Blocking inhibition to YAP by ActinomycinD enhances anti-tumor efficacy of Corosolic acid in treating liver cancer

被引:22
|
作者
Xu, Yanfeng [1 ]
Zhao, Yinghui [2 ]
Xu, Yanli [3 ]
Guan, Yu [4 ]
Zhang, Xiao [2 ]
Chen, Yan [2 ]
Wu, Qi [2 ]
Zhu, Guoqing [2 ]
Chen, Yuxin [2 ]
Sun, Fenyong [2 ]
Wang, Jiayi [2 ,5 ]
Yu, Yongchun [6 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Shanghai Municipal Hosp Tradit Chinese Med, Dept Pharm, Shanghai 200071, Peoples R China
[2] Tongji Univ, Sch Med, Shanghai Peoples Hosp 10, Dept Clin Lab, Shanghai 200072, Peoples R China
[3] Dongjing Town Community Hlth Serv Ctr Songjiang D, Dept Pharm, Shanghai 201619, Peoples R China
[4] Shanghai Univ Tradit Chinese Med, Shanghai Municipal Hosp Tradit Chinese Med, Dept Expt Ctr, Shanghai 200071, Peoples R China
[5] Tongji Univ, Adv Inst Translat Med, Shanghai 200092, Peoples R China
[6] Shanghai Univ Tradit Chinese Med, Shanghai Municipal Hosp Tradit Chinese Med, Shanghai 200071, Peoples R China
基金
中国国家自然科学基金;
关键词
Chemotherapy; YAP; Protein stability; Transformative phenotypes; beta TrCP; HEPATOCELLULAR-CARCINOMA CELLS; TRADITIONAL CHINESE MEDICINE; UBIQUITIN E3 LIGASES; LONG NONCODING RNA; BETA-TRCP; STIMULATES TUMORIGENESIS; APOPTOSIS; DOXORUBICIN; CATENIN; SMURF1;
D O I
10.1016/j.cellsig.2016.11.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Chemotherapy is critical for the treatment of liver cancer. Despite the pro-apoptotic effects of corosolic acid (CA) have been revealed, the methods to enhance its efficacy are unclear. The aim of this study is to investigate the target that might reduce CA efficacy and figure out the way to conquer it. We found reduction of Yes-associated protein (YAP) might be a critical event that suppresses efficacy of CA. Treatment of CA accelerated degradation of YAP via enhancing its phosphorylation by LATS1. Moreover, we found CA boosts beta TrCP-dependent Ubiquitination of YAP. Interestingly, the protein stability of beta TrCP per se could be enhanced by CA. Notably, ActionomycinD (AD) strengthened CA-induced apoptosis of liver cancer cells via elevating YAP while down-regulating beta TrCP. Importantly, combined treatment of CA and AD had much more obvious influences against trans formative phenotypes of liver cancer cells than those under treatment of CA alone. Combined usage of AD successfully reduced IC50 value of CA. In summary, we have first uncovered that suppression of YAP might reduce efficacy of CA to treat liver cancer, combined treatment of AD and CA might solve this problem. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:209 / 217
页数:9
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