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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.
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页码:110 / 116
页数:7
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