Has-miR-30a regulates autophagic activity in cervical cancer upon hydroxycamptothecin exposure

被引:21
作者
Cheng, Yanxiang [1 ]
Chen, Gantao [1 ,2 ]
Hu, Min [1 ]
Huang, Jinling [1 ]
Li, Binshu [1 ]
Zhou, Limei [1 ]
Hong, Li [1 ]
机构
[1] Wuhan Univ, Renmin Hosp, Dept Gynecol & Obstet, Wuhan 430062, Hubei, Peoples R China
[2] Third Renmin Hosp Xiantao City, Xiaotao 433000, Hubei, Peoples R China
关键词
Hydroxycamptothecin; miR-30a; Autophagy; RAPAMYCIN-INDUCED AUTOPHAGY; DOWN-REGULATION; APOPTOSIS; MICRORNA; CELLS; 10-HYDROXYCAMPTOTHECIN; STARVATION; RESISTANCE; INHIBITOR; MIR-30A;
D O I
10.1016/j.biopha.2015.08.034
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
Cervical cancer is a leading cause of morbidity and mortality in women worldwide. Hydroxycamptothecin (HCPT) represents a new generation of antitumor agents targeting DNA topoisomerase I, which has been applied to treat various cancers with fewer side effects. Autophagy is emerging as an important biological mechanism in targeting human cancers, including cervical cancer. In this study, We have reported that HCPT could induce autophagy in Hela cells. Our investigation of the underlying mechanisms revealed that the decreased expression of miR-30a is involved in HCPT-induced autophagy. Futhermore, we showed that miR-30a could directly target a specific fragment in the 30 untranslated region of Beclin-1 as demonstrated by luciferase assay and overexpression of hsa-miR-30a by transfecting with miR-30a mimic could block HCPT-induced autophagic activity. It is the first time provide a deeper understanding of the mechanisms underlying cellular and molecular mechanisms by which HCPT affect cervical cancer. (C) 2015 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:67 / 74
页数:8
相关论文
共 38 条
[1]   Principles and Current Strategies for Targeting Autophagy for Cancer Treatment [J].
Amaravadi, Ravi K. ;
Lippincott-Schwartz, Jennifer ;
Yin, Xiao-Ming ;
Weiss, William A. ;
Takebe, Naoko ;
Timmer, William ;
DiPaola, Robert S. ;
Lotze, Michael T. ;
White, Eileen .
CLINICAL CANCER RESEARCH, 2011, 17 (04) :654-666
[2]   Autophagy: Dual roles in life and death? [J].
Baehrecke, EH .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (06) :505-510
[3]   Homocamptothecins: potent topoisomerase I inhibitors and promising anticancer drugs [J].
Bailly, C .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2003, 45 (01) :91-108
[4]   RPL13A as a reference gene for normalizing mRNA transcription of ovarian cancer cells with paclitaxel and 10-hydroxycamptothecin treatments [J].
Bian, Zehua ;
Yu, Yang ;
Quan, Chao ;
Guan, Rongwei ;
Jin, Yan ;
Wu, Jie ;
Xu, Lidan ;
Chen, Feng ;
Bai, Jing ;
Sun, Wenjing ;
Fu, Songbin .
MOLECULAR MEDICINE REPORTS, 2015, 11 (04) :3188-3194
[5]  
Boone J.D., 2015, GYNECOL ONCOL, P138
[6]   MiR-144 Inhibits Proliferation and Induces Apoptosis and Autophagy in Lung Cancer Cells by Targeting TIGAR [J].
Chen, Shanshan ;
Li, Ping ;
Li, Juan ;
Wang, Yuanyuan ;
Du, Yuwen ;
Chen, Xiaonan ;
Zang, Wenqiao ;
Wang, Huaqi ;
Chu, Heying ;
Zhao, Guoqiang ;
Zhang, Guojun .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2015, 35 (03) :997-1007
[7]   Autophagy preceded apoptosis in oridonin-treated human breast cancer MCF-7 cells [J].
Cui, Qiao ;
Tashiro, Shin-ichi ;
Onodera, Satoshi ;
Minami, Mutsuhiko ;
Ikejima, Takashi .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2007, 30 (05) :859-864
[8]   Cross talk between apoptosis and autophagy by caspase-mediated cleavage of Beclin 1 [J].
Djavaheri-Mergny, M. ;
Maiuri, M. C. ;
Kroemer, G. .
ONCOGENE, 2010, 29 (12) :1717-1719
[9]   How microRNAs choose their targets [J].
Hofacker, Ivo L. .
NATURE GENETICS, 2007, 39 (10) :1191-1192
[10]   MiR-15a and miR-16 induce autophagy and enhance chemosensitivity of Camptothecin [J].
Huang, Nunu ;
Wu, Jiangbin ;
Qiu, Wei ;
Lyu, Qing ;
He, Jie ;
Xie, Weidong ;
Xu, Naihan ;
Zhang, Yaou .
CANCER BIOLOGY & THERAPY, 2015, 16 (06) :941-948