TPD7 inhibits the non-small cell lung cancer HCC827 cell growth by regulating EGFR signalling pathway

被引:1
|
作者
Zhang, Xiaoyan [1 ]
Zhang, Hongjun [1 ]
Qi, Gangqiang [1 ]
Gu, Xing [1 ]
Zhao, Yanjun [1 ]
Zhang, Jie [2 ]
机构
[1] Xian Chest Hosp, Dept Pulm & Crit Care Med, Xian, Shaanxi, Peoples R China
[2] Xian Int Med Ctr Hosp, Dept Oncol, Xian 710100, Shaanxi, Peoples R China
关键词
TPD7; lung cancer; HCC827; EGFR; cell growth; ET-RHIZOMA-LEONTICIS; BREAST-CANCER; IN-VITRO; TASPINE; PROLIFERATION; SUPPRESSES; EXPRESSION; RESISTANCE; INVASION;
D O I
10.1080/1120009X.2021.1945790
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Non-small cell lung cancer (NSCLC) accounts for 85% of lung cancer cases, and is characterized by more insensitivity to chemotherapy and poor prognosis. Epidermal growth factor receptor (EGFR) has been confirmed as a tumorigenic driving factor of NSCLC. Taspine has been proved effective in the inhibition of malignant tumours. Here, we found TPD7, a novel taspine derivative, exerted most inhibitory effect on EGFR-dependent HCC827 cells and investigated the underling mechanism. In addition, TPD7 could block cell cycle at G0/G1 phase of HCC827 cells by regulating the expression of cyclin D1 and cyclin E. Furthermore, TPD7 induced HCC827 cell apoptosis by regulating the expression of BCL-2 family proteins. Further study revealed that TPD7 could down-regulate the phosphorylation of EGFR and downstream members. TPD7 might present a potential EGFR inhibitor in the treatment of NSCLC.
引用
收藏
页码:110 / 116
页数:7
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