.

[105]

D. C. Tully, P. V. Rucker, D. Chianelli, et al., “Discovery of Tropifexor (LJN452), a Highly Potent Non-bile Acid FXR Agonist for the Treatment of Cholestatic Liver Diseases and Nonalcoholic Steatohepatitis (NASH),” Journal of Medicinal Chemistry 60, no. 24 (2017): 9960–9973.

[106]

Q. M. Anstee, K. J. Lucas, S. Francque, et al., “Tropifexor plus cenicriviroc Combination versus Monotherapy in Nonalcoholic Steatohepatitis: Results From the Phase 2b TANDEM Study,” Hepatology 78, no. 4 (2023): 1223–1239.

[107]

V. Ratziu, S. A. Harrison, V. Loustaud-Ratti, et al., “Hepatic and Renal Improvements With FXR Agonist vonafexor in Individuals With Suspected Fibrotic NASH,” Journal of Hepatology 78, no. 3 (2023): 479–492.

[108]

R. Erken, P. Andre, E. Roy, et al., “Farnesoid X Receptor Agonist for the Treatment of Chronic hepatitis B: A Safety Study,” Journal of Viral Hepatitis 28, no. 12 (2021): 1690–1698.

[109]

S. A. Harrison, M. R. Bashir, K. J. Lee, et al., “A Structurally Optimized FXR Agonist, MET409, Reduced Liver Fat Content Over 12 Weeks in Patients With Non-alcoholic Steatohepatitis,” Journal of Hepatology 75, no. 1 (2021): 25–33.

[110]

S. Fiorucci, M. Biagioli, V. Sepe, A. Zampella, and E. Distrutti, “Bile Acid Modulators for the Treatment of Nonalcoholic Steatohepatitis (NASH),” Expert Opinion on Investigational Drugs 29, no. 6 (2020): 623–632.

[111]

J. Yang, T. Zhao, J. Fan, et al., “Structure-guided Discovery of Bile Acid Derivatives for Treating Liver Diseases Without Causing Itch,” Cell 187, no. 25 (2024): 7164–7182.

[112]

M. Wagner and P. Fickert, “Drug Therapies for Chronic Cholestatic Liver Diseases,” Annual Review of Pharmacology and Toxicology 60 (2020): 503–527.

[113]

M. Mueller, A. Thorell, T. Claudel, et al., “Ursodeoxycholic Acid Exerts Farnesoid X Receptor-antagonistic Effects on Bile Acid and Lipid Metabolism in Morbid Obesity,” Journal of Hepatology 62, no. 6 (2015): 1398–1404.

[114]

H. L. Ye, J. W. Zhang, X. Z. Chen, P. B. Wu, L. Chen, and G. Zhang, “Ursodeoxycholic Acid Alleviates Experimental Liver Fibrosis Involving Inhibition of Autophagy,” Life Sciences 242 (2020): 117175.

[115]

S. A. Harrison, S. J. Rossi, A. H. Paredes, et al., “NGM282 Improves Liver Fibrosis and Histology in 12 Weeks in Patients with Nonalcoholic Steatohepatitis,” Hepatology 71, no. 4 (2020): 1198–1212.

[116]

S. A. Harrison, M. F. Abdelmalek, G. Neff, et al., “Aldafermin in Patients With Non-alcoholic Steatohepatitis (ALPINE 2/3): A Randomised, Double-blind, Placebo-controlled, Phase 2b Trial,” The Lancet Gastroenterology & Hepatology 7, no. 7 (2022): 603–616.

[117]

X. Xue, H. Zhou, J. Gao, et al., “The Impact of Traditional Chinese Medicine and Dietary Compounds on Modulating Gut Microbiota in Hepatic Fibrosis: A Review,” Heliyon 10, no. 19 (2024): e38339.

[118]

G. Rong, Y. Chen, Z. Yu, et al., “Synergistic Effect of Biejia-Ruangan on Fibrosis Regression in Patients with Chronic Hepatitis B Treated with Entecavir: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial,” Journal of Infectious Diseases 225, no. 6 (2022): 1091–1099.

[119]

D. Ji, Y. Chen, J. Bi, et al., “Entecavir plus Biejia-Ruangan Compound Reduces the Risk of Hepatocellu Lar Carcinoma in Chinese Patients With Chronic hepatitis B,” Journal of Hepatology 77, no. 6 (2022): 1515–1524.

[120]

Y. C. Hsu, C. Y. Chen, I. W. Chang, et al., “Once-daily Tenofovir Disoproxil Fumarate in Treatment-naive Taiwanese Patients With Chronic hepatitis B and Minimally Raised Alanine Aminotransferase (TORCH-B): A Multicentre, Double-blind, Placebo-controlled, Parallel-group, Randomised Trial,” The Lancet Infectious Diseases 21, no. 6 (2021): 823–833.

[121]

A. Boyd, J. Bottero, P. Miailhes, et al., “Liver Fibrosis Regression and Progression During Controlled hepatitis B Virus Infection Among HIV-HBV Patients Treated With Tenofovir Disoproxil Fumarate in France: A Prospective Cohort Study,” Journal of the International AIDS Society 20, no. 1 (2017): 21426.

[122]

P. Manousou, E. Cholongitas, D. Samonakis, et al., “Reduced Fibrosis in Recurrent HCV With Tacrolimus, Azathioprine and Steroids versus Tacrolimus: Randomised Trial Long Term Outcomes,” Gut 63, no. 6 (2014): 1005–1013.

[123]

F. G. Villamil, A. C. Gadano, F. Zingale, et al., “Fibrosis Progression in Maintenance Liver Transplant Patients With hepatitis C Recurrence: A Randomised Study of Everolimus vs. calcineurin Inhibitors,” Liver International 34, no. 10 (2014): 1513–1521.

[124]

S. Martini, M. Sacco, S. Strona, et al., “Impact of Viral Eradication With Sofosbuvir-based Therapy on the Outcome of Post-transplant hepatitis C With Severe Fibrosis,” Liver International 37, no. 1 (2017): 62–70.

[125]

A. Bettaieb, J. X. Jiang, Y. Sasaki, et al., “Hepatocyte Nicotinamide Adenine Dinucleotide Phosphate Reduced Oxidase 4 Regulates Stress Signaling, Fibrosis, and Insulin Sensitivity during Development of Steatohepatitis in Mice,” Gastroenterology 149, no. 2 (2015): 468–80 e10.

[126]

P. Invernizzi, M. Carbone, D. Jones, et al., “Setanaxib, a First-in-class Selective NADPH Oxidase 1/4 Inhibitor for Primary Biliary Cholangitis: A Randomized, Placebo-controlled, Phase 2 Trial,” Liver International 43, no. 7 (2023): 1507–1522.

[127]

H. Chen, Q. Gan, C. Yang, et al., “A Novel Role of Glutathione S-transferase A3 in Inhibiting Hepatic Stellate Cell Activation and Rat Hepatic Fibrosis,” Journal of Translational Medicine 17, no. 1 (2019): 280.

[128]

F. E. M. Ali, A. G. Bakr, A. M. Abo-Youssef, A. A. Azouz, and R. A. M. Hemeida, “Targeting Keap-1/Nrf-2 Pathway and Cytoglobin as a Potential Protective Mechanism of Diosmin and Pentoxifylline Against Cholestatic Liver Cirrhosis,” Life Sciences 207 (2018): 50–60.

[129]

A. Zhuge, S. Li, Y. Yuan, et al., “Microbiota-induced Lipid Peroxidation Impairs Obeticholic Acid-mediated Antifibrotic Effect towards Nonalcoholic Steatohepatitis in Mice,” Redox Biology 59 (2023): 102582.

[130]

S. M. El-Haggar and T. M. Mostafa, “Comparative Clinical Study Between the Effect of Fenofibrate Alone and Its Combination With Pentoxifylline on Biochemical Parameters and Liver Stiffness in Patients With Non-alcoholic Fatty Liver Disease,” Hepatology International 9, no. 3 (2015): 471–479.

[131]

Y. Xi, Y. Li, P. Xu, et al., “The Anti-fibrotic Drug Pirfenidone Inhibits Liver Fibrosis by Targeting the Small Oxidoreductase Glutaredoxin-1,” Science Advances 7, no. 36 (2021): eabg9241.

[132]

J. L. Poo, A. Torre, J. R. Aguilar-Ramirez, et al., “Benefits of Prolonged-release Pirfenidone plus Standard of Care Treatment in Patients With Advanced Liver Fibrosis: PROMETEO Study,” Hepatology International 14, no. 5 (2020): 817–827.

[133]

X. Zhong and H. Liu, “Baicalin Attenuates Diet Induced Nonalcoholic Steatohepatitis by Inhibiting Inflammation and Oxidative Stress via Suppressing JNK Signaling Pathways,” Biomedicine & Pharmacotherapy 98 (2018): 111–117.

[134]

G. M. Alshammari, W. H. Al-Qahtani, N. A. AlFaris, N. S. Alzahrani, M. A. Alkhateeb, and M. A. Yahya, “Quercetin Prevents Cadmium Chloride-induced Hepatic Steatosis and Fibrosis by Downregulating the Transcription of miR-21,” Biofactors 47, no. 3 (2021): 489–505.

[135]

H. Zhou, Y. Liu, Y. Su, et al., “Ginsenoside Rg1 Attenuates Lipopolysaccharide-induced Chronic Liver Da Mage by Activating Nrf2 Signaling and Inhibiting Inflammasomes in Hepa Tic Cells,” Journal of Ethnopharmacology 324 (2024): 117794.

[136]

W. J. Liu, W. W. Chen, J. Y. Chen, et al., “Baicalin Attenuated Metabolic Dysfunction-associated Fatty Liver Disease by Suppressing Oxidative Stress and Inflammation via the p62-Keap1-Nrf2 Signalling Pathway in db/db Mice,” Phytotherapy Research 39, no. 4 (2025): 1663–1678.

[137]

Y. J. Choi, D. H. Kim, S. J. Kim, et al., “Decursin Attenuates Hepatic Fibrogenesis Through Interrupting TGF-beta-mediated NAD(P)H Oxidase Activation and Smad Signaling in Vivo and in Vitro,” Life Sciences 108, no. 2 (2014): 94–103.

[138]

R. Li, J. Li, Y. Huang, et al., “Polydatin Attenuates Diet-induced Nonalcoholic Steatohepatitis and Fibrosis in Mice,” International Journal of Molecular Sciences 14, no. 11 (2018): 1411–1425.

[139]

J. Li, R. Hu, S. Xu, et al., “Xiaochaihutang Attenuates Liver Fibrosis by Activation of Nrf2 Pathway in Rats,” Biomedicine & Pharmacotherapy 96 (2017): 847–853.

[140]

R. Loomba, E. Lawitz, P. S. Mantry, et al., “The ASK1 Inhibitor selonsertib in Patients With Nonalcoholic Steatohepatitis: A Randomized, Phase 2 Trial,” Hepatology 67, no. 2 (2018): 549–559.

[141]

S. A. Harrison, V. W. Wong, T. Okanoue, et al., “Selonsertib for Patients With Bridging Fibrosis or Compensated Cirrhosis due to NASH: Results From Randomized Phase III STELLAR Trials,” Journal of Hepatology 73, no. 1 (2020): 26–39.

[142]

C. T. Frenette, G. Morelli, M. L. Shiffman, et al., “Emricasan Improves Liver Function in Patients with Cirrhosis and High Model for End-Stage Liver Disease Scores Compared with Placebo,” Clinical Gastroenterology and Hepatology 17, no. 4 (2019): 774–783.e4.

[143]

S. A. Harrison, Z. Goodman, A. Jabbar, et al., “A Randomized, Placebo-controlled Trial of emricasan in Patients With NASH and F1-F3 Fibrosis,” Journal of Hepatology 72, no. 5 (2020): 816–827.

[144]

N. Sousos, E. Sinakos, P. Klonizakis, et al., “Deferasirox Improves Liver Fibrosis in Beta-thalassaemia Major Patients. A Five-year Longitudinal Study From a Single Thalassaemia Centre,” British Journal of Pharmacology 181, no. 1 (2018): 140–142.

[145]

M. Jiang, C. Huang, Q. Wu, et al., “Sini San Ameliorates CCl4-induced Liver Fibrosis in Mice by Inhibiting AKT-mediated Hepatocyte Apoptosis,” Journal of Ethnopharmacology 303 (2023): 115965.

[146]

X. Chen, X. Sun, S. Ji, H. Yu, and P. Wu, “TMT-based Proteomics Analysis Identifies the Interventional Mechanisms of Qijia Rougan Decoction in Improving Hepatic Fibrosis,” Journal of Ethnopharmacology 319, no. Pt 3 (2024): 117334.

[147]

F.-F. Cai, Y.-Q. Bian, R. Wu, et al., “Yinchenhao Decoction Suppresses Rat Liver Fibrosis Involved in an Apop Tosis Regulation Mechanism Based on Network Pharmacology and Transcrip Tomic Analysis,” Biomedicine & Pharmacotherapy 114 (2019): 108863.

[148]

H. Tian, L. Liu, Z. Li, et al., “Chinese Medicine CGA Formula Ameliorates Liver Fibrosis Induced by Carbon Tetrachloride Involving Inhibition of Hepatic Apoptosis in Rats,” Journal of Ethnopharmacology 232 (2019): 227–235.

[149]

S. L. Friedman, V. Ratziu, S. A. Harrison, et al., “A Randomized, Placebo-controlled Trial of cenicriviroc for Treatment of Nonalcoholic Steatohepatitis With Fibrosis,” Hepatology 67, no. 5 (2018): 1754–1767.

[150]

V. Ratziu, A. Sanyal, S. A. Harrison, et al., “Cenicriviroc Treatment for Adults with Nonalcoholic Steatohepatitis and Fibrosis: Final Analysis of the Phase 2b CENTAUR Study,” Hepatology 72, no. 3 (2020): 892–905.

[151]

Y. Guo, C. Zhao, W. Dai, et al., “C-C Motif Chemokine Receptor 2 Inhibition Reduces Liver Fibrosis by Restoring the Immune Cell Landscape,” International Journal of Biological Sciences 19, no. 8 (2023): 2572–2587.

[152]

Q. M. Anstee, B. A. Neuschwander-Tetri, V. Wai-Sun Wong, et al., “Cenicriviroc Lacked Efficacy to Treat Liver Fibrosis in Nonalcoholic Steatohepatitis: AURORA Phase III Randomized Study,” Clinical Gastroenterology and Hepatology 22, no. 1 (2024): 124–134 e1.

[153]

M. Israelsen, B. S. Madsen, N. Torp, et al., “Rifaximin-alpha for Liver Fibrosis in Patients With Alcohol-related Liver Disease (GALA-RIF): A Randomised, Double-blind, Placebo-controlled, Phase 2 Trial,” The Lancet Gastroenterology & Hepatology 8, no. 6 (2023): 523–532.

[154]

H. Miao, H. Ouyang, Q. Guo, et al., “Chlorogenic Acid Alleviated Liver Fibrosis in Methionine and Choline D Eficient Diet-induced Nonalcoholic Steatohepatitis in Mice and Its mec Hanism,” Journal of Nutritional Biochemistry 106 (2022): 109020.

[155]

X. Sun, Y. Zheng, Y. Tian, et al., “Astragalus Polysaccharide Alleviates Alcoholic-induced Hepatic Fibrosis by Inhibiting Polymerase I and Transcript Release Factor and the TLR 4/JNK/NF-κB/MyD88 Pathway,” Journal of Ethnopharmacology 314 (2023): 116662.

[156]

F. Cao, Y. Zhang, W. Li, K. Shimizu, H. Xie, and C. Zhang, “Mogroside IVE Attenuates Experimental Liver Fibrosis in Mice and Inhibits HSC Activation Through Downregulating TLR4-mediated Pathways,” International Immunopharmacology 55 (2018): 183–192.

[157]

H. W. Zhao, Z. F. Zhang, X. Chai, et al., “Oxymatrine Attenuates CCl4-induced Hepatic Fibrosis via Modulation of TLR4-dependent Inflammatory and TGF-beta1 Signaling Pathways,” International Immunopharmacology 36 (2016): 249–255.

[158]

C. Lee, J. Bak, S. Yoon, and J. O. Moon, “Protective Effect of Oligonol on Dimethylnitrosamine-Induced Liver Fibrosis in Rats via the JNK/NF-kappaB and PI3K/Akt/Nrf2 Signaling Pathways,” Antioxidants (Basel) 10, no. 3 (2021): 1–14.

[159]

X. Lin, Y. Wei, Y. Li, et al., “Tormentic Acid Ameliorates Hepatic Fibrosis in Vivo by Inhibiting Glycerophospholipids Metabolism and PI3K/Akt/mTOR and NF-kappaB Pathways: Based on Transcriptomics and Metabolomics,” Frontiers in Pharmacology 13 (2022): 801982.

[160]

D. K. Mostafa, M. M. Eissa, D. A. Ghareeb, S. Abdulmalek, and W. A. Hewedy, “Resveratrol Protects Against Schistosoma mansoni-induced Liver Fibrosis by Targeting the Sirt-1/NF-kappaB Axis,” Inflammopharmacology 32, no. 1 (2024): 763–775.

[161]

B. de Souza Basso, G. V. Haute, M. Ortega-Ribera, et al., “Methoxyeugenol Deactivates Hepatic Stellate Cells and Attenuates Liver Fibrosis and Inflammation Through a PPAR-ɣ and NF-kB Mechanism,” Journal of Ethnopharmacology 280 (2021): 114433.

[162]

G. Yang, J. H. Jang, S. W. Kim, et al., “Sweroside Prevents Non-Alcoholic Steatohepatitis by Suppressing Activation of the NLRP3 Inflammasome,” International Journal of Molecular Sciences 21, no. 8 (2020): 2790.

[163]

H.-Q. Wang, Z. Wan, Q. Zhang, et al., “Schisandrin B Targets Cannabinoid 2 Receptor in Kupffer Cell to Ameliorate CCl4-induced Liver Fibrosis by Suppressing NF-κB and p38 MAPK Pathway,” Phytomedicine 98 (2022): 153960.

[164]

J. Zhu, R. Wang, T. Xu, et al., “Salvianolic Acid A Attenuates Endoplasmic Reticulum Stress and Protects against Cholestasis-Induced Liver Fibrosis via the SIRT1/HSF1 Pathway,” Frontiers in Pharmacology 9 (2018): 1277.

[165]

R. Cao, C. Cao, X. Hu, et al., “Kaempferol Attenuates Carbon Tetrachloride (CCl4)-induced Hepatic Fibrosis by Promoting ASIC1a Degradation and Suppression of the ASIC1a-mediated ERS,” Phytomedicine 121 (2023): 155125.

[166]

W.-K. Li, G.-F. Wang, T.-M. Wang, et al., “Protective Effect of Herbal Medicine Huangqi Decoction Against Chronic Cholestatic Liver Injury by Inhibiting Bile Acid-stimulated Inflammat Ion in DDC-induced Mice,” Phytomedicine 62 (2019): 152948.

[167]

H. Cao, S. Li, R. Xie, et al., “Exploring the Mechanism of Dangguiliuhuang Decoction against Hepatic Fibrosis by Network Pharmacology and Experimental Validation,” Frontiers in Pharmacology 9 (2018): 187.

[168]

S. Wang, F. Ye, Q. Ren, et al., “The Anti-liver Fibrosis Effect of Tibetan Medicine (Qiwei Tiexie capsu le) Is Related to the Inhibition of NLRP3 Inflammasome Activation in v Ivo and in Vitro,” Journal of Ethnopharmacology 319, no. Pt 2 (2024): 117283.

[169]

T. Lan, B. Chen, X. Hu, et al., “Tianhuang Formula Ameliorates Liver Fibrosis by Inhibiting CCL2-CCR2 a Xis and MAPK/NF-κB Signaling Pathway,” Journal of Ethnopharmacology 321 (2024): 117516.

[170]

X. J. Li, J. R. Qu, Y. H. Zhang, and R. P. Liu, “The Dual Function of cGAS-STING Signaling Axis in Liver Diseases,” Acta Pharmacologica Sinica 45, no. 6 (2024): 1115–1129.

[171]

J. Qu, Y. Cai, F. Li, X. Li, and R. Liu, “Potential Therapeutic Strategies for Colitis and Colon Cancer: Bidirectional Targeting STING Pathway,” EBioMedicine 111 (2024): 105491.

[172]

Y. Cai, S. Li, Y. Yang, et al., “Intestinal Epithelial Damage-derived mtDNA Activates STING-IL12 Axis in Dendritic Cells to Promote Colitis,” Theranostics 14, no. 11 (2024): 4393–4410.

[173]

W. Luo, G. Xu, Z. Song, et al., “Licorice Extract Inhibits the cGAS-STING Pathway and Protects Against Non-alcoholic Steatohepatitis,” Frontiers in Pharmacology 14 (2023): 1160445.

[174]

J.-W. Deng, S. Yuan, L.-P. Shi, et al., “Integration of Network Pharmacology and Serum Medicinal Chemistry to Investigate the Pharmacological Mechanisms of QiZhuYangGan Decoction in the Treatment of Hepatic Fibrosis,” Journal of Ethnopharmacology 323 (2024): 117730.

[175]

C. Shao, H. Xu, X. Sun, et al., “Jiawei Taohe Chengqi Decoction Inhibition of the Notch Signal Pathway Affects Macrophage Reprogramming to Inhibit HSCs Activation for the Treatment of Hepatic Fibrosis,” Journal of Ethnopharmacology 321 (2024): 117486.

[176]

Y. Zheng, S. Ji, X. Li, and L. Wen, “Qijia rougan Formula Ameliorates ECM Deposition in Hepatic Fibrosis by Regulating the JAK1/STAT6-microRNA-23a Feedback Loop in Macrophage M2 Polarization,” Biomedicine & Pharmacotherapy 168 (2023): 115794.

[177]

Z. Ma, X. Xue, J. Bai, et al., “Si-Wu-Tang Ameliorates Bile Duct Ligation-induced Liver Fibrosis via Modulating Immune Environment,” Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie 155 (2022): 113834.

[178]

Z. Ma, K. Xie, X. Xue, et al., “Si-Wu-Tang Attenuates Hepatocyte PANoptosis and M1 Polarization of Macrophages in Non-alcoholic Fatty Liver Disease by Influencing the Intercellular Transfer of mtDNA,” Journal of Ethnopharmacology 328 (2024): 118057.

[179]

B. O. Akcora, G. Storm, and R. Bansal, “Inhibition of Canonical WNT Signaling Pathway by Beta-catenin/CBP Inhibitor ICG-001 Ameliorates Liver Fibrosis in Vivo Through Suppression of Stromal CXCL12,” Biochimica Et Biophysica Acta, Molecular Basis of Disease 1864, no. 3 (2018): 804–818.

[180]

Y. Li, Z. Ma, M. Ding, et al., “Chuanxiong Rhizoma Extracts Prevent Cholestatic Liver Injury by Targeting H3K9ac-mediated and Cholangiocyte-derived Secretory Protein PAI-1 and FN,” Chinese Journal of Natural Medicines 21, no. 9 (2023): 694–709.

[181]

K. Kimura, T. Kanto, S. Shimoda, et al., “Safety, Tolerability, and Anti-fibrotic Efficacy of the CBP/Beta-catenin Inhibitor PRI-724 in Patients With hepatitis C and B Virus-induced Liver Cirrhosis: An Investigator-initiated, Open-label, Non-randomised, Multicentre, Phase 1/2a Study,” EBioMedicine 80 (2022): 104069.

[182]

X. Xu, Y. Guo, X. Luo, et al., “Hydronidone Ameliorates Liver Fibrosis by Inhibiting Activation of Hepatic Stellate Cells via Smad7-mediated Degradation of TGFbetaRI,” Liver International 43, no. 11 (2023): 2523–2537.

[183]

X. Cai, X. Liu, W. Xie, et al., “Hydronidone for the Treatment of Liver Fibrosis Related to Chronic Hepatitis B: A Phase 2 Randomized Controlled Trial,” Clinical Gastroenterology and Hepatology 21, no. 7 (2023): 1893–1901 e7.

[184]

S. Redenšek Trampuž, S. van Riet, N. Å, and M. Ingelman-Sundberg, “Mechanisms of 5-HT Receptor Antagonists in the Regulation of Fibrosis in a 3D human Liver Spheroid Model,” Scientific Reports 14, no. 1 (2024): 1396.

[185]

X. Y. Zhou, Z. Xu, X. Liu, et al., “Bifunctional LYTAC Mediates Hepatocytes-Hepatic Stellate Cells Crosstalk by Regulating 5-HT(2A) Receptor Degradation and Antagonism to Synergistically Ameliorate Hepatic Fibrosis,” Journal of the American Chemical Society 147, no. 48 (2025): 44162–44174.

[186]

R. M. Hussein, M. M. Anwar, H. S. Farghaly, and M. A. Kandeil, “Gallic Acid and Ferulic Acid Protect the Liver From Thioacetamide-induced Fibrosis in Rats via Differential Expression of miR-21, miR-30 and miR-200 and Impact on TGF-beta1/Smad3 Signaling,” Chemico-Biological Interactions 324 (2020): 109098.

[187]

M. Guo, Z. Wang, J. Dai, et al., “Glycyrrhizic Acid Alleviates Liver Fibrosis in Vitro and in Vivo via a Ctivating CUGBP1-mediated IFN-γ/STAT1/Smad7 Pathway,” Phytomedicine: International Journal of Phytotherapy and Phytopharmacology 112 (2023): 154587.

[188]

J. H. Yang, S. C. Kim, K. M. Kim, et al., “Isorhamnetin Attenuates Liver Fibrosis by Inhibiting TGF-β/Smad Signal Ing and Relieving Oxidative Stress,” European Journal of Pharmacology 783 (2016): 92–102.

[189]

Z. Li, Z. Wang, F. Dong, et al., “Germacrone Attenuates Hepatic Stellate Cells Activation and Liver Fibrosis via Regulating Multiple Signaling Pathways,” Frontiers in Pharmacology 12 (2021): 745561.

[190]

Y. Zhang, B. Cai, Y. Li, et al., “Identification of Linderalactone as a Natural Inhibitor of SHP2 to Ameliorate CCl(4)-induced Liver Fibrosis,” Frontiers in Pharmacology 14 (2023): 1098463.

[191]

Y. Li, F. Li, M. Ding, et al., “Chuanxiong Rhizoma Extracts Prevent Liver Fibrosis via Targeting CTCF-c-MYC-H19 Pathway,” Chinese Herbal Medicines 16, no. 1 (2024): 82–93.

[192]

J. Li, X. Li, W. Xu, et al., “Antifibrotic Effects of Luteolin on Hepatic Stellate Cells and Liver Fibrosis by Targeting AKT/mTOR/p70S6K and TGFbeta/Smad Signalling Pathways,” Liver International 35, no. 4 (2015): 1222–1233.

[193]

Q. Chen, L. Chen, D. Kong, J. Shao, L. Wu, and S. Zheng, “Dihydroartemisinin Alleviates Bile Duct Ligation-induced Liver Fibrosis and Hepatic Stellate Cell Activation by Interfering With the PDGF-betaR/ERK Signaling Pathway,” International Immunopharmacology 34 (2016): 250–258.

[194]

R. Wang, F. Liu, P. Chen, et al., “Gomisin D Alleviates Liver Fibrosis Through Targeting PDGFRbeta in Hepatic Stellate Cells,” International Journal of Biological Macromolecules 235 (2023): 123639.

[195]

J. Feng, C. Wang, T. Liu, et al., “Procyanidin B2 Inhibits the Activation of Hepatic Stellate Cells and Angiogenesis via the Hedgehog Pathway During Liver Fibrosis,” Journal of Cellular and Molecular Medicine 23, no. 9 (2019): 6479–6493.

[196]

X. Zhu, S. Ye, D. Yu, et al., “Physalin B Attenuates Liver Fibrosis via Suppressing LAP2alpha-HDAC1-mediated Deacetylation of the Transcription Factor GLI1 and Hepatic Stellate Cell Activation,” British Journal of Pharmacology 178, no. 17 (2021): 3428–3447.

[197]

T. Greuter, U. Yaqoob, C. Gan, et al., “Mechanotransduction-induced Glycolysis Epigenetically Regulates a CXCL1-dominant Angiocrine Signaling Program in Liver Sinusoidal Endothelial Cells in Vitro and in Vivo,” Journal of Hepatology 77, no. 3 (2022): 723–734.

[198]

F. Zhang, S. Lu, J. He, et al., “Ligand Activation of PPARgamma by Ligustrazine Suppresses Pericyte Functions of Hepatic Stellate Cells via SMRT-Mediated Transrepression of HIF-1alpha,” Theranostics 8, no. 3 (2018): 610–626.

[199]

T. Lan, L. Zhuang, S. Li, G. Yang, Y. Xuan, and J. Guo, “Polydatin Attenuates Hepatic Stellate Cell Proliferation and Liver Fibrosis by Suppressing Sphingosine Kinase 1,” Biomedicine & Pharmacotherapy 130 (2020): 110586.

[200]

X. Zhao, Y. Yang, H. Yu, et al., “Polydatin Inhibits ZEB1-invoked Epithelial-mesenchymal Transition in Fructose-induced Liver Fibrosis,” Journal of Cellular and Molecular Medicine 24, no. 22 (2020): 13208–13222.

[201]

H. Zhao, Z. Wang, F. Tang, et al., “Carnosol-mediated Sirtuin 1 Activation Inhibits Enhancer of Zeste Homolog 2 to Attenuate Liver Fibrosis,” Pharmacological Research 128 (2018): 327–337.

[202]

D. Kong, Z. Zhang, L. Chen, et al., “Curcumin Blunts Epithelial-mesenchymal Transition of Hepatocytes to Alleviate Hepatic Fibrosis Through Regulating Oxidative Stress and Autophagy,” Redox Biology 36 (2020): 101600.

[203]

M. Nouri-Vaskeh, A. Malek Mahdavi, H. Afshan, L. Alizadeh, and M. Zarei, “Effect of Curcumin Supplementation on Disease Severity in Patients With Liver Cirrhosis: A Randomized Controlled Trial,” Phytotherapy Research 34, no. 6 (2020): 1446–1454.

[204]

H. Gerami, H. Mozaffari-Khosravi, A. Mansour, et al., “Effect of Nano-curcumin Supplementation on Liver Fibrosis in Patients With NAFLD-associated Fibrosis: A Double-blind Randomized Controlled Trial,” Scientific Reports 15, no. 1 (2025): 38043.

[205]

H. M. Xiao, M. J. Shi, J. M. Jiang, et al., “Efficacy and Safety of AnluoHuaxian Pills on Chronic hepatitis B With Normal or Minimally Elevated Alanine Transaminase and Early Liver Fibrosis: A Randomized Controlled Trial,” Journal of Ethnopharmacology 293 (2022): 115210.

[206]

X. M. Li, J. H. Peng, Z. L. Sun, et al., “Chinese Medicine CGA Formula Ameliorates DMN-induced Liver Fibrosis in Rats via Inhibiting MMP2/9, TIMP1/2 and the TGF-beta/Smad Signaling Pathways,” Acta Pharmacologica Sinica 37, no. 6 (2016): 783–793.

[207]

Y. Chen, R. Li, N. Hu, et al., “Baihe Wuyao Decoction Ameliorates CCl(4)-induced Chronic Liver Injury and Liver Fibrosis in Mice Through Blocking TGF-beta1/Smad2/3 Signaling, Anti-inflammation and Anti-oxidation Effects,” Journal of Ethnopharmacology 263 (2020): 113227.

[208]

X. F. Chen, Y. Wang, S. Ji, et al., “Hepatoprotective Efficacy and Interventional Mechanism of Qijia Rougan Decoction in Liver Fibrosis,” Frontiers in Pharmacology 13 (2022): 911250.

[209]

Y. Zhou, R. Wu, F.-F. Cai, et al., “Xiaoyaosan Decoction Alleviated Rat Liver Fibrosis via the TGFβ/Smad a nd Akt/FoxO3 Signaling Pathways Based on Network Pharmacology Analysis,” Journal of Ethnopharmacology 264 (2021): 113021.

[210]

Y. Yang, M. Sun, W. Li, et al., “Rebalancing TGF-beta/Smad7 Signaling via Compound kushen Injection in Hepatic Stellate Cells Protects Against Liver Fibrosis and Hepatocarcinogenesis,” Clinical and Translational Medicine 11, no. 7 (2021): e410.

[211]

Y. Huang, Z.-L. Wang, Y. He, L.-M. Ye, W.-Q. Guo, and J.-J. Zhang, “Jiawei Taohe Chengqi Decoction Attenuates Hepatic Fibrosis by Preventi Ng Activation of HSCs Through Regulating Src/ERK/Smad3 Signal Pathway,” Journal of Ethnopharmacology 305 (2023): 116059.

[212]

H. Liu, L. Wang, L. Dai, F. Feng, and Y. Xiao, “CaMK II/Ca2+ Dependent Endoplasmic Reticulum Stress Mediates Apoptosis of Hepatic Stellate Cells Stimulated by Transforming Growth Factor Beta 1,” International Journal of Biological Macromolecules 172 (2021): 321–329.

[213]

H. Liu, L. Dai, M. Wang, F. Feng, and Y. Xiao, “Tunicamycin Induces Hepatic Stellate Cell Apoptosis through Calpain-2/Ca(2 +)-Dependent Endoplasmic Reticulum Stress Pathway,” Frontiers in Cell and Developmental Biology 9 (2021): 684857.

[214]

X. Zheng, W. Ma, R. Sun, et al., “Butaselen Prevents Hepatocarcinogenesis and Progression Through Inhibiting Thioredoxin Reductase Activity,” Redox Biology 14 (2018): 237–249.

[215]

C. H. Chen, M. F. Chen, S. J. Huang, et al., “Saikosaponin a Induces Apoptosis Through Mitochondria-Dependent Pathway in Hepatic Stellate Cells,” American Journal of Chinese Medicine 45, no. 2 (2017): 351–368.

[216]

M. Bian, J. He, H. Jin, et al., “Oroxylin A Induces Apoptosis of Activated Hepatic Stellate Cells Through Endoplasmic Reticulum Stress,” Apoptosis 24, no. 11-12 (2019): 905–920.

[217]

S. Yuan, C. Wei, G. Liu, et al., “Sorafenib Attenuates Liver Fibrosis by Triggering Hepatic Stellate Cell Ferroptosis via HIF-1alpha/SLC7A11 Pathway,” Cell Proliferation 55, no. 1 (2022): e13158.

[218]

G. Liu, C. Wei, S. Yuan, et al., “Wogonoside Attenuates Liver Fibrosis by Triggering Hepatic Stellate ce Ll Ferroptosis Through SOCS1/P53/SLC7A11 Pathway,” Phytotherapy Research: PTR 36, no. 11 (2022): 4230–4243.

[219]

Z. Kong, R. Liu, and Y. Cheng, “Artesunate Alleviates Liver Fibrosis by Regulating Ferroptosis Signaling Pathway,” Biomedicine & Pharmacotherapy 109 (2019): 2043–2053.

[220]

X. Li, F. Jiang, Y. Hu, et al., “Schisandrin B Promotes Hepatic Stellate Cell Ferroptosis via Wnt Pathway-Mediated Ly6Clo Macrophages,” Journal of Agricultural and Food Chemistry 71, no. 45 (2023): 17295–17307.

[221]

S. Huang, Y. Wang, S. Xie, et al., “Isoliquiritigenin Alleviates Liver Fibrosis Through Caveolin-1-mediate D Hepatic Stellate Cells Ferroptosis in Zebrafish and Mice,” Phytomedicine 101 (2022): 154117.

[222]

N. Liu, M. Liu, M. Jiang, et al., “Isoliquiritigenin Alleviates the Development of Alcoholic Liver Fibrosis by Inhibiting ANXA2,” Biomedicine & Pharmacotherapy 159 (2023): 114173.

[223]

A. K. Shendge, T. Basu, S. Panja, D. Chaudhuri, and N. Mandal, “An Ellagic Acid Isolated From Clerodendrum Viscosum Leaves Ameliorates Iron-overload Induced Hepatotoxicity in Swiss Albino Mice Through Inhibition of Oxidative Stress and the Apoptotic Pathway,” Biomedicine & Pharmacotherapy 106 (2018): 454–465.

[224]

L. Li, K. Wang, R. Jia, et al., “Ferroportin-dependent Ferroptosis Induced by Ellagic Acid Retards Liver Fibrosis by Impairing the SNARE Complexes Formation,” Redox Biology 56 (2022): 102435.

[225]

J. Q. JL, L. Wang, Y. Li, et al., “Disturbance of Cytoskeleton Induced by Ligustilide Promotes Hepatic Stellate Cell Senescence and Ameliorates Liver Fibrosis,” Theranostics 15, no. 16 (2025): 8049–8067.

[226]

J. Zhao, D. Bai, L. Qi, et al., “The Flavonoid GL-V9 Alleviates Liver Fibrosis by Triggering Senescence by Regulating the Transcription Factor GATA4 in Activated Hepatic Stellate Cells,” British Journal of Pharmacology 180, no. 8 (2023): 1072–1089.

[227]

K. Du, R. Maeso-Díaz, S. H. Oh, et al., “Targeting YAP-mediated HSC Death Susceptibility and Senescence for Treatment of Liver Fibrosis,” Hepatology 77, no. 6 (2023): 1998–2015.

[228]

Y. Sun, J. Weng, X. Chen, et al., “Oroxylin A Activates Ferritinophagy to Induce Hepatic Stellate Cell Senescence Against Hepatic Fibrosis by Regulating cGAS-STING Pathway,” Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie 162 (2023): 114653.

[229]

D. Zhao, Y. Gao, Y. Su, et al., “Oroxylin A Regulates cGAS DNA Hypermethylation Induced by Methionine Metabolism to Promote HSC Senescence,” Pharmacological Research 187 (2023): 106590.

[230]

L. Cheng, J. Shi, H. Peng, R. Tong, Y. Hu, and D. Yu, “Probiotics and Liver Fibrosis: An Evidence-based Review of the Latest Research,” Journal of Functional Foods 109 (2023): 105773.

[231]

R. Maslennikov, E. Poluektova, O. Zolnikova, et al., “Gut Microbiota and Bacterial Translocation in the Pathogenesis of Liver Fibrosis,” International Journal of Molecular Sciences 24, no. 22 (2023): 16502.

[232]

Y. Liu, K. Chen, F. Li, et al., “Probiotic Lactobacillus Rhamnosus GG Prevents Liver Fibrosis through Inhibiting Hepatic Bile Acid Synthesis and Enhancing Bile Acid Excretion in Mice,” Hepatology (Baltimore, Md) 71, no. 6 (2020): 2050–2066.

[233]

C. Grander, T. E. Adolph, V. Wieser, et al., “Recovery of Ethanol-induced Akkermansia Muciniphila Depletion Ameliorates Alcoholic Liver Disease,” Gut 67, no. 5 (2018): 891–901.

[234]

C. L. Hsu and B. Schnabl, “The Gut-liver Axis and Gut Microbiota in Health and Liver Disease,” Nature Reviews Microbiology 21, no. 11 (2023): 719–733.

[235]

J. Trebicka, J. Macnaughtan, B. Schnabl, D. L. Shawcross, and J. S. Bajaj, “The Microbiota in Cirrhosis and Its Role in Hepatic Decompensation,” Journal of Hepatology 75, no. Suppl 1 (2021): S67–s81.

[236]

Q. Zhao, M. Y. Dai, R. Y. Huang, et al., “Parabacteroides Distasonis Ameliorates Hepatic Fibrosis Potentially via Modulating Intestinal Bile Acid Metabolism and Hepatocyte Pyroptosis in Male Mice,” Nature Communications 14, no. 1 (2023): 1829.

[237]

N. M. Hany, S. Eissa, M. Basyouni, et al., “Modulation of Hepatic Stellate Cells by Mutaflor® Probiotic in Non-alcoholic Fatty Liver Disease Management,” Journal of Translational Medicine 20, no. 1 (2022): 342.

[238]

M. H. Mohamad Nor, N. Ayob, N. M. Mokhtar, et al., “The Effect of Probiotics (MCP® BCMC® Strains) on Hepatic Steatosis, Small Intestinal Mucosal Immune Function, and Intestinal Barrier in Patients With Non-Alcoholic Fatty Liver Disease,” Nutrients 13, no. 9 (2021): 3192.

[239]

X. Fang, F. Gao, Q. Yao, et al., “Pooled Analysis of Mesenchymal Stromal Cell-Derived Extracellular Vesicle Therapy for Liver Disease in Preclinical Models,” Journal of Personalized Medicine 13, no. 3 (2023): 441.

[240]

P. Andreone, L. Catani, C. Margini, et al., “Reinfusion of Highly Purified CD133+ Bone Marrow-derived Stem/Progenitor Cells in Patients With End-stage Liver Disease: A Phase I Clinical Trial,” Digestive and Liver Disease 47, no. 12 (2015): 1059–1066.

[241]

P. N. Newsome, R. Fox, A. L. King, et al., “Granulocyte Colony-stimulating Factor and Autologous CD133-positive Stem-cell Therapy in Liver Cirrhosis (REALISTIC): An Open-label, Randomised, Controlled Phase 2 Trial,” The Lancet Gastroenterology & Hepatology 3, no. 1 (2018): 25–36.

[242]

P. N. Brennan, M. MacMillan, T. Manship, et al., “Study Protocol: A Multicentre, Open-label, Parallel-group, Phase 2, Randomised Controlled Trial of Autologous Macrophage Therapy for Liver Cirrhosis (MATCH),” BMJ Open 11, no. 11 (2021): e053190.

[243]

K. Cusi, B. Orsak, F. Bril, et al., “Long-Term Pioglitazone Treatment for Patients with Nonalcoholic Steatohepatitis and Prediabetes or Type 2 Diabetes Mellitus: A Randomized Trial,” Annals of Internal Medicine 165, no. 5 (2016): 305–315.

[244]

E. J. Lawitz, B. R. Bhandari, P. J. Ruane, et al., “Fenofibrate Mitigates Hypertriglyceridemia in Nonalcoholic Steatohepatitis Patients Treated with Cilofexor/Firsocostat,” Clinical Gastroenterology and Hepatology: The Official Clinical Practice Journal of the American Gastroenterological Association 21, no. 1 (2023): 143–152.e3.

[245]

K. Böttcher and M. Pinzani, “Pathophysiology of Liver Fibrosis and the Methodological Barriers to the Development of Anti-fibrogenic Agents,” Advanced Drug Delivery Reviews 121 (2017): 3–8.

[246]

X. Ai, P. Yu, L. Peng, et al., “Berberine: A Review of Its Pharmacokinetics Properties and Therapeutic Potentials in Diverse Vascular Diseases,” Frontiers in Pharmacology 12 (2021): 762654.

[247]

M. Rizzo, A. Colletti, P. E. Penson, et al., “Nutraceutical Approaches to Non-alcoholic Fatty Liver Disease (NAFLD): A Position Paper From the International Lipid Expert Panel (ILEP),” Pharmacological Research 189 (2023): 106679.

[248]

X. Zeng, D. Huang, Z. Zhu, et al., “Mechanism-guided Drug Development and Treatment for Liver Fibrosis: A Clinical Perspective,” Frontiers in Pharmacology 16 (2025): 1574385.

[249]

B. A. Priego-Parra, R. Gallego-Durán, B. M. Román-Calleja, J. A. Velarde-Ruiz Velasco, M. Romero-Gómez, and J. Gracia-Sancho, “Advancing Precision Medicine in Metabolic Dysfunction-associated Steatotic Liver Disease,” Trends in Endocrinology & Metabolism 36, no. 11 (2025): 1000–1013.

[250]

G. Codotto, B. Blarasin, C. Tiribelli, C. Bellarosa, and D. Licastro, “Decoding Liver Fibrosis: How Omics Technologies and Innovative Modeling Can Guide Precision Medicine,” International Journal of Molecular Sciences 26, no. 6 (2025): 2658.

[251]

A. Caddeo and S. Romeo, “Precision Medicine and Nucleotide-based Therapeutics to Treat Steatotic Liver Disease,” Clinical and Molecular Hepatology 31, no. Suppl (2025): S76–s93.

[252]

Y. Iwakiri, “Unlocking the Role of Liver Sinusoidal Endothelial Cells: Key Players in Liver Fibrosis: Editorial on “Liver Sinusoidal Endothelial Cell: An Important yet Often Overlooked Player in the Liver Fibrosis”,” Clinical and Molecular Hepatology 30, no. 4 (2024): 673–676.

[253]

J. Qu, L. Wang, and X. Li, “Correspondence to Editorial on “Liver Sinusoidal Endothelial Cell: An Important yet Often Overlooked Player in the Liver Fibrosis”,” Clinical and Molecular Hepatology 30, no. 4 (2024): 1002–1004.

[254]

J. Qu, L. Wang, Y. Li, and X. Li, “Liver Sinusoidal Endothelial Cell: An Important yet Often Overlooked Player in the Liver Fibrosis,” Clinical and Molecular Hepatology 30, no. 3 (2024): 303–325.

[255]

C. Airola, M. Pallozzi, L. Cerrito, et al., “Microvascular Thrombosis and Liver Fibrosis Progression: Mechanisms and Clinical Applications,” Cells 12, no. 13 (2023): 1712.

[256]

Y. N. Zhou, M. Y. Sun, Y. P. Mu, et al., “Xuefuzhuyu Decoction Inhibition of Angiogenesis Attenuates Liver Fibrosis Induced by CCl(4) in Mice,” Journal of Ethnopharmacology 153, no. 3 (2014): 659–666.

[257]

C. Fu, Y. Zhang, W. J. Xi, et al., “Dahuang Zhechong Pill Attenuates Hepatic Sinusoidal Capillarization in Liver Cirrhosis and Hepatocellular Carcinoma Rat Model via the MK/Int Egrin Signaling Pathway,” Journal of Ethnopharmacology 308 (2023): 116191.

[258]

L. Wang, J. Qu, J. Li, et al., “Si-Wu-Tang Improves Liver Fibrosis by Restoring Liver Sinusoidal Endothelial Cell Functionality and Reducing Communication With Hepatic Stellate Cells,” Chinese Medicine 19, no. 1 (2024): 179.

[259]

M. E. Delgado, B. I. Cárdenas, N. Farran, and M. Fernandez, “Metabolic Reprogramming of Liver Fibrosis,” Cells 10, no. 12 (2021): 3604.

[260]

J. Zhang, Z. Xie, X. Zhu, et al., “New Insights Into Therapeutic Strategies for Targeting Hepatic Macrophages to Alleviate Liver Fibrosis,” International Immunopharmacology 158 (2025): 114864.

[261]

M. Amir, E. Zhao, L. Fontana, et al., “Inhibition of Hepatocyte Autophagy Increases Tumor Necrosis Factor-dependent Liver Injury by Promoting Caspase-8 Activation,” Cell Death and Differentiation 20, no. 7 (2013): 878–887.

[262]

W. Peng, S. Cheng, Z. Bao, et al., “Advances in the Research of Nanodrug Delivery System for Targeted Treatment of Liver Fibrosis,” Biomedicine & Pharmacotherapy 137 (2021): 111342.

[263]

Y. Zhang, L. Wang, J. Shao, et al., “Nano-calcipotriol as a Potent Anti-hepatic Fibrosis Agent,” MedComm 4, no. 5 (2023): e354.

[264]

T. Yamazaki, A. J. Gunderson, M. Gilchrist, et al., “Galunisertib plus Neoadjuvant Chemoradiotherapy in Patients With Locally Advanced Rectal Cancer: A Single-arm, Phase 2 Trial,” The Lancet Oncology 23, no. 9 (2022): 1189–1200.

[265]

E. Panzarini, S. Leporatti, B. A. Tenuzzo, et al., “Therapeutic Effect of Polymeric Nanomicelles Formulation of LY2157299-Galunisertib on CCl(4)-Induced Liver Fibrosis in Rats,” Journal of Personalized Medicine 12, no. 11 (2022): 1812.

[266]

S. Luo, Y. Yang, T. Zhao, et al., “Albumin-Based Silibinin Nanocrystals Targeting Activated Hepatic Stell Ate Cells for Liver Fibrosis Therapy,” ACS Applied Materials & Interfaces 15, no. 6 (2023): 7747–7758.

[267]

L. Wang, J. Zhou, J. Wang, et al., “Hepatic Stellate Cell-Targeting Micelle Nanomedicine for Early Diagnos Is and Treatment of Liver Fibrosis,” Advanced Healthcare Materials 13, no. 12 (2024): e2303710.

[268]

J. Luo, Z. Zhang, Y. Zeng, Y. Dong, and L. Ma, “Co-encapsulation of Collagenase Type I and Silibinin in Chondroitin Sulfate Coated Multilayered Nanoparticles for Targeted Treatment of Liver Fibrosis,” Carbohydrate Polymers 263 (2021): 117964.

[269]

X. Wang, W. Zhang, S. Zeng, L. Wang, and B. Wang, “Collagenase Type I and Probucol-Loaded Nanoparticles Penetrate the Ext Racellular Matrix to Target Hepatic Stellate Cells for Hepatic Fibrosis Therapy,” Acta Biomaterialia 175 (2024): 262–278.

[270]

Q.-Q. Fan, C.-L. Zhang, J.-B. Qiao, et al., “Extracellular Matrix-penetrating Nanodrill Micelles for Liver Fibrosis Therapy,” Biomaterials 230 (2020): 119616.

[271]

L. Zhou, Q. Liang, Y. Li, et al., “Collagenase-I Decorated co-delivery Micelles Potentiate Extracellular Matrix Degradation and Hepatic Stellate Cell Targeting for Liver Fibrosis Therapy,” Acta Biomaterialia 152 (2022): 235–254.

[272]

J. Luo, P. Zhang, T. Zhao, et al., “Golgi Apparatus-Targeted Chondroitin-Modified Nanomicelles Suppress Hepatic Stellate Cell Activation for the Management of Liver Fibrosis,” ACS Nano 13, no. 4 (2019): 3910–3923.

[273]

J. Shinn, S. Park, S. Lee, et al., “Antioxidative Hyaluronic Acid-Bilirubin Nanomedicine Targeting Activated Hepatic Stellate Cells for Anti-Hepatic-Fibrosis Therapy,” ACS Nano 18, no. 6 (2024): 4704–4716.

[274]

Z. Zhang, C. Wang, Y. Zha, et al., “Corona-directed Nucleic Acid Delivery Into Hepatic Stellate Cells for Liver Fibrosis Therapy,” ACS Nano 9, no. 3 (2015): 2405–2419.

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