Multiple pathways were involved in tubeimoside-1-induced cytotoxicity of HeLa cells

被引:28
作者
Xu, Yang [1 ,2 ]
Ching, Yick-Pang [3 ]
Zhou, Yuan [3 ]
Chiu, Jen-Fu [3 ,7 ]
Chen, Feng [1 ,4 ]
He, Qing-Yu [5 ,6 ]
机构
[1] Univ Hong Kong, Sch Biol Sci, Hong Kong, Hong Kong, Peoples R China
[2] Xiamen Univ, Sch Pharmaceut Sci, Xiamen 361005, Peoples R China
[3] Univ Hong Kong, Dept Anat, Hong Kong, Hong Kong, Peoples R China
[4] Peking Univ, Coll Engn, Inst Food & Bioresource Engn, Beijing 100871, Peoples R China
[5] Jinan Univ, Inst Life & Hlth Engn, Guangzhou 510632, Guangdong, Peoples R China
[6] Jinan Univ, Natl Engn Res Ctr Genet Med, Guangzhou 510632, Guangdong, Peoples R China
[7] Shantou Univ, Coll Med, Open Lab Tumor Mol Biol, Shantou 515041, Peoples R China
基金
中国国家自然科学基金;
关键词
Cytoskeleton; Cytotoxicity; ER; Mitochondria; Tubeimoside-1; MITOCHONDRIAL PERMEABILITY TRANSITION; ENDOPLASMIC-RETICULUM STRESS; DNA-DAMAGE CHECKPOINT; KINASE-ACTIVITY; CYCLE ARREST; TRITERPENOID SAPONINS; CARCINOMA-CELLS; BINDING-SITE; APOPTOSIS; PHOSPHORYLATION;
D O I
10.1016/j.jprot.2011.08.014
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The Bolbostemma paniculatum (Maxim.) Franquet (Cucurbitaceae) is a Chinese herb with anticancer potential. Its main active component tubeimoside-1 (TBMS1), a triterpenoid saponin, was previously proved as a potent anticancer chemotherapeutic agent; however, the molecular basis for its activities is still elusive. In the present study, subcellular proteomic study in the cytoplasm and membrane protein fractions extracted from HeLa cells revealed that proteins act as mediators of ROS generation and Ca(2+) regulation were substantially altered in expression upon TBMS1 stimuli. We also found that TBMS1 induced cell cycle arrest at G2/M phase accompanied by a decrease in GO/G1 phase in HeLa cells. Further biochemical studies showed that TBMS1 inhibited the levels of cyclinB1, Cdc2 and Cdc25C, but enhanced Chk2 phosphorylation. In addition, the cytoplasm sequestration of Cdc25C, Cip1/p21 induction and tubulin dyspolymerization also contributed to the TBMS1-mediated cell cycle arrest on the G2/M phase. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:491 / 501
页数:11
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