Role of inhibitor of yes-associated protein 1 in triple-negative breast cancer with taxol-based chemoresistance

被引:33
|
作者
Li, Ying [1 ]
Wang, Shunan [2 ]
Wei, Xi [3 ]
Zhang, Sheng [1 ]
Song, Zian [1 ]
Chen, Xiao [1 ]
Zhang, Jin [1 ]
机构
[1] Tianjin Med Univ, Key Lab Breast Canc Prevent & Therapy,Key Lab Can, Natl Clin Res Ctr Canc,Tianjins Clin Res Ctr Canc, Surg Dept Breast Canc 3,Canc Inst & Hosp,Minist E, Tianjin, Peoples R China
[2] Army Med Univ, Daping Hosp, Dept Radiol, Chongqing, Peoples R China
[3] Tianjin Med Univ, Canc Inst & Hosp, Key Lab Canc Prevent & Therapy,Dept Diagnost & Th, Tianjins Clin Res Ctr Canc,Natl Clin Res Ctr Canc, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
chemoresistance; inhibitor; taxol; triple-negative breast cancer; YAP1; YAP; PATHWAY; APOPTOSIS; ONCOGENE; YORKIE;
D O I
10.1111/cas.13888
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Triple-negative breast cancer (TNBC) is highly clinically aggressive and taxol-based chemoresistance remains a big TNBC therapeutic problem to be solved. Verteporfin, a small molecular yes-associated protein 1 (YAP1) inhibitor, is little known as an antitumor drug for TNBC. Our data showed that YAP1 expression was associated with early relapse in tissue samples of patients with TNBC taxol chemoresistance (P < .001). Verteporfin reduced migration and enhanced apoptosis or autophagy of a taxol-resistant MDA-MB-231 cell line in vitro. Knockdown of YAP1 increased epithelial-mesenchymal transition response in a taxol-resistant TNBC cell line. In an in vivo experiment, we found that verteporfin was able to shrink tumor weight and volume and decreased Ki67 expression in a taxol-resistant mouse model. Our results provide evidence that verteporfin could be a chemosensitizer for TNBC patients with taxol-based treatment.
引用
收藏
页码:561 / 567
页数:7
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