Dual RNase activity of IRE1 as a target for anticancer therapies

被引:11
|
作者
Bartoszewska, Sylwia [1 ]
Slawski, Jakub [2 ]
Collawn, James F. [3 ]
Bartoszewski, Rafal [2 ]
机构
[1] Med Univ Gdansk, Dept Inorgan Chem, Gdansk, Poland
[2] Univ Wroclaw, Fac Biotechnol, Dept Biophys, F Joliot Curie 14a St, PL-50383 Wroclaw, Poland
[3] Univ Alabama Birmingham, Dept Cell Dev & Integrat Biol, Birmingham, AL 35233 USA
关键词
ER-stress; RIDD; Basal RIDD; XBP1; UPR; IRE1 & alpha; UNFOLDED PROTEIN-RESPONSE; ENDOPLASMIC-RETICULUM STRESS; PANCREATIC BETA-CELLS; CANCER STEM-CELLS; ER-STRESS; TRANSCRIPTION FACTOR; MESSENGER-RNA; TRANSMEMBRANE PROTEIN; ALLOSTERIC INHIBITION; BORTEZOMIB RESISTANCE;
D O I
10.1007/s12079-023-00784-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The unfolded protein response (UPR) is a cellular mechanism that protects cells during stress conditions in which there is an accumulation of misfolded proteins in the endoplasmic reticulum (ER). UPR activates three signaling pathways that function to alleviate stress conditions and promote cellular homeostasis and cell survival. During unmitigated stress conditions, however, UPR activation signaling changes to promote cell death through apoptosis. Interestingly, cancer cells take advantage of this pathway to facilitate survival and avoid apoptosis even during prolonged cell stress conditions. Here, we discuss different signaling pathways associated with UPR and focus specifically on one of the ER signaling pathways activated during UPR, inositol-requiring enzyme 1a (IRE1). The rationale is that the IRE1 pathway is associated with cell fate decisions and recognized as a promising target for cancer therapeutics. Here we discuss IRE1 inhibitors and how they might prove to be an effective cancer therapeutic.
引用
收藏
页码:1145 / 1161
页数:17
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