中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
A novel dithiocarbamate derivative induces cell apoptosis through p53-dependent intrinsic pathway and suppresses the expression of the E6 oncogene of human papillomavirus 18 in HeLa cells

文献类型:期刊论文

作者Li, YH (Li, Yanhong); Qi, HX (Qi, Hongxue); Li, XB (Li, Xiaobo); Hou, XL (Hou, Xueling); Lu, XY (Lu, Xueying); Xiao, XW (Xiao, Xiangwen)
刊名APOPTOSIS
出版日期2015
卷号20期号:6页码:787-795
关键词Dithiocarbamate derivative Apoptosis Caspase P53-Dependent intrinsic pathway HPV18 E6
ISSN号1360-8185
通讯作者Li, XB
中文摘要Dithiocarbamates (DTCs) exhibit a broad spectrum of antitumor activities, however, their molecular mechanisms of antitumor have not yet been elucidated. Previously, we have synthesized a series of novel dithiocarbamate derivatives. These DTCs were examined for cytotoxic activities against five human cancer cell lines. In this study, one of dithiocarbamate (DTC1) with higher potential for HeLa cells was chosen to investigate molecular mechanisms for its anti-tumor activities. DTC1 could inhibit proliferation, and highly induce apoptosis in HeLa cells by activating caspase-3, -6 and -9; moreover, activities of caspase-3, -6 and -9 were inhibited by pan-caspase inhibitor, Z-VAD-FMK. Furthermore, DTC1 decreased the levels of Bcl-2 and Bcl-xL, and increased expression of cytosol cytochrome c, Bak, Bax and p53 in a time-dependent manner but had no effect on the level of Rb. It was shown that DTC1 induced HeLa cells apoptosis through a p53-dependent pathway as tested by the wild type p53 inhibitor, pifithrin-alpha. Additionally, the relative expression of E6 and E7 were evaluated in HPV18-positive (HeLa cells) by real-time PCR and western blotting. The results firstly demonstrated that DTC1 suppressed both expression of E6 mRNA and E6 oncoprotein, but had no effect on the expression of E7 mRNA and protein in HPV18. Our results suggested that DTC1 may serve as novel chemotherapeutic agents in the treatment of cervical cancer and potential anti-HPV virus candidates that merit further studies.
收录类别SCI
资助信息Natural Science Foundation of Xinjiang Uygur Autonomous Region;Western Action Project of Bureau of Resources and Environmental Science, Chinese Academy of Sciences, P. R. China
公开日期2015-07-11
源URL[http://ir.xjipc.cas.cn/handle/365002/4296]  
专题新疆理化技术研究所_省部共建新疆特有药用资源利用重点实验室
新疆理化技术研究所_资源化学研究室
作者单位Chinese Acad Sci, Xinjiang Tech Inst Phys & Chem, Key Lab Chem Plant Resources Arid Reg, Urumqi 830011, Peoples R China
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GB/T 7714
Li, YH ,Qi, HX ,Li, XB ,et al. A novel dithiocarbamate derivative induces cell apoptosis through p53-dependent intrinsic pathway and suppresses the expression of the E6 oncogene of human papillomavirus 18 in HeLa cells[J]. APOPTOSIS,2015,20(6):787-795.
APA Li, YH ,Qi, HX ,Li, XB ,Hou, XL ,Lu, XY ,&Xiao, XW .(2015).A novel dithiocarbamate derivative induces cell apoptosis through p53-dependent intrinsic pathway and suppresses the expression of the E6 oncogene of human papillomavirus 18 in HeLa cells.APOPTOSIS,20(6),787-795.
MLA Li, YH ,et al."A novel dithiocarbamate derivative induces cell apoptosis through p53-dependent intrinsic pathway and suppresses the expression of the E6 oncogene of human papillomavirus 18 in HeLa cells".APOPTOSIS 20.6(2015):787-795.

入库方式: OAI收割

来源:新疆理化技术研究所

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