Mir-1287 suppresses the proliferation, invasion, and migration in hepatocellular carcinoma by targeting PIK3R3

被引:28
作者
Lu, Junhao [1 ]
Tang, Licheng [1 ]
Xu, Yuqiang [2 ]
Ge, Kuikui [1 ]
Huang, Jinjiang [2 ]
Gu, Meigang [3 ]
Zhong, Jiang [1 ]
Huang, Qingshan [1 ,2 ]
机构
[1] Fudan Univ, Sch Life Sci, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
[2] Shanghai High Tech United Biotechnol R&D Co Ltd, Shanghai, Peoples R China
[3] Rockefeller Univ, Lab Virol & Infect Dis, Ctr Study Hepatitis C, 1230 York Ave, New York, NY 10021 USA
关键词
cell proliferation; hepatocellular carcinoma; mir-1287; PIK3R3; tumor metastasis; REGULATORY SUBUNIT; MESENCHYMAL TRANSITION; CELL-PROLIFERATION; CANCER STATISTICS; MICRORNAS; IDENTIFICATION; INHIBITOR; PATHOGENESIS; P55-GAMMA; GROWTH;
D O I
10.1002/jcb.27190
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mature microRNAs (miRNAs) are a class of small noncoding RNA molecules involved in regulation of post-translational gene expression. Although aberrant levels of miRNAs have been found in various tumor tissues, their importance in tumor development and the molecular basis of their regulatory role remain unclear. Our bioinformatic analysis on The Cancer Genome Atlas database and microarray-based comparison of miRNA in different cell lines revealed that the level of mir-1287 is suppressed in hepatocellular carcinoma (HCC) cells. When upregulated, mir-1287 can reduce the tumorigenesis phenotypes of HCC cells in several in vitro models. We further found that mir-1287 directly targets messenger RNA encoding PIK3R3, which is a tumor-promoting factor acting in several pathways linked to tumorigenesis. Our study suggests that aberrant suppression of mir-1287 is potentially responsible for the development of HCC, and miRNA-based strategies may be developed for efficient detection and treatment of HCC.
引用
收藏
页码:9229 / 9238
页数:10
相关论文
共 32 条
[1]  
[Anonymous], COLD SPRING HARB PER
[2]   MicroRNAs in liver cancer: a model for investigating pathogenesis and novel therapeutic approaches [J].
Callegari, E. ;
Gramantieri, L. ;
Domenicali, M. ;
D'Abundo, L. ;
Sabbioni, S. ;
Negrini, M. .
CELL DEATH AND DIFFERENTIATION, 2015, 22 (01) :46-57
[3]   MiR-511 inhibits growth and metastasis of human hepatocellular carcinoma cells by targeting PIK3R3 [J].
Cao, Gang ;
Dong, Weihua ;
Meng, Xiaoxi ;
Liu, Hongchao ;
Liao, Huaqiang ;
Liu, Shiyuan .
TUMOR BIOLOGY, 2015, 36 (06) :4453-4459
[4]   Cancer Statistics in China, 2015 [J].
Chen, Wanqing ;
Zheng, Rongshou ;
Baade, Peter D. ;
Zhang, Siwei ;
Zeng, Hongmei ;
Bray, Freddie ;
Jemal, Ahmedin ;
Yu, Xue Qin ;
He, Jie .
CA-A CANCER JOURNAL FOR CLINICIANS, 2016, 66 (02) :115-132
[5]   Task Allocation and Path Planning for Collaborative Autonomous Underwater Vehicles Operating through an Underwater Acoustic Network [J].
Deng, Yueyue ;
Beaujean, Pierre-Philippe J. ;
An, Edgar ;
Carlson, Edward .
JOURNAL OF ROBOTICS, 2013, 2013
[6]   Serine protease inhibitor kazal-type 6 inhibits tumorigenesis of human hepatocellular carcinoma cells via its extracellular action [J].
Ge, Kuikui ;
Huang, Jinjiang ;
Wang, Wei ;
Gu, Meigang ;
Dai, Xinchuan ;
Xu, Yuqiang ;
Wu, Hongyu ;
Li, Guodong ;
Lu, Hairong ;
Zhong, Jiang ;
Huang, Qingshan .
ONCOTARGET, 2017, 8 (04) :5965-5975
[7]   A peptide inhibitor derived from p55PIK phosphatidylinositol 3-kinase regulatory subunit: a novel cancer therapy [J].
Hu, Junbo ;
Xia, Xianmin ;
Cheng, Aiwu ;
Wang, Guihua ;
Luo, Xuelai ;
Reed, Michael F. ;
Fojo, Tito ;
Oetting, Alexis ;
Gong, Jianping ;
Yen, Paul M. .
MOLECULAR CANCER THERAPEUTICS, 2008, 7 (12) :3719-3728
[8]   Cancer statistics, 2007 [J].
Jemal, Ahmedin ;
Siegel, Rebecca ;
Ward, Elizabeth ;
Murray, Taylor ;
Xu, Jiaquan ;
Thun, Michael J. .
CA-A CANCER JOURNAL FOR CLINICIANS, 2007, 57 (01) :43-66
[9]   MicroRNA-190 regulates FOXP2 genes in human gastric cancer [J].
Jia, Wen-Zhuo ;
Yu, Tao ;
An, Qi ;
Yang, Hua ;
Zhang, Zhu ;
Liu, Xiao ;
Xiao, Gang .
ONCOTARGETS AND THERAPY, 2016, 9 :3643-3651
[10]   Transcriptional regulation of the cyclin D1 gene at a glance [J].
Klein, Eric A. ;
Assoian, Richard K. .
JOURNAL OF CELL SCIENCE, 2008, 121 (23) :3853-3857