自噬
三氧化二砷
胰腺癌
细胞凋亡
生物
癌症研究
溴尿嘧啶
程序性细胞死亡
恶性肿瘤
癌症
基因敲除
癌细胞
表观遗传学
生物化学
遗传学
基因
作者
Congling Xu,Xinrui Wang,Yu Zhou,Fei Chen,Haiwei Wang,Kening Li,Huiyong Fan,Xiaomei Tang,Guojuan Jiang,Ji Zhang
出处
期刊:Oncogene
[Springer Nature]
日期:2019-08-16
卷期号:38 (47): 7249-7265
被引量:27
标识
DOI:10.1038/s41388-019-0930-3
摘要
Pancreatic cancer is a deadliest type of malignancy and lacks effective intervention. We here report a potential strategy for treatment of this malignancy by the combination of arsenic trioxide (ATO) and BET bromodomain inhibitor JQ1. These two agents synergistically modulate multistages of autophagy and thus induce apoptosis effectively in pancreatic cancer cells. Our genomic and biochemical data have demonstrated that crosstalks between ER stress and autophagy play crucial roles during ATO-induced apoptosis, in which NRF2 may stand at the crossroad between cell death and survival. This has been further strengthened by our finding that NRF2 depletion renders insensitive cells into sensitive ones in regard to ATO treatment-caused cell death. The knockdown of NRF2 and the addition of JQ1 result in similar molecular/cellular effects in promoting effective ATO-induced apoptosis in cells that are insensitive to ATO treatment alone. Thus, the combination of ATO and JQ1 may represent a new treatment strategy for pancreatic cancer.
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