Targeting necroptosis in fibrosis

被引:5
作者
Hassanein, Emad H. M. [1 ]
Ibrahim, Islam M. [2 ]
El-Maksoud, Mostafa S. Abd [2 ]
El-Aziz, Mostafa K. Abd [2 ]
Abd-alhameed, Esraa K. [3 ]
Althagafy, Hanan S. [4 ]
机构
[1] Al Azhar Univ, Fac Pharm, Dept Pharmacol & Toxicol, Assiut, Egypt
[2] Al Azhar Univ, Fac Pharm, Assiut Branch, Assiut 71524, Egypt
[3] Beni Suef Univ, Dept Pharmacol & Toxicol, Fac Pharm, Bani Suwayf, Egypt
[4] Univ Jeddah, Fac Sci, Dept Biochem, Jeddah, Saudi Arabia
关键词
Necroptosis; Fibrosis; RIPK1; RIPK3; MLKL; FIBRILLARY ACIDIC PROTEIN; HEPATIC STELLATE CELLS; MIXED LINEAGE KINASE; EXTRACELLULAR-MATRIX; OXIDATIVE STRESS; NECROSTATIN-1; PROTECTS; INTERSTITIAL FIBROSIS; MOLECULAR-MECHANISMS; PROGRAMMED NECROSIS; LIVER FIBROSIS;
D O I
10.1007/s11033-023-08857-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Necroptosis, a type of programmed cell death that resembles necrosis, is now known to depend on a different molecular mechanism from apoptosis, according to several recent studies. Many efforts have reported the possible influence of necroptosis in human disorders and concluded the crucial role in the pathophysiology of various diseases, including liver diseases, renal injuries, cancers, and others. Fibrosis is the most common end-stage pathological cascade of several chronic inflammatory disorders. In this review, we explain the impact of necroptosis and fibrosis, for which necroptosis has been demonstrated to be a contributing factor. We also go over the inhibitors of necroptosis and how they have been applied to fibrosis models. This review helps to clarify the role of necroptosis in fibrosis and will encourage clinical efforts to target this pathway of programmed cell death.
引用
收藏
页码:10471 / 10484
页数:14
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