Hypoxia induces autophagy in PA-1 ovarian teratoma cells and resistance to growth inhibition and apoptosis by chemotherapeutic agent cis-diamminedichloroplatinum

被引:8
|
作者
Chen, C. D. [1 ,2 ,3 ]
Dai, L. N. [2 ,3 ]
Wang, M. [2 ,3 ]
Lai, X. H. [4 ]
Wang, J. [1 ]
机构
[1] Soochow Univ, Childrens Hosp, Dept Pediat Surg, 92 Zhongnan St, Suzhou 215003, Jiangsu, Peoples R China
[2] Wenzhou Med Univ, Dept Pediat Surg, Affiliated Hosp 2, Wenzhou, Peoples R China
[3] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou, Peoples R China
[4] Wenzhou Med Univ, Affiliated Hosp 1, Inst Inflammat & Dis, Wenzhou, Peoples R China
关键词
Malignant teratoma; Hypoxia; Autophagy; Chemotherapy; INDUCIBLE FACTORS; CANCER;
D O I
10.12892/ejgo3582.2017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pathological hypoxia exists in solid tumors and it creates a microenvironment for tumor cells which has a critical and complicated implication for cancer. Hypoxia can also activate autophagy which plays a dual role in cancer. In this study the authors analyzed the effect of hypoxia, the autophagy inhibitor 3-methyladenine (3-MA), cis-diamminedichloroplatinum (CDDP, cisplatin), and any combination of them on PA-1 cells (a human ovarian cancer cell line) with a series of assays, focusing on autophagy induction, cell growth inhibition, and cell death by CDDP. CDDP caused apoptosis in nonnoxic PA-1 cells and autophagy upon hypoxia treatment decreased apoptosis induction in hypoxic cells by CDDP, which has implications in cancer chemotherapy resistance.
引用
收藏
页码:277 / 281
页数:5
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