MicroRNA-429 Modulates Hepatocellular Carcinoma Prognosis and Tumorigenesis

被引:42
作者
Huang, Xiao-Ying [1 ]
Yao, Jin-Guang [1 ]
Huang, Hong-Dong [2 ]
Wang, Chao [3 ]
Ma, Yun [4 ]
Xia, Qiang [5 ]
Long, Xi-Dai [1 ,5 ]
机构
[1] Youjiang Med Coll Nationalities, Dept Pathol, Baise 533000, Peoples R China
[2] Capital Med Univ, Beijing Shijitan Hosp, Div Nephrol, Beijing 100038, Peoples R China
[3] Youjiang Med Coll Nationalities, Affiliated Hosp, Dept Med, Baise 533000, Peoples R China
[4] Guangxi Med Univ, Affiliated Hosp 1, Dept Pathol, Nanning 530021, Peoples R China
[5] Shanghai Jiao Tong Univ, Sch Med, Renji Hosp, Dept Liver Surg, Shanghai 200127, Peoples R China
基金
中国国家自然科学基金;
关键词
COLORECTAL-CANCER; GASTRIC-CANCER; POLYMORPHISMS; EXPRESSION; MIR-429; NETWORKS; TARGETS; BIOLOGY; GROWTH;
D O I
10.1155/2013/804128
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
MicroRNA-429 (miR-429) may modify the development and progression of cancers; however, the role of this microRNA in the hepatocellular carcinoma (HCC) has not been well elaborated. Here, we tested miR-429 expression in 138 pathology-diagnosed HCC cases and SMMC-7721 cells. We found that miR-429 was upregulated in HCC tumor tissues and that the high expression of miR-429 was significantly correlated with larger tumor size (odd ratio (OR), 2.70; 95% confidence interval (CI), 1.28-5.56) and higher aflatoxin B1-DNA adducts (OR = 3.13, 95% CI = 1.47-6.67). Furthermore, this microRNA overexpression modified the recurrence-free survival and overall survival of HCC patients. Functionally, miR-429 overexpression progressed tumor cells proliferation and inhibited cell apoptosis. These results indicate for the first time that miR-429 may modify HCC prognosis and tumorigenesis and may be a potential tumor therapeutic target.
引用
收藏
页数:10
相关论文
共 45 条
[1]   Modeling microRNA-Transcription Factor Networks in Cancer [J].
Aguda, Baltazar D. .
MICRORNA CANCER REGULATION: ADVANCED CONCEPTS, BIOINFORMATICS AND SYSTEMS BIOLOGY TOOLS, 2013, 774 :149-167
[2]  
[Anonymous], CHINESE CLIN ONCOLOG
[3]   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
[4]   Role of MicroRNAs in Lung Cancer MicroRNA Signatures in Cancer Prognosis [J].
Boeri, Mattia ;
Pastorino, Ugo ;
Sozzi, Gabriella .
CANCER JOURNAL, 2012, 18 (03) :268-274
[5]   A double-negative feedback loop between ZEB1-SIP1 and the microRNA-200 family regulates epithelial-mesenchymal transition [J].
Bracken, Cameron P. ;
Gregory, Philip A. ;
Kolesnikoff, Natasha ;
Bert, Andrew G. ;
Wang, Jun ;
Shannon, M. Frances ;
Goodall, Gregory J. .
CANCER RESEARCH, 2008, 68 (19) :7846-7854
[6]   Overexpression of miR-429 induces mesenchymal-to-epithelial transition (MET) in metastatic ovarian cancer cells [J].
Chen, Jing ;
Wang, Lijuan ;
Matyunina, Lilya V. ;
Hill, Christopher G. ;
McDonald, John F. .
GYNECOLOGIC ONCOLOGY, 2011, 121 (01) :200-205
[7]   Non-coding RNAs in human disease [J].
Esteller, Manel .
NATURE REVIEWS GENETICS, 2011, 12 (12) :861-874
[8]   Hallmarks of Cancer: The Next Generation [J].
Hanahan, Douglas ;
Weinberg, Robert A. .
CELL, 2011, 144 (05) :646-674
[9]   Multiple-to-Multiple Relationships between MicroRNAs and Target Genes in Gastric Cancer [J].
Hashimoto, Yutaka ;
Akiyama, Yoshimitsu ;
Yuasa, Yasuhito .
PLOS ONE, 2013, 8 (05)
[10]   MiR-200b and miR-429 Function in Mouse Ovulation and Are Essential for Female Fertility [J].
Hasuwa, Hidetoshi ;
Ueda, Jun ;
Ikawa, Masahito ;
Okabe, Masaru .
SCIENCE, 2013, 341 (6141) :71-73