Unfolded protein response (UPR) integrated signaling networks determine cell fate during hypoxia

被引:94
作者
Bartoszewska, Sylwia [1 ]
Collawn, James F. [2 ]
机构
[1] Med Univ Gdansk, Dept Inorgan Chem, Gdansk, Poland
[2] Univ Alabama Birmingham, Dept Cell Dev & Integrat Biol, Birmingham, AL 35294 USA
关键词
ER-stress; Angiogenesis; Hypoxia-reoxygenation injury; Ischemia; Cell fate determination; UPRmt; ENDOPLASMIC-RETICULUM STRESS; ENDOTHELIAL-GROWTH-FACTOR; INDUCIBLE FACTOR-I; ISCHEMIA-REPERFUSION INJURY; MESSENGER-RNA TRANSLATION; DISULFIDE BOND FORMATION; FACTOR-A EXPRESSION; ER-STRESS; TRANSCRIPTION FACTOR; INTERMITTENT HYPOXIA;
D O I
10.1186/s11658-020-00212-1
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
During hypoxic conditions, cells undergo critical adaptive responses that include the up-regulation of hypoxia-inducible proteins (HIFs) and the induction of the unfolded protein response (UPR). While their induced signaling pathways have many distinct targets, there are some important connections as well. Despite the extensive studies on both of these signaling pathways, the exact mechanisms involved that determine survival versus apoptosis remain largely unexplained and therefore beyond therapeutic control. Here we discuss the complex relationship between the HIF and UPR signaling pathways and the importance of understanding how these pathways differ between normal and cancer cell models.
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页数:20
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