Corelating the molecular structure of BAG3 to its oncogenic role

被引:0
|
作者
Pattoo, Tabinda Showkat [1 ]
Khanday, Firdous A. [1 ]
机构
[1] Univ Kashmir, Dept Biotechnol, Srinagar, Jammu & Kashmir, India
关键词
apoptosis; cancer; chaperone; oxidative stress; protein structure/assembly; CANCER-CELLS; INDUCED APOPTOSIS; DOWN-MODULATION; PROTEIN BAG3; MESENCHYMAL TRANSITION; SELECTIVE AUTOPHAGY; THERAPEUTIC TARGET; PANCREATIC-CANCER; QUALITY-CONTROL; MESSENGER-RNA;
D O I
10.1002/cbin.12199
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
BAG3 is a multifaceted protein characterised by having WW domain, PXXP motif and BAG domain. This protein gets upregulated during malignant transformation of cells and has been associated with poorer survival of patients. Procancerous activity of BAG domain of BAG3 is well documented. BAG domain interacts with ATPase domain of Hsp-70 preventing protein delivery to proteasome. This impediment results in enhanced cell survival, proliferation, resistance to apoptosis and chemoresistance. Besides BAG domain other two domains/motifs of BAG3 are under research vigilance to explore its further oncogenic role. This review summarises the role of different structural determinants of BAG3 in elevating oncogenesis. Based on the already existing findings, more interacting partners of BAG3 are anticipated. The anticipated partners of BAG3 can shed a wealth of information into the mechanistic insights of its proproliferative role. Proper insights into the mechanistic details adopted by BAG3 to curtail/elaborate activity of anticipated interacting partners can serve as a potent target for development of therapeutic interventions.
引用
收藏
页码:1080 / 1096
页数:17
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