Tian Xiaobing, Zhang Shengliang, Zhou Lanlan, Seyhan Attila A, Hernandez Borrero Liz, Zhang Yiqun, El-Deiry Wafik S
Laboratory of Translational Oncology and Experimental Cancer Therapeutics, Warren Alpert Medical School, Brown University, Providence, RI, United States.
Department of Pathology and Laboratory Medicine, Warren Alpert Medical School, Brown University, Providence, RI, United States.
Front Pharmacol. 2021 Sep 24;12:747837. doi: 10.3389/fphar.2021.747837. eCollection 2021.
The integrated stress response (ISR) is an evolutionarily conserved intra-cellular signaling network which is activated in response to intrinsic and extrinsic stresses. Various stresses are sensed by four specialized kinases, PKR-like ER kinase (PERK), general control non-derepressible 2 (GCN2), double-stranded RNA-dependent protein kinase (PKR) and heme-regulated eIF2α kinase (HRI) that converge on phosphorylation of serine 51 of eIF2α. eIF2α phosphorylation causes a global reduction of protein synthesis and triggers the translation of specific mRNAs, including activating transcription factor 4 (ATF4). Although the ISR promotes cell survival and homeostasis, when stress is severe or prolonged the ISR signaling will shift to regulate cellular apoptosis. We review the ISR signaling pathway, regulation and importance in cancer therapy.
整合应激反应(ISR)是一种进化上保守的细胞内信号网络,可响应内在和外在应激而被激活。四种特殊的激酶,即蛋白激酶R样内质网激酶(PERK)、一般控制非抑制性2(GCN2)、双链RNA依赖性蛋白激酶(PKR)和血红素调节的真核起始因子2α激酶(HRI)可感知各种应激,这些激酶最终导致真核起始因子2α的丝氨酸51位点磷酸化。真核起始因子2α磷酸化会导致蛋白质合成整体减少,并触发特定mRNA的翻译,包括激活转录因子4(ATF4)。尽管ISR促进细胞存活和体内平衡,但当应激严重或持续时,ISR信号将转向调节细胞凋亡。我们综述了ISR信号通路、调控及其在癌症治疗中的重要性。