Literature DB >> 12530948

Treatment of hepatic fibrosis: almost there.

Efsevia Albanis1, Rifaat Safadi, Scott L Friedman.   

Abstract

Hepatic fibrosis is the scarring response of the liver to chronic liver injury; when fibrosis progresses to cirrhosis, morbid complications can develop. Available therapies for many chronic liver diseases are ineffective, with liver transplantation as the only option, though the supply of donor organs is inadequate to meet the growing demand. Novel approaches that attack the scarring response are therefore urgently needed. Optimism in this effort is fueled by major insights into the pathogenesis of fibrosis and by accumulating evidence that even cirrhosis is reversible in many patients. Most evolving antifibrotic therapies will be aimed at inhibiting the activated hepatic stellate cell, which is responsible for the fibrotic response to injury. This review describes the ways in which insights into the cellular basis of hepatic fibrosis are leading to realistic strategies for antifibrotic treatment that may revolutionize the management of patients with chronic liver disease.

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Year:  2003        PMID: 12530948     DOI: 10.1007/s11894-003-0009-7

Source DB:  PubMed          Journal:  Curr Gastroenterol Rep        ISSN: 1522-8037


  50 in total

1.  Is liver fibrosis reversible?

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Journal:  N Engl J Med       Date:  2001-02-08       Impact factor: 91.245

2.  Monocyte chemotactic protein-1 as a chemoattractant for human hepatic stellate cells.

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Journal:  Hepatology       Date:  1999-01       Impact factor: 17.425

3.  Excess iron induces hepatic oxidative stress and transforming growth factor beta1 in genetic hemochromatosis.

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Journal:  Hepatology       Date:  1997-09       Impact factor: 17.425

4.  Prevention of rat hepatic fibrosis by the protease inhibitor, camostat mesilate, via reduced generation of active TGF-beta.

Authors:  M Okuno; K Akita; H Moriwaki; N Kawada; K Ikeda; K Kaneda; Y Suzuki; S Kojima
Journal:  Gastroenterology       Date:  2001-06       Impact factor: 22.682

5.  A selective ROCK inhibitor, Y27632, prevents dimethylnitrosamine-induced hepatic fibrosis in rats.

Authors:  S Tada; H Iwamoto; M Nakamuta; R Sugimoto; M Enjoji; Y Nakashima; H Nawata
Journal:  J Hepatol       Date:  2001-04       Impact factor: 25.083

6.  Liver cirrhosis is reverted by urokinase-type plasminogen activator gene therapy.

Authors:  S Salgado; J Garcia; J Vera; F Siller; M Bueno; A Miranda; A Segura; G Grijalva; J Segura; H Orozco; R Hernandez-Pando; M Fafutis; L K Aguilar; E Aguilar-Cordova; J Armendariz-Borunda
Journal:  Mol Ther       Date:  2000-12       Impact factor: 11.454

7.  Endothelin antagonism in experimental hepatic fibrosis. Implications for endothelin in the pathogenesis of wound healing.

Authors:  D C Rockey; J J Chung
Journal:  J Clin Invest       Date:  1996-09-15       Impact factor: 14.808

8.  Mechanisms of spontaneous resolution of rat liver fibrosis. Hepatic stellate cell apoptosis and reduced hepatic expression of metalloproteinase inhibitors.

Authors:  J P Iredale; R C Benyon; J Pickering; M McCullen; M Northrop; S Pawley; C Hovell; M J Arthur
Journal:  J Clin Invest       Date:  1998-08-01       Impact factor: 14.808

9.  Effects and regulation of connective tissue growth factor on hepatic stellate cells.

Authors:  Valerie Paradis; Delphine Dargere; Franck Bonvoust; Michel Vidaud; Patricia Segarini; Pierre Bedossa
Journal:  Lab Invest       Date:  2002-06       Impact factor: 5.662

10.  Leptin enhances wound re-epithelialization and constitutes a direct function of leptin in skin repair.

Authors:  S Frank; B Stallmeyer; H Kämpfer; N Kolb; J Pfeilschifter
Journal:  J Clin Invest       Date:  2000-08       Impact factor: 14.808

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  8 in total

Review 1.  Gene modulation for treating liver fibrosis.

Authors:  Kun Cheng; Ram I Mahato
Journal:  Crit Rev Ther Drug Carrier Syst       Date:  2007       Impact factor: 4.889

2.  Relationship between clinical and pathologic findings in patients with chronic liver diseases.

Authors:  Lun-Gen Lu; Min-De Zeng; Yi-Min Mao; Ji-Qiang Li; De-Kai Qiu; Jing-Yuan Fang; Ai-Ping Cao; Mo-Bin Wan; Cheng-Zhong Li; Jun Ye; Xiong Cai; Cheng-Wei Chen; Ji-Yao Wang; Shan-Ming Wu; Jin-Shui Zhu; Xia-Qiu Zhou
Journal:  World J Gastroenterol       Date:  2003-12       Impact factor: 5.742

3.  Dynamic changes of capillarization and peri-sinusoid fibrosis in alcoholic liver diseases.

Authors:  Guang-Fu Xu; Xin-Yue Wang; Gui-Ling Ge; Peng-Tao Li; Xu Jia; De-Lu Tian; Liang-Duo Jiang; Jin-Xiang Yang
Journal:  World J Gastroenterol       Date:  2004-01-15       Impact factor: 5.742

4.  Effect of interferon alpha and ribavirin treatment on serum levels of transforming growth factor-beta1, vascular endothelial growth factor, and basic fibroblast growth factor in patients with chronic hepatitis C.

Authors:  Ewa Janczewska-Kazek; Bogdan Marek; Dariusz Kajdaniuk; Halina Borgiel-Marek
Journal:  World J Gastroenterol       Date:  2006-02-14       Impact factor: 5.742

5.  Anti-inflammatory/anti-fibrotic effects of the hepatoprotective silymarin and the schistosomicide praziquantel against Schistosoma mansoni-induced liver fibrosis.

Authors:  Naglaa M El-Lakkany; Olfat A Hammam; Walaa H El-Maadawy; Afkar A Badawy; Afaf A Ain-Shoka; Fatma A Ebeid
Journal:  Parasit Vectors       Date:  2012-01-11       Impact factor: 3.876

6.  Th17 down-regulation is involved in reduced progression of schistosomiasis fibrosis in ICOSL KO mice.

Authors:  Bo Wang; Song Liang; Yu Wang; Xing-Quan Zhu; Wei Gong; Hui-Qin Zhang; Ying Li; Chao-Ming Xia
Journal:  PLoS Negl Trop Dis       Date:  2015-01-15

7.  Inhibition of collagen fibril formation.

Authors:  Andrzej Steplewski; Andrzej Fertala
Journal:  Fibrogenesis Tissue Repair       Date:  2012-06-06

8.  Complementary Effect of Capparis Spinosa L. and Silymarin With/without Praziquantel on Mice Experimentally Infected with Schistosoma Mansoni.

Authors:  S S El-Hawary; K F Taha; F N Kirillos; A A Dahab; A A El-Mahis; S H El-Sayed
Journal:  Helminthologia       Date:  2018-01-27       Impact factor: 1.184

  8 in total

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