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Published in: Journal of Translational Medicine 1/2022

Open Access 01-12-2022 | Idiopathic Pulmonary Fibrosis | Review

Targeting HSP47 and HSP70: promising therapeutic approaches in liver fibrosis management

Authors: Eslam E. Abd El-Fattah, Amr Y. Zakaria

Published in: Journal of Translational Medicine | Issue 1/2022

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Abstract

Liver fibrosis is a liver disease in which there is an excessive buildup of extracellular matrix proteins, including collagen. By regulating cytokine production and the inflammatory response, heat shock proteins (HSPs) contribute significantly to a wider spectrum of fibrotic illnesses, such as lung, liver, and idiopathic pulmonary fibrosis by aiding in the folding and assembly of freshly synthesized proteins, HSPs serve as chaperones. HSP70 is one of the key HSPs in avoiding protein aggregation which induces its action by sending unfolded and/or misfolded proteins to the ubiquitin–proteasome degradation pathway and antagonizing influence on epithelial-mesenchymal transition. HSP47, on the other hand, is crucial for boosting collagen synthesis, and deposition, and fostering the emergence of fibrotic disorders. The current review aims to provide light on how HSP70 and HSP47 affect hepatic fibrogenesis. Additionally, our review looks into new therapeutic approaches that target HSP70 and HSP47 and could potentially be used as drug candidates to treat liver fibrosis, especially in cases of comorbidities.
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Metadata
Title
Targeting HSP47 and HSP70: promising therapeutic approaches in liver fibrosis management
Authors
Eslam E. Abd El-Fattah
Amr Y. Zakaria
Publication date
01-12-2022
Publisher
BioMed Central
Published in
Journal of Translational Medicine / Issue 1/2022
Electronic ISSN: 1479-5876
DOI
https://doi.org/10.1186/s12967-022-03759-z

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