Association of microRNA-3144 variant with the susceptibility to hepatocellular carcinoma

被引:0
|
作者
Jun Zhang
Rui Wang
Min Cai
Shunji Yu
Yanyun Ma
Weihong Xu
Chunfang Gao
Jiucun Wang
Lifang Hou
Yi Liu
Jie Liu
机构
[1] Fudan University,Department of Digestive Diseases, Huashan Hospital
[2] Fudan University,Department of Immunology of Shanghai Medical School and Institutes of Biomedical Sciences
[3] Fudan University,Ministry of Education Key Laboratory of Contemporary Anthropology and State Key Laboratory of Genetic Engineering, School of Life Sciences
[4] Tongji University School of Medicine,Department of Digestive Diseases, Yangpu Hospital
[5] Shanghai Tongren Hospital,Department of Clinical Laboratory
[6] Second Military Medical University,Eastern Hepatobiliary Surgery Hospital
[7] Northwestern University,Department of Preventive Medicine, Feinberg School of Medicine
[8] Northwestern University,Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine
来源
Genes & Genomics | 2014年 / 36卷
关键词
Hepatocellular carcinoma; MicroRNA-3144; Single nucleotide polymorphism; Alpha fetoprotein;
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中图分类号
学科分类号
摘要
Increasing studies suggest that microRNAs, a new group of small non-coding molecules, regulate the expression of their target genes and play some roles in cancers. Thus, it is hypothesized that the genetic variants of microRNAs could contribute to the susceptibility to cancers. In this study, the association between rs67106263 in microRNA-3144 and the risk of hepatocellular carcinoma (HCC) was explored in a large-scaled case–control population based on MassARRAY technology. It was discovered that compared with the carriers of wide-type GG genotype and heterozygote GA genotype of microRNA-3144, the significantly increased risk of HCC was observed in the subjects with the homozygote variant AA (adjusted odds ratio = 1.285, 95 % confidence interval = 1.004–1.643, P = 0.046). Additionally, the variant was also associated with the expression of alpha fetoprotein (AFP), which is the diagnostic marker for HCC. Our findings suggest for the first time that rs67106263 may play some roles in the risk of HCC, expecting future molecular researches to elucidate the possible mechanisms behind these results.
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页码:771 / 776
页数:5
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