Emerging therapies for liver fibrosis

被引:60
作者
Fowell, Andrew J.
Iredale, John P. [1 ]
机构
[1] Univ Edinburgh, Ctr Inflammat Res, MRC, Edinburgh ED16 4TJ, Midlothian, Scotland
[2] Univ Southampton, Southampton Gen Hosp, Div Infect Inflammat & Repair, Liver Res Grp, Southampton SO9 5NH, Hants, England
关键词
cirrhosis; antifibrotic therapy; hepatic stellate cell; matrix degradation; apoptosis;
D O I
10.1159/000090320
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Liver fibrosis occurs as a result of a wide range of injurious processes and in its end-stage results in cirrhosis. This gross disruption of liver architecture is associated with impaired hepatic function, portal hypertension and significant resultant morbidity and mortality. Indeed, liver fibrosis and cirrhosis represent a major worldwide healthcare burden. Recent progress in liver transplantation, the management of portal hypertension and the treatment of chronic viral hepatitis have had an important impact. However, these approaches are not without their limitations-in particular, issues regarding organ availability for transplantation-and serve to highlight the urgent requirement to influence pharmacologically the underlying fibrotic process in many patients. Liver fibrosis has been shown to be a bidirectional process and increasing data from laboratory and clinical studies reveal that even advanced fibrosis and cirrhosis are potentially reversible. Exploration of the molecular mechanisms underlying this bi-directionality will lead to characterisation of the essential attributes of an antifibrotic therapy. In this review, these mechanisms are highlighted and the growing number of emerging antifibrotic agents discussed. Copyright (c) 2006 S. Karger AG, Basel.
引用
收藏
页码:174 / 183
页数:10
相关论文
共 75 条
[1]
Adenoviral-mediated transfer of p53 or retinoblastoma protein blocks cell proliferation and induces apoptosis in culture-activated hepatic stellate cells [J].
Abriss, B ;
Hollweg, G ;
Gressner, AM ;
Weiskirchen, R .
JOURNAL OF HEPATOLOGY, 2003, 38 (02) :169-178
[2]
[Anonymous], 2001, ANN REP CHIEF MED OF
[3]
Adenoviral expression of a transforming growth factor-β1 antisense mRNA is effective in preventing liver fibrosis in bile-duct ligated rats -: art. no. 29 [J].
Arias, M ;
Sauer-Lehnen, S ;
Treptau, J ;
Janoschek, N ;
Theuerkauf, I ;
Buettner, R ;
Gressner, AM ;
Weiskirchen, R .
BMC GASTROENTEROLOGY, 2003, 3 (1)
[4]
Baroni GS, 1996, HEPATOLOGY, V23, P1189
[5]
Successful targeting to rat hepatic stellate cells using albumin modified with cyclic peptides that recognize the collagen type VI receptor [J].
Beljaars, L ;
Molema, G ;
Schuppan, D ;
Geerts, A ;
De Bleser, PJ ;
Weert, B ;
Meijer, DKF ;
Poelstra, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (17) :12743-12751
[6]
Albumin modified with mannose 6-phosphate: A potential carrier for selective delivery of antifibrotic drugs to rat and human hepatic stellate cells [J].
Beljaars, L ;
Molema, G ;
Weert, B ;
Bonnema, H ;
Olinga, P ;
Groothuis, GMM ;
Meijer, DKF ;
Poelstra, K .
HEPATOLOGY, 1999, 29 (05) :1486-1493
[7]
Extracellular matrix degradation and the role of hepatic stellate cells [J].
Benyon, RC ;
Arthur, MJP .
SEMINARS IN LIVER DISEASE, 2001, 21 (03) :373-384
[8]
Analysis of Arg-Gly-Asp mimetics and soluble receptor of tumour necrosis factor as therapeutic modalities for concanavalin A induced hepatitis in mice [J].
Bruck, R ;
Shirin, H ;
Hershkoviz, R ;
Lider, O ;
Kenet, G ;
Aeed, H ;
Matas, Z ;
Zaidel, L ;
Halpern, Z .
GUT, 1997, 40 (01) :133-138
[9]
Efficacy and safety of imatinib mesylate in advanced gastrointestinal stromal tumors [J].
Demetri, GD ;
von Mehren, M ;
Blanke, CD ;
Van den Abbeele, AD ;
Eisenberg, B ;
Roberts, PJ ;
Heinrich, MC ;
Tuveson, DA ;
Singer, S ;
Janicek, M ;
Fletcher, JA ;
Silverman, SG ;
Silberman, SL ;
Capdeville, R ;
Kiese, B ;
Peng, B ;
Dimitrijevic, S ;
Druker, BJ ;
Corless, C ;
Fletcher, CDM ;
Joensuu, H .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (07) :472-480
[10]
Selective Na+/H+ exchange inhibition by cariporide reduces liver fibrosis in the rat [J].
Di Sario, A ;
Bendia, E ;
Taffetani, S ;
Marzioni, M ;
Candelaresi, C ;
Pigini, P ;
Schindler, U ;
Kleemann, HW ;
Trozzi, L ;
Macarri, G ;
Benedetti, A .
HEPATOLOGY, 2003, 37 (02) :256-266