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Activation of apoptosis by caspase-3-dependent specific RelB cleavage in anticancer agent-treated cancer cells: Involvement of positive feedback mechanism

机译:caspase-3依赖的特异性RelB裂解在抗癌剂治疗的癌细胞中激活细胞凋亡:积极反馈机制的参与

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摘要

DTCM-glutarimide (DTCM-G) is a newly found anti-inflammatory agent. In the course of experiments with lymphoma cells, we found that DTCM-G induced specific RelB cleavage. Anticancer agent vinblastine also induced the specific RelB cleavage in human fibrosarcoma HT1080 cells. The site-directed mutagenesis analysis revealed that the Asp205 site in RelB was specifically cleaved possibly by caspase-3 in vinblastine-treated HT1080 cells. Moreover, the cells stably overexpressing RelB Asp205Ala were resistant to vinblastine-induced apoptosis. Thus, the specific Asp205 cleavage of RelB by caspase-3 would be involved in the apoptosis induction by anticancer agents, which would provide the positive feedback mechanism. (C) 2014 Elsevier Inc. All rights reserved.
机译:DTCM-戊二酰亚胺(DTCM-G)是新发现的抗炎药。在淋巴瘤细胞的实验过程中,我们发现DTCM-G诱导特异性RelB裂解。抗癌剂长春碱还诱导人纤维肉瘤HT1080细胞中的特异性RelB裂解。定点诱变分析显示,在长春碱处理的HT1080细胞中,RelB中的Asp205位点可能被caspase-3特异性切割。此外,稳定表达RelB Asp205Ala的细胞对长春碱诱导的凋亡具有抗性。因此,caspase-3对RelB的特异性Asp205切割将参与抗癌剂的凋亡诱导,这将提供积极的反馈机制。 (C)2014 Elsevier Inc.保留所有权利。

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