FPHPB inhibits gastric tumor cell proliferation by inducing G2-M cell cycle arrest

被引:10
|
作者
Xue, Lei [1 ]
Wu, Zhijun [2 ]
Liu, Jinyuan [1 ]
Luo, Jinhua [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Thorac Surg, Nanjing 210009, Jiangsu, Peoples R China
[2] Nantong Tumor Hosp, Dept Radiotherapy, Nantong 226361, Jiangsu, Peoples R China
关键词
FPHPB; Gastric tumor cells; Proliferation; Apoptosis; Cell cycle; CANCER-CELLS; PHOSPHORYLATION; ACTIVATION; CHECKPOINT; APOPTOSIS; PACLITAXEL; DOCETAXEL; PATHWAYS; MITOSIS; CDC25;
D O I
10.1016/j.biopha.2017.12.106
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Gastric cancer is a common cancer in the world with high morbidity and mortality. Here, we report that FPHPB (4-(4-(2-fluoropyridin-3-yl) phenyl)-N-(4-hydroxyphenyl)), a derivative of CMPD-1/MK2a Inhibitor, had antitumor activities by inhibiting gastric tumor SNU-16 and SGC7901 cells. FPHPB dose-dependently inhibited cell proliferation, induced cell apoptosis and arrested SNU-16 and SGC7901 cells in G2-M cell cycle checkpoint. Upon treatment with FPHPB, apoptotic proteins cleaved PARP and cleaved caspase-3 were remarkably increased, and G2-M regulatory molecules, the phosphorylation of Cdc2 and Chk2, were significantly accentuated. Collectively, FPHPB has anti-tumor activities and may be a potential candidate for treating gastric cancers.
引用
收藏
页码:694 / 700
页数:7
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