4.7 Review

The pathogenesis of organ fibrosis: Focus on necroptosis

Journal

BRITISH JOURNAL OF PHARMACOLOGY
Volume 180, Issue 22, Pages 2862-2879

Publisher

WILEY
DOI: 10.1111/bph.15952

Keywords

liver fibrosis; lung fibrosis; MLKL; necroptosis; RIPK1; 3; tissue fibrosis

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Fibrosis is a common response to chronic progressive diseases, characterized by excessive deposition of extracellular matrix. Different types of cell death are closely related to organ fibrosis, among which necroptosis is considered as a potential target to ameliorate fibrosis.
Fibrosis is a common process of tissue repair response to multiple injuries in all chronic progressive diseases, which features with excessive deposition of extracellular matrix. Fibrosis can occur in all organs and tends to be nonreversible with the progress of the disease. Different cells types in different organs are involved in the occurrence and development of fibrosis, that is, hepatic stellate cells, pancreatic stellate cells, fibroblasts and myofibroblasts. Various types of programmed cell death, including apoptosis, autophagy, ferroptosis and necroptosis, are closely related to organ fibrosis. Among these programmed cell death types, necroptosis, an emerging regulated cell death type, is regarded as a huge potential target to ameliorate organ fibrosis. In this review, we summarize the role of necroptosis signalling in organ fibrosis and collate the small molecule compounds targeting necroptosis. In addition, we discuss the potential challenges, opportunities and open questions in using necroptosis signalling as a potential target for antifibrotic therapies.

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