MiR-215 modulates gastric cancer cell proliferation by targeting RB1

被引:90
作者
Deng, Yujie [1 ,2 ]
Huang, Zhenxia [3 ,4 ]
Xu, Yanjun [1 ,2 ]
Jin, Juan [1 ,2 ]
Zhuo, Wei [1 ,2 ,4 ]
Zhang, Cheng [1 ,2 ]
Zhang, Xuting [1 ,2 ]
Shen, Minhong [1 ,2 ]
Yan, Xiaoyi [1 ,2 ]
Wang, Liangjing [3 ]
Wang, Xiaojia [5 ]
Kang, Yibin [6 ]
Si, Jianmin [3 ,4 ]
Zhou, Tianhua [1 ,2 ,4 ]
机构
[1] Zhejiang Univ, Sch Med, Ctr Dis Modeling, Hangzhou 310058, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Med, Program Mol Cell Biol, Hangzhou 310058, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Sir Run Run Shaw Hosp, Clin Res Inst,Gastroenterol Lab, Hangzhou 310016, Zhejiang, Peoples R China
[4] Zhejiang Univ, Inst Gastroenterol, Hangzhou 310016, Zhejiang, Peoples R China
[5] Zhejiang Canc Hosp, Hangzhou 310022, Zhejiang, Peoples R China
[6] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
关键词
Gastric cancer; MiR-215; Retinoblastoma; Proliferation; DOWN-REGULATION; P53-INDUCIBLE MICRORNAS; MOLECULAR-BIOLOGY; CYCLE ARREST; PROTEIN; RETINOBLASTOMA; EXPRESSION; GENE; CARCINOMA; DIFFERENTIATION;
D O I
10.1016/j.canlet.2013.08.033
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Growing evidence indicates that miRNAs play critical roles in tumorigenesis and cancer progression. Here, we report that miR-215 is significantly up-regulated in gastric cancer tissues from either gastrectomy or gastroscopy. Receiver Operator Characteristic (ROC) curve analysis indicated that miR-215 may be a candidate biomarker for gastric cancer diagnosis. Inhibition of miR-215 significantly suppressed gastric cancer cell proliferation possibly via G1 arrest. Further analyses indicated that miR-215 was able to target retinoblastoma tumor-suppressor gene 1 (RB1) through its 3'-UTR in gastric cancer cells. These data suggest that frequently up-regulated miR-215 in gastric cancer may influence cell proliferation by targeting RB1. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:27 / 35
页数:9
相关论文
共 58 条
[1]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[2]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[3]   The microRNA.org resource: targets and expression [J].
Betel, Doron ;
Wilson, Manda ;
Gabow, Aaron ;
Marks, Debora S. ;
Sander, Chris .
NUCLEIC ACIDS RESEARCH, 2008, 36 :D149-D153
[4]   p53 activates the PANK1/miRNA-107 gene leading to downregulation of CDK6 and p130 cell cycle proteins [J].
Boehlig, Levin ;
Friedrich, Maik ;
Engeland, Kurt .
NUCLEIC ACIDS RESEARCH, 2011, 39 (02) :440-453
[5]   miR-192/miR-215 Influence 5-Fluorouracil Resistance through Cell Cycle-Mediated Mechanisms Complementary to Its Post-transcriptional Thymidilate Synthase Regulation [J].
Boni, Valentina ;
Bitarte, Nerea ;
Cristobal, Ion ;
Zarate, Ruth ;
Rodriguez, Javier ;
Maiello, Evaristo ;
Garcia-Foncillas, Jesus ;
Bandres, Eva .
MOLECULAR CANCER THERAPEUTICS, 2010, 9 (08) :2265-2275
[6]   p53-Responsive MicroRNAs 192 and 215 Are Capable of Inducing Cell Cycle Arrest [J].
Braun, Christian J. ;
Zhang, Xin ;
Savelyeva, Irina ;
Wolff, Sonja ;
Moll, Ute M. ;
Schepeler, Troels ;
Orntoft, Torben F. ;
Andersen, Claus L. ;
Dobbelstein, Matthias .
CANCER RESEARCH, 2008, 68 (24) :10094-10104
[7]   Emerging roles of E2Fs in cancer: an exit from cell cycle control [J].
Chen, Hui-Zi ;
Tsai, Shih-Yin ;
Leone, Gustavo .
NATURE REVIEWS CANCER, 2009, 9 (11) :785-797
[8]   Expression Levels of MicroRNA-192 and -215 in Gastric Carcinoma [J].
Chiang, Yeunpo ;
Zhou, Xin ;
Wang, Zhenning ;
Song, Yongxi ;
Liu, Zhuangkai ;
Zhao, Fang ;
Zhu, Jinliang ;
Xu, Huimian .
PATHOLOGY & ONCOLOGY RESEARCH, 2012, 18 (03) :585-591
[9]   E2f3a and E2f3b Contribute to the Control of Cell Proliferation and Mouse Development [J].
Chong, Jean-Leon ;
Tsai, Shih-Yin ;
Sharma, Nidhi ;
Opavsky, Rene ;
Price, Richard ;
Wu, Lizhao ;
Fernandez, Soledad A. ;
Leone, Gustavo .
MOLECULAR AND CELLULAR BIOLOGY, 2009, 29 (02) :414-424
[10]   Rb family proteins in gastric cancer (Review) [J].
Cito, Letizia ;
Pentimalli, Francesca ;
Forte, Iris ;
Mattioli, Eliseo ;
Giordano, Antonio .
ONCOLOGY REPORTS, 2010, 24 (06) :1411-1418