Title of article :
New Concepts on Reversibility and Targeting of Liver Fibrosis; A Review Article
Author/Authors :
Ebrahimi, Hedyeh The Liver - Pancreatic and Biliary Diseases Research Center - Digestive Disease Research Institute - Shariati Hospital - Tehran University of Medical Sciences, Tehran - Non-Communicable Diseases Research Center - Endocrinology and Metabolism Population Sciences Institute - Tehran University of Medical Sciences, Tehran , Naderian, Mohammadreza The Liver - Pancreatic and Biliary Diseases Research Center - Digestive Disease Research Institute - Shariati Hospital - Tehran University of Medical Sciences, Tehran - Non-Communicable Diseases Research Center - Endocrinology and Metabolism Population Sciences Institute - Tehran University of Medical Sciences, Tehran , Sohrabpour, Amir Ali The Liver - Pancreatic and Biliary Diseases Research Center - Digestive Disease Research Institute - Shariati Hospital - Tehran University of Medical Sciences, Tehran
Pages :
16
From page :
133
To page :
148
Abstract :
Currently, liver fibrosis and its complications are regarded as critical health problems. With the studies showing the reversible nature of liver fibrogenesis, scientists have focused on understanding the underlying mechanism of this condition in order to develop new therapeutic strategies. Although hepatic stellate cells are known as the primary cells responsible for liver fibrogenesis, studies have shown contributing roles for other cells, pathways, and molecules in the development of fibrosis depending on the etiology of liver fibrosis. Hence, interventions could be directed in the proper way for each type of liver diseases to better address this complication. There are two main approaches in clinical reversion of liver fibrosis; eliminating the underlying insult and targeting the fibrosis process, which have variable clinical importance in the treatment of this disease. In this review, we present recent concepts in molecular pathways of liver fibrosis reversibility and their clinical implications.
Keywords :
Fibrosis , Genetic therapy , Liver cirrhosis , Therapeutics , Gene targeting
Journal title :
Astroparticle Physics
Serial Year :
2018
Record number :
2417536
Link To Document :
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