References
- Baik SJ, Kim TH, Yoo K, et al. Decreased S100B expression in chronic liver diseases. Korean J Intern Med 2016 Jun 3 [Epub]. http://doi.org/10.3904/kjim.2015.296.
- Friedman SL. Mechanisms of hepatic fibrogenesis. Gastroenterology 2008;134:1655-1669. https://doi.org/10.1053/j.gastro.2008.03.003
- Ueno T, Sata M, Sakata R, et al. Hepatic stellate cells and intralobular innervation in human liver cirrhosis. Hum Pathol 1997;28:953-959. https://doi.org/10.1016/S0046-8177(97)90011-3
- Hellerbrand C, Stefanovic B, Giordano F, Burchardt ER, Brenner DA. The role of TGFbeta1 in initiating hepatic stellate cell activation in vivo. J Hepatol 1999;30:77-87. https://doi.org/10.1016/S0168-8278(99)80010-5
- Bataller R, Brenner DA. Liver fibrosis. J Clin Invest 2005;115:209-218. https://doi.org/10.1172/JCI24282
- Krizhanovsky V, Yon M, Dickins RA, et al. Senescence of activated stellate cells limits liver fibrosis. Cell 2008;134:657-667. https://doi.org/10.1016/j.cell.2008.06.049
- Mormone E, George J, Nieto N. Molecular pathogenesis of hepatic fibrosis and current therapeutic approaches. Chem Biol Interact 2011;193:225-231. https://doi.org/10.1016/j.cbi.2011.07.001
- Nieto N. Oxidative-stress and IL-6 mediate the fibrogenic effects of [corrected] Kupffer cells on stellate cells. Hepatology 2006;44:1487-1501. https://doi.org/10.1002/hep.21427
- Kisseleva T, Brenner DA. Role of hepatic stellate cells in fibrogenesis and the reversal of fibrosis. J Gastroenterol Hepatol 2007;22 Suppl 1:S73-S78. https://doi.org/10.1111/j.1440-1746.2006.04658.x
- Sanz-Cameno P, Medina J, Garcia-Buey L, et al. Enhanced intrahepatic inducible nitric oxide synthase expression and nitrotyrosine accumulation in primary biliary cirrhosis and autoimmune hepatitis. J Hepatol 2002;37:723-729. https://doi.org/10.1016/S0168-8278(02)00266-0
- Zhan SS, Jiang JX, Wu J, et al. Phagocytosis of apoptotic bodies by hepatic stellate cells induces NADPH oxidase and is associated with liver fibrosis in vivo. Hepatology 2006;43:435-443. https://doi.org/10.1002/hep.21093
- Iwakiri Y. Nitric oxide in liver fibrosis: the role of inducible nitric oxide synthase. Clin Mol Hepatol 2015;21:319-325. https://doi.org/10.3350/cmh.2015.21.4.319
- De Minicis S, Brenner DA. NOX in liver fibrosis. Arch Biochem Biophys 2007;462:266-272. https://doi.org/10.1016/j.abb.2007.04.016
-
Hayashi H, Sakai T. Biological significance of local TGF-
$\beta$ activation in liver diseases. Front Physiol 2012;3:12. - Bataller R, Sancho-Bru P, Gines P, et al. Activated human hepatic stellate cells express the renin-angiotensin system and synthesize angiotensin II. Gastroenterology 2003;125:117-125. https://doi.org/10.1016/S0016-5085(03)00695-4
- Wasmuth HE, Trautwein C. CB1 cannabinoid receptor antagonism: a new strategy for the treatment of liver fibrosis. Hepatology 2007;45:543-544. https://doi.org/10.1002/hep.21527
- Julien B, Grenard P, Teixeira-Clerc F, et al. Antifibrogenic role of the cannabinoid receptor CB2 in the liver. Gastroenterology 2005;128:742-755. https://doi.org/10.1053/j.gastro.2004.12.050
- Marra F, Bertolani C. Adipokines in liver diseases. Hepatology 2009;50:957-969. https://doi.org/10.1002/hep.23046
- Bomble M, Tacke F, Rink L, Kovalenko E, Weiskirchen R. Analysis of antigen-presenting functionality of cultured rat hepatic stellate cells and transdifferentiated myofibroblasts. Biochem Biophys Res Commun 2010;396:342-347. https://doi.org/10.1016/j.bbrc.2010.04.094
- Schuppan D, Kim YO. Evolving therapies for liver fibrosis. J Clin Invest 2013;123:1887-1901. https://doi.org/10.1172/JCI66028
- Thabut D, Shah V. Intrahepatic angiogenesis and sinusoidal remodeling in chronic liver disease: new targets for the treatment of portal hypertension? J Hepatol 2010;53:976-980. https://doi.org/10.1016/j.jhep.2010.07.004
- Muhanna N, Abu Tair L, Doron S, et al. Amelioration of hepatic fibrosis by NK cell activation. Gut 2011;60:90-98. https://doi.org/10.1136/gut.2010.211136
- Tiggelman AM, Boers W, Linthorst C, Brand HS, Sala M, Chamuleau RA. Interleukin-6 production by human liver (myo)fibroblasts in culture: evidence for a regulatory role of LPS, IL-1 beta and TNF alpha. J Hepatol 1995;23:295-306.
- Schwabe RF, Bataller R, Brenner DA. Human hepatic stellate cells express CCR5 and RANTES to induce proliferation and migration. Am J Physiol Gastrointest Liver Physiol 2003;285:G949-G958. https://doi.org/10.1152/ajpgi.00215.2003
- Li Z, Yang S, Lin H, et al. Probiotics and antibodies to TNF inhibit inflammatory activity and improve nonalcoholic fatty liver disease. Hepatology 2003;37:343-350. https://doi.org/10.1053/jhep.2003.50048
- Wasmuth HE, Tacke F, Trautwein C. Chemokines in liver inflammation and fibrosis. Semin Liver Dis 2010;30:215-225. https://doi.org/10.1055/s-0030-1255351
- Jiang JX, Venugopal S, Serizawa N, et al. Reduced nicotinamide adenine dinucleotide phosphate oxidase 2 plays a key role in stellate cell activation and liver fibrogenesis in vivo. Gastroenterology 2010;139:1375-1384. https://doi.org/10.1053/j.gastro.2010.05.074
- Jiang JX, Mikami K, Venugopal S, Li Y, Torok NJ. Apoptotic body engulfment by hepatic stellate cells promotes their survival by the JAK/STAT and Akt/NF-kappaB-dependent pathways. J Hepatol 2009;51:139-148. https://doi.org/10.1016/j.jhep.2009.03.024
-
Jeong WI, Park O, Suh YG, et al. Suppression of innate immunity (natural killer cell/interferon-
$\gamma$ ) in the advanced stages of liver fibrosis in mice. Hepatology 2011;53:1342-1351. https://doi.org/10.1002/hep.24190 - Hellerbrand, Wang SC, Tsukamoto H, Brenner DA, Rippe RA. Expression of intracellular adhesion molecule 1 by activated hepatic stellate cells. Hepatology 1996;24:670-676. https://doi.org/10.1002/hep.510240333
- Knittel T, Dinter C, Kobold D, et al. Expression and regulation of cell adhesion molecules by hepatic stellate cells (HSC) of rat liver: involvement of HSC in recruitment of inflammatory cells during hepatic tissue repair. Am J Pathol 1999;154:153-167. https://doi.org/10.1016/S0002-9440(10)65262-5
- Wynn TA, Ramalingam TR. Mechanisms of fibrosis: therapeutic translation for fibrotic disease. Nat Med 2012;18:1028-1040. https://doi.org/10.1038/nm.2807
- Wilson MS, Wynn TA. Pulmonary fibrosis: pathogenesis, etiology and regulation. Mucosal Immunol 2009;2:103-121. https://doi.org/10.1038/mi.2008.85
- Wynn TA, Cheever AW, Jankovic D, et al. An IL-12-based vaccination method for preventing fibrosis induced by schistosome infection. Nature 1995;376:594-596. https://doi.org/10.1038/376594a0
- Marra F, Aleffi S, Galastri S, Provenzano A. Mononuclear cells in liver fibrosis. Semin Immunopathol 2009;31:345-358. https://doi.org/10.1007/s00281-009-0169-0
- Zimmermann HW, Seidler S, Nattermann J, et al. Functional contribution of elevated circulating and hepatic non-classical CD14CD16 monocytes to inflammation and human liver fibrosis. PLoS One 2010;5:e11049. https://doi.org/10.1371/journal.pone.0011049
- Duffield JS, Forbes SJ, Constandinou CM, et al. Selective depletion of macrophages reveals distinct, opposing roles during liver injury and repair. J Clin Invest 2005;115:56-65. https://doi.org/10.1172/JCI200522675
- Miura K, Yang L, van Rooijen N, Ohnishi H, Seki E. Hepatic recruitment of macrophages promotes nonalcoholic steatohepatitis through CCR2. Am J Physiol Gastrointest Liver Physiol 2012;302:G1310-G1321. https://doi.org/10.1152/ajpgi.00365.2011
- Kisseleva T, Brenner DA. The phenotypic fate and functional role for bone marrow-derived stem cells in liver fibrosis. J Hepatol 2012;56:965-972. https://doi.org/10.1016/j.jhep.2011.09.021
- Albillos A, Lario M, Alvarez-Mon M. Cirrhosis-associated immune dysfunction: distinctive features and clinical relevance. J Hepatol 2014;61:1385-1396. https://doi.org/10.1016/j.jhep.2014.08.010
- Ubeda M, Munoz L, Borrero MJ, et al. Critical role of the liver in the induction of systemic inflammation in rats with preascitic cirrhosis. Hepatology 2010;52:2086-2095. https://doi.org/10.1002/hep.23961
- Kubes P, Mehal WZ. Sterile inflammation in the liver. Gastroenterology 2012;143:1158-1172. https://doi.org/10.1053/j.gastro.2012.09.008
- Song Y, Zhao Y, Wang F, Tao L, Xiao J, Yang C. Autophagy in hepatic fibrosis. Biomed Res Int 2014;2014:436242.
- Senoo H, Yoshikawa K, Morii M, Miura M, Imai K, Mezaki Y. Hepatic stellate cell (vitamin A-storing cell) and its relative: past, present and future. Cell Biol Int 2010;34:1247-1272. https://doi.org/10.1042/CBI20100321
- Thoen LF, Guimaraes EL, Dolle L, et al. A role for autophagy during hepatic stellate cell activation. J Hepatol 2011;55:1353-1360. https://doi.org/10.1016/j.jhep.2011.07.010
- Gressner AM, Polzar B, Lahme B, Mannherz HG. Induction of rat liver parenchymal cell apoptosis by hepatic myofibroblasts via transforming growth factor beta. Hepatology 1996;23:571-581.
- Gressner AM, Bachem MG. Molecular mechanisms of liver fibrogenesis: a homage to the role of activated fat-storing cells. Digestion 1995;56:335-346. https://doi.org/10.1159/000201257
- Derynck R, Zhang YE. Smad-dependent and Smad-independent pathways in TGF-beta family signalling. Nature 2003;425:577-584. https://doi.org/10.1038/nature02006
- Latella G, Vetuschi A, Sferra R, et al. Targeted disruption of Smad3 confers resistance to the development of dimethylnitrosamine-induced hepatic fibrosis in mice. Liver Int 2009;29:997-1009. https://doi.org/10.1111/j.1478-3231.2009.02011.x
- Dooley S, Hamzavi J, Ciuclan L, et al. Hepatocyte-specific Smad7 expression attenuates TGF-beta-mediated fibrogenesis and protects against liver damage. Gastroenterology 2008;135:642-659. https://doi.org/10.1053/j.gastro.2008.04.038
- Garzon R, Marcucci G, Croce CM. Targeting microRNAs in cancer: rationale, strategies and challenges. Nat Rev Drug Discov 2010;9:775-789. https://doi.org/10.1038/nrd3179
- Noetel A, Kwiecinski M, Elfimova N, Huang J, Odenthal M. MicroRNA are central players in anti- and profibrotic gene regulation during liver fibrosis. Front Physiol 2012;3:49.
- Roderburg C, Urban GW, Bettermann K, et al. Micro-RNA profiling reveals a role for miR-29 in human and murine liver fibrosis. Hepatology 2011;53:209-218. https://doi.org/10.1002/hep.23922
- Lakner AM, Steuerwald NM, Walling TL, et al. Inhibitory effects of microRNA 19b in hepatic stellate cell-mediated fibrogenesis. Hepatology 2012;56:300-310.
- Guimaraes EL, Empsen C, Geerts A, van Grunsven LA. Advanced glycation end products induce production of reactive oxygen species via the activation of NADPH oxidase in murine hepatic stellate cells. J Hepatol 2010;52:389-397.
- Benyon RC, Iredale JP, Goddard S, Winwood PJ, Arthur MJ. Expression of tissue inhibitor of metalloproteinases 1 and 2 is increased in fibrotic human liver. Gastroenterology 1996;110:821-831. https://doi.org/10.1053/gast.1996.v110.pm8608892
- Iredale JP, Benyon RC, Pickering J, et al. Mechanisms of spontaneous resolution of rat liver fibrosis. Hepatic stellate cell apoptosis and reduced hepatic expression of metalloproteinase inhibitors. J Clin Invest 1998;102:538-549. https://doi.org/10.1172/JCI1018
- Murphy FR, Issa R, Zhou X, et al. Inhibition of apoptosis of activated hepatic stellate cells by tissue inhibitor of metalloproteinase-1 is mediated via effects on matrix metalloproteinase inhibition: implications for reversibility of liver fibrosis. J Biol Chem 2002;277:11069-11076. https://doi.org/10.1074/jbc.M111490200
- Iredale J. Defining therapeutic targets for liver fibrosis: exploiting the biology of inflammation and repair. Pharmacol Res 2008;58:129-136. https://doi.org/10.1016/j.phrs.2008.06.011
- Iredale JP, Benyon RC, Arthur MJ, et al. Tissue inhibitor of metalloproteinase-1 messenger RNA expression is enhanced relative to interstitial collagenase messenger RNA in experimental liver injury and fibrosis. Hepatology 1996;24:176-184. https://doi.org/10.1002/hep.510240129
- Issa R, Zhou X, Constandinou CM, et al. Spontaneous recovery from micronodular cirrhosis: evidence for incomplete resolution associated with matrix cross-linking. Gastroenterology 2004;126:1795-1808. https://doi.org/10.1053/j.gastro.2004.03.009
- Parsons CJ, Bradford BU, Pan CQ, et al. Antifibrotic effects of a tissue inhibitor of metalloproteinase-1 antibody on established liver fibrosis in rats. Hepatology 2004;40:1106-1115. https://doi.org/10.1002/hep.20425
- Fallowfield JA, Mizuno M, Kendall TJ, et al. Scar-associated macrophages are a major source of hepatic matrix metalloproteinase-13 and facilitate the resolution of murine hepatic fibrosis. J Immunol 2007;178:5288-5295. https://doi.org/10.4049/jimmunol.178.8.5288
- Pellicoro A, Aucott RL, Ramachandran P, et al. Elastin accumulation is regulated at the level of degradation by macrophage metalloelastase (MMP-12) during experimental liver fibrosis. Hepatology 2012;55:1965-1975. https://doi.org/10.1002/hep.25567
- Tacke F, Zimmermann HW. Macrophage heterogeneity in liver injury and fibrosis. J Hepatol 2014;60:1090-1096.
- Jiao J, Sastre D, Fiel MI, et al. Dendritic cell regulation of carbon tetrachloride-induced murine liver fibrosis regression. Hepatology 2012;55:244-255. https://doi.org/10.1002/hep.24621
- Mallat A, Lotersztajn S. Reversion of hepatic stellate cell to a quiescent phenotype: from myth to reality? J Hepatol 2013;59:383-386. https://doi.org/10.1016/j.jhep.2013.03.031
- Troeger JS, Mederacke I, Gwak GY, et al. Deactivation of hepatic stellate cells during liver fibrosis resolution in mice. Gastroenterology 2012;143:1073-1083. https://doi.org/10.1053/j.gastro.2012.06.036
- Kisseleva T, Cong M, Paik Y, et al. Myofibroblasts revert to an inactive phenotype during regression of liver fibrosis. Proc Natl Acad Sci U S A 2012;109:9448-9453. https://doi.org/10.1073/pnas.1201840109
- Pellicoro A, Ramachandran P, Iredale JP, Fallowfield JA. Liver fibrosis and repair: immune regulation of wound healing in a solid organ. Nat Rev Immunol 2014;14:181-194. https://doi.org/10.1038/nri3623
- Ellis EL, Mann DA. Clinical evidence for the regression of liver fibrosis. J Hepatol 2012;56:1171-1180. https://doi.org/10.1016/j.jhep.2011.09.024
- van Zonneveld M, Zondervan PE, Cakaloglu Y, et al. Peg-interferon improves liver histology in patients with HBeAg-positive chronic hepatitis B: no additional benefit of combination with lamivudine. Liver Int 2006;26:399-405. https://doi.org/10.1111/j.1478-3231.2006.01257.x
- Dienstag JL, Goldin RD, Heathcote EJ, et al. Histological outcome during long-term lamivudine therapy. Gastroenterology 2003;124:105-117. https://doi.org/10.1053/gast.2003.50013
- Chang TT, Liaw YF, Wu SS, et al. Long-term entecavir therapy results in the reversal of fibrosis/cirrhosis and continued histological improvement in patients with chronic hepatitis B. Hepatology 2010;52:886-893. https://doi.org/10.1002/hep.23785
- Marcellin P, Gane E, Buti M, et al. Regression of cirrhosis during treatment with tenofovir disoproxil fumarate for chronic hepatitis B: a 5-year open-label follow-up study. Lancet 2013;381:468-475. https://doi.org/10.1016/S0140-6736(12)61425-1
- George SL, Bacon BR, Brunt EM, Mihindukulasuriya KL, Hoffmann J, Di Bisceglie AM. Clinical, virologic, histologic, and biochemical outcomes after successful HCV therapy: a 5-year follow-up of 150 patients. Hepatology 2009;49:729-738. https://doi.org/10.1002/hep.22694
- Verrill C, Markham H, Templeton A, Carr NJ, Sheron N. Alcohol-related cirrhosis: early abstinence is a key factor in prognosis, even in the most severe cases. Addiction 2009;104:768-774. https://doi.org/10.1111/j.1360-0443.2009.02521.x
- Sanyal AJ, Chalasani N, Kowdley KV, et al. Pioglitazone, vitamin E, or placebo for nonalcoholic steatohepatitis. N Engl J Med 2010;362:1675-1685. https://doi.org/10.1056/NEJMoa0907929
- Czaja AJ, Carpenter HA. Decreased fibrosis during corticosteroid therapy of autoimmune hepatitis. J Hepatol 2004;40:646-652.
- Mohamadnejad M, Malekzadeh R, Nasseri-Moghaddam S, et al. Impact of immunosuppressive treatment on liver fibrosis in autoimmune hepatitis. Dig Dis Sci 2005;50:547-551. https://doi.org/10.1007/s10620-005-2472-5
- Colmenero J, Bataller R, Sancho-Bru P, et al. Effects of losartan on hepatic expression of nonphagocytic NADPH oxidase and fibrogenic genes in patients with chronic hepatitis C. Am J Physiol Gastrointest Liver Physiol 2009;297:G726-G734. https://doi.org/10.1152/ajpgi.00162.2009
- McHutchison J, Goodman Z, Patel K, et al. Farglitazar lacks antifibrotic activity in patients with chronic hepatitis C infection. Gastroenterology 2010;138:1365-1373. https://doi.org/10.1053/j.gastro.2009.12.003
- Kim MY, Cho MY, Baik SK, et al. Beneficial effects of candesartan, an angiotensin-blocking agent, on compensated alcoholic liver fibrosis: a randomized open-label controlled study. Liver Int 2012;32:977-987. https://doi.org/10.1111/j.1478-3231.2012.02774.x
- Aithal GP, Thomas JA, Kaye PV, et al. Randomized, placebo-controlled trial of pioglitazone in nondiabetic subjects with nonalcoholic steatohepatitis. Gastroenterology 2008;135:1176-1184. https://doi.org/10.1053/j.gastro.2008.06.047
- Ratziu V, Charlotte F, Bernhardt C, et al. Long-term efficacy of rosiglitazone in nonalcoholic steatohepatitis: results of the fatty liver improvement by rosiglitazone therapy (FLIRT 2) extension trial. Hepatology 2010;51:445-453. https://doi.org/10.1002/hep.23270
- Zein CO, Yerian LM, Gogate P, et al. Pentoxifylline improves nonalcoholic steatohepatitis: a randomized placebo-controlled trial. Hepatology 2011;54:1610-1619. https://doi.org/10.1002/hep.24544
- Ratziu V, de Ledinghen V, Oberti F, et al. A randomized controlled trial of high-dose ursodesoxycholic acid for nonalcoholic steatohepatitis. J Hepatol 2011;54:1011-1019. https://doi.org/10.1016/j.jhep.2010.08.030
- Neuschwander-Tetri BA, Loomba R, Sanyal AJ, et al. Farnesoid X nuclear receptor ligand obeticholic acid for non-cirrhotic, non-alcoholic steatohepatitis (FLINT): a multicentre, randomised, placebo-controlled trial. Lancet 2015;385:956-965. https://doi.org/10.1016/S0140-6736(14)61933-4
- Poupon RE, Poupon R, Balkau B. Ursodiol for the longterm treatment of primary biliary cirrhosis: the UDCA-PBC Study Group. N Engl J Med 1994;330:1342-1327. https://doi.org/10.1056/NEJM199405123301903
- Corpechot C, Carrat F, Bonnand AM, Poupon RE, Poupon R. The effect of ursodeoxycholic acid therapy on liver fibrosis progression in primary biliary cirrhosis. Hepatology 2000;32:1196-1199. https://doi.org/10.1053/jhep.2000.20240
- Korean Association for the Study of the Liver. KASL clinical practice guidelines: management of chronic hepatitis B. Clin Mol Hepatol 2016;22:18-75. https://doi.org/10.3350/cmh.2016.22.1.18
- Liaw YF. Reversal of cirrhosis: an achievable goal of hepatitis B antiviral therapy. J Hepatol 2013;59:880-881. https://doi.org/10.1016/j.jhep.2013.05.007
- Papatheodoridis GV, Petraki K, Cholongitas E, Kanta E, Ketikoglou I, Manesis EK. Impact of interferon-alpha therapy on liver fibrosis progression in patients with HBeAg-negative chronic hepatitis B. J Viral Hepat 2005;12:199-206. https://doi.org/10.1111/j.1365-2893.2005.00582.x
- Chang XM, Chang Y, Jia A. Effects of interferon-alpha on expression of hepatic stellate cell and transforming growth factor-beta1 and alpha-smooth muscle actin in rats with hepatic fibrosis. World J Gastroenterol 2005;11:2634-2636. https://doi.org/10.3748/wjg.v11.i17.2634
- Weng H, Mertens PR, Gressner AM, Dooley S. IFN-gamma abrogates profibrogenic TGF-beta signaling in liver by targeting expression of inhibitory and receptor Smads. J Hepatol 2007;46:295-303.
- Fung J, Lai CL, Wong DK, Seto WK, Hung I, Yuen MF. Significant changes in liver stiffness measurements in patients with chronic hepatitis B: 3-year follow-up study. J Viral Hepat 2011;18:e200-e205. https://doi.org/10.1111/j.1365-2893.2010.01428.x
- Kim SU, Park JY, Kim DY, et al. Non-invasive assessment of changes in liver fibrosis via liver stiffness measurement in patients with chronic hepatitis B: impact of antiviral treatment on fibrosis regression. Hepatol Int 2010;4:673-680. https://doi.org/10.1007/s12072-010-9201-7
- Shin SK, Kim JH, Park H, et al. Improvement of liver function and non-invasive fibrosis markers in hepatitis B virus-associated cirrhosis: 2 years of entecavir treatment. J Gastroenterol Hepatol 2015;30:1775-1781. https://doi.org/10.1111/jgh.13020
- Yo IK, Kwon OS, Park JW, et al. The factors associated with longitudinal changes in liver stiffness in patients with chronic hepatitis B. Clin Mol Hepatol 2015;21:32-40. https://doi.org/10.3350/cmh.2015.21.1.32
- Everson GT. Management of cirrhosis due to chronic hepatitis C. J Hepatol 2005;42 Suppl:S65-S74. https://doi.org/10.1016/j.jhep.2005.01.009
- Veldt BJ, Heathcote EJ, Wedemeyer H, et al. Sustained virologic response and clinical outcomes in patients with chronic hepatitis C and advanced fibrosis. Ann Intern Med 2007;147:677-684. https://doi.org/10.7326/0003-4819-147-10-200711200-00003
- Bachofner JA, Valli PV, Kroger A, et al. Direct antiviral agent treatment of chronic hepatitis C results in rapid regression of transient elastography and fibrosis markers fibrosis-4 score and aspartate aminotransferase-platelet ratio index. Liver Int 2016 Sep 28 [Epub]. http://doi.org/10.1111/liv.13256.
- Rambaldi A, Gluud C. Colchicine for alcoholic and non-alcoholic liver fibrosis and cirrhosis. Cochrane Database Syst Rev 2005;(2):CD002148.
- Musso G, Gambino R, Cassader M, Pagano G. A meta-analysis of randomized trials for the treatment of nonalcoholic fatty liver disease. Hepatology 2010;52:79-104.
- Promrat K, Kleiner DE, Niemeier HM, et al. Randomized controlled trial testing the effects of weight loss on nonalcoholic steatohepatitis. Hepatology 2010;51:121-129. https://doi.org/10.1002/hep.23276
- Neuschwander-Tetri BA. Targeting the FXR nuclear receptor to treat liver disease. Gastroenterology 2015;148:704-706. https://doi.org/10.1053/j.gastro.2015.02.037
- Roberts SK, Therneau TM, Czaja AJ. Prognosis of histological cirrhosis in type 1 autoimmune hepatitis. Gastroenterology 1996;110:848-857. https://doi.org/10.1053/gast.1996.v110.pm8608895
- Czaja AJ, Manns MP. Advances in the diagnosis, pathogenesis, and management of autoimmune hepatitis. Gastroenterology 2010;139:58-72. https://doi.org/10.1053/j.gastro.2010.04.053
- Czaja AJ. Review article: the prevention and reversal of hepatic fibrosis in autoimmune hepatitis. Aliment Pharmacol Ther 2014;39:385-406. https://doi.org/10.1111/apt.12592
- Karlsen TH, Vesterhus M, Boberg KM. Review article: controversies in the management of primary biliary cirrhosis and primary sclerosing cholangitis. Aliment Pharmacol Ther 2014;39:282-301. https://doi.org/10.1111/apt.12581
- Lindor KD, Gershwin ME, Poupon R, et al. Primary biliary cirrhosis. Hepatology 2009;50:291-308. https://doi.org/10.1002/hep.22906
- Goulis J, Leandro G, Burroughs AK. Randomised controlled trials of ursodeoxycholic-acid therapy for primary biliary cirrhosis: a meta-analysis. Lancet 1999;354:1053-1060. https://doi.org/10.1016/S0140-6736(98)11293-X
- Gong Y, Huang ZB, Christensen E, Gluud C. Ursodeoxycholic acid for primary biliary cirrhosis. Cochrane Database Syst Rev 2008;(3):CD000551.
- Prince MI, Chetwynd A, Craig WL, Metcalf JV, James OF. Asymptomatic primary biliary cirrhosis: clinical features, prognosis, and symptom progression in a large population based cohort. Gut 2004;53:865-870. https://doi.org/10.1136/gut.2003.023937
- Kaplan MM, Cheng S, Price LL, Bonis PA. A randomized controlled trial of colchicine plus ursodiol versus methotrexate plus ursodiol in primary biliary cirrhosis: ten-year results. Hepatology 2004;39:915-923. https://doi.org/10.1002/hep.20103
- Corpechot C. Primary biliary cirrhosis and bile acids. Clin Res Hepatol Gastroenterol 2012;36 Suppl 1:S13-S20. https://doi.org/10.1016/S2210-7401(12)70016-5
- Hirschfield GM, Mason A, Luketic V, et al. Efficacy of obeticholic acid in patients with primary biliary cirrhosis and inadequate response to ursodeoxycholic acid. Gastroenterology 2015;148:751-761. https://doi.org/10.1053/j.gastro.2014.12.005
- Bacon BR, Adams PC, Kowdley KV, Powell LW, Tavill AS; American Association for the Study of Liver Diseases. Diagnosis and management of hemochromatosis: 2011 practice guideline by the American Association for the Study of Liver Diseases. Hepatology 2011;54:328-343.
- Falize L, Guillygomarc'h A, Perrin M, et al. Reversibility of hepatic fibrosis in treated genetic hemochromatosis: a study of 36 cases. Hepatology 2006;44:472-477. https://doi.org/10.1002/hep.21260
- Mehal WZ, Schuppan D. Antifibrotic therapies in the liver. Semin Liver Dis 2015;35:184-198. https://doi.org/10.1055/s-0035-1550055
- Patsenker E, Popov Y, Stickel F, Jonczyk A, Goodman SL, Schuppan D. Inhibition of integrin alphavbeta6 on cholangiocytes blocks transforming growth factor-beta activation and retards biliary fibrosis progression. Gastroenterology 2008;135:660-670. https://doi.org/10.1053/j.gastro.2008.04.009
-
Wang Q, Usinger W, Nichols B, et al. Cooperative interaction of CTGF and TGF-
$\beta$ in animal models of fibrotic disease. Fibrogenesis Tissue Repair 2011;4:4. https://doi.org/10.1186/1755-1536-4-4 - Giannone FA, Baldassarre M, Domenicali M, et al. Reversal of liver fibrosis by the antagonism of endocannabinoid CB1 receptor in a rat model of CCl(4)-induced advanced cirrhosis. Lab Invest 2012;92:384-395. https://doi.org/10.1038/labinvest.2011.191
- Jiang JX, Chen X, Serizawa N, et al. Liver fibrosis and hepatocyte apoptosis are attenuated by GKT137831, a novel NOX4/NOX1 inhibitor in vivo. Free Radic Biol Med 2012;53:289-296. https://doi.org/10.1016/j.freeradbiomed.2012.05.007
- Staels B, Rubenstrunk A, Noel B, et al. Hepatoprotective effects of the dual peroxisome proliferator-activated receptor alpha/delta agonist, GFT505, in rodent models of nonalcoholic fatty liver disease/nonalcoholic steatohepatitis. Hepatology 2013;58:1941-1952. https://doi.org/10.1002/hep.26461
- Safadi R, Konikoff FM, Mahamid M, et al. The fatty acid-bile acid conjugate Aramchol reduces liver fat content in patients with nonalcoholic fatty liver disease. Clin Gastroenterol Hepatol 2014;12:2085-2091. https://doi.org/10.1016/j.cgh.2014.04.038
- Gonzalez EO, Boix V, Deltoro MG, et al. The effects of Maraviroc on liver fibrosis in HIV/HCV co-infected patients. J Int AIDS Soc 2014;17(4 Suppl 3):19643. https://doi.org/10.7448/IAS.17.4.19643
- Yang JJ, Tao H, Li J. Hedgehog signaling pathway as key player in liver fibrosis: new insights and perspectives. Expert Opin Ther Targets 2014;18:1011-1021. https://doi.org/10.1517/14728222.2014.927443
-
Samarakoon R, Overstreet JM, Higgins PJ. TGF-
$\beta$ signaling in tissue fibrosis: redox controls, target genes and therapeutic opportunities. Cell Signal 2013;25:264-268. https://doi.org/10.1016/j.cellsig.2012.10.003 - Tam J, Cinar R, Liu J, et al. Peripheral cannabinoid-1 receptor inverse agonism reduces obesity by reversing leptin resistance. Cell Metab 2012;16:167-179. https://doi.org/10.1016/j.cmet.2012.07.002
-
Baghdasaryan A, Claudel T, Gumhold J, et al. Dual farnesoid X receptor/TGR5 agonist INT-767 reduces liver injury in the Mdr2-/- (Abcb4-/-) mouse cholangiopathy model by promoting biliary
$HCO^-_3$ output. Hepatology 2011;54:1303-1312. https://doi.org/10.1002/hep.24537 - Eom YW, Shim KY, Baik SK. Mesenchymal stem cell therapy for liver fibrosis. Korean J Intern Med 2015;30:580-589. https://doi.org/10.3904/kjim.2015.30.5.580
Cited by
- Clinical and Pathological Risk Factors Associated with Liver Fibrosis and Steatosis in African-Americans with Chronic Hepatitis C vol.62, pp.8, 2017, https://doi.org/10.1007/s10620-017-4626-7
- Transient Elastography (FibroScan) Performs Better Than Non-Invasive Markers in Assessing Liver Fibrosis and Cirrhosis in Autoimmune Hepatitis Patients vol.23, pp.None, 2017, https://doi.org/10.12659/msm.907300
- Metabolomic profiling for identification of metabolites and relevant pathways for taurine in hepatic stellate cells vol.23, pp.31, 2017, https://doi.org/10.3748/wjg.v23.i31.5713
- Fagonia indica Repairs Hepatic Damage through Expression Regulation of Toll-Like Receptors in a Liver Injury Model vol.2018, pp.None, 2017, https://doi.org/10.1155/2018/7967135
- Comparative evaluation of GPR versus APRI and FIB‐4 in predicting different levels of liver fibrosis of chronic hepatitis B vol.25, pp.5, 2018, https://doi.org/10.1111/jvh.12842
- New Concepts on Reversibility and Targeting of Liver Fibrosis; A Review Article vol.10, pp.3, 2018, https://doi.org/10.15171/mejdd.2018.103
- Transcriptional Regulatory Networks in Hepatitis C Virus-induced Hepatocellular Carcinoma vol.8, pp.None, 2017, https://doi.org/10.1038/s41598-018-32464-5
- Chemically modified liposomes carrying TRAIL target activated hepatic stellate cells and ameliorate hepatic fibrosis in vitro and in vivo vol.23, pp.3, 2017, https://doi.org/10.1111/jcmm.14097
- Polycomb Repressive Complex 2 Proteins EZH1 and EZH2 Regulate Timing of Postnatal Hepatocyte Maturation and Fibrosis by Repressing Genes With Euchromatic Promoters in Mice vol.156, pp.6, 2019, https://doi.org/10.1053/j.gastro.2019.01.041
- Early detection and staging of chronic liver diseases with a protein MRI contrast agent vol.10, pp.1, 2017, https://doi.org/10.1038/s41467-019-11984-2
- MRI as an alternative to serum ferritin for diagnosis of iron overload in children in the context of immune response after stem cell transplantation vol.23, pp.8, 2017, https://doi.org/10.1111/petr.13583
- The effect of vitamin D supplementation on the progression of fibrosis in patients with chronic liver disease : A protocol for a systematic review and meta-analysis vol.99, pp.19, 2020, https://doi.org/10.1097/md.0000000000020296
- Recompensation of Decompensated Hepatitis B Cirrhosis: Current Status and Challenges vol.2020, pp.None, 2017, https://doi.org/10.1155/2020/9609731
- Origin and role of hepatic myofibroblasts in hepatocellular carcinoma vol.11, pp.13, 2020, https://doi.org/10.18632/oncotarget.27532
- Decellularized liver matrix as substrates for rescue of acute hepatocytes toxicity vol.108, pp.4, 2017, https://doi.org/10.1002/jbm.b.34506
- Immunomodulatory effect of curcumin on hepatic cirrhosis in experimental rats vol.44, pp.6, 2017, https://doi.org/10.1111/jfbc.13219
- Ultrasound-based liver elastography in the assessment of fibrosis vol.75, pp.11, 2020, https://doi.org/10.1016/j.crad.2020.01.005
- Quantitative HBcrAg and HBcAb versus HBsAg and HBV DNA in predicting liver fibrosis levels of chronic hepatitis B patients vol.43, pp.9, 2017, https://doi.org/10.1016/j.gastre.2020.03.005
- Quantitative HBcrAg and HBcAb versus HBsAg and HBV DNA in predicting liver fibrosis levels of chronic hepatitis B patients vol.43, pp.9, 2020, https://doi.org/10.1016/j.gastrohep.2020.03.017
- The Role of the Gut Microbiome in Liver Cirrhosis Treatment vol.22, pp.1, 2021, https://doi.org/10.3390/ijms22010199
- Research Trends in the Efficacy of Stem Cell Therapy for Hepatic Diseases Based on MicroRNA Profiling vol.22, pp.1, 2021, https://doi.org/10.3390/ijms22010239
- Use of Texture Analysis on Noncontrast MRI in Classification of Early Stage of Liver Fibrosis vol.2021, pp.None, 2017, https://doi.org/10.1155/2021/6677821
- Molecular factors associated with regression of liver fibrosis of alcoholic etiology vol.93, pp.2, 2021, https://doi.org/10.26442/00403660.2021.02.200617
- The Gut Microbiota-Derived Immune Response in Chronic Liver Disease vol.22, pp.15, 2021, https://doi.org/10.3390/ijms22158309
- Cellular and Molecular Mechanisms Underlying Liver Fibrosis Regression vol.10, pp.10, 2017, https://doi.org/10.3390/cells10102759
- Cyclic GMP in Liver Cirrhosis-Role in Pathophysiology of Portal Hypertension and Therapeutic Implications vol.22, pp.19, 2017, https://doi.org/10.3390/ijms221910372
- Hepatocellular carcinoma risk after viral response in hepatitis C virus-advanced fibrosis: Who to screen and for how long? vol.27, pp.40, 2017, https://doi.org/10.3748/wjg.v27.i40.6737
- Hepatotoxicity or hepatoprotection of emodin? Two sides of the same coin by 1H-NMR metabolomics profiling vol.431, pp.None, 2017, https://doi.org/10.1016/j.taap.2021.115734
- The Gut-Liver Axis in Chronic Liver Disease: A Macrophage Perspective vol.10, pp.11, 2017, https://doi.org/10.3390/cells10112959
- Preventive and therapeutic role of betaine in liver disease: A review on molecular mechanisms vol.912, pp.None, 2021, https://doi.org/10.1016/j.ejphar.2021.174604
- Hepatic Stellate Cell: A Double-Edged Sword in the Liver vol.6, pp.None, 2017, https://doi.org/10.33549/physiolres.934755