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Association of microRNA-3144 variant with the susceptibility to hepatocellular carcinoma
被引:0
|作者:
Zhang, Jun
[1
]
Wang, Rui
[1
,2
,3
]
Cai, Min
[4
]
Yu, Shunji
[1
,2
,3
]
Ma, Yanyun
[5
,6
]
Xu, Weihong
[7
]
Gao, Chunfang
[8
]
Wang, Jiucun
[5
,6
]
Hou, Lifang
[9
,10
]
Liu, Yi
[1
]
Liu, Jie
[1
,2
,3
]
机构:
[1] Fudan Univ, Huashan Hosp, Dept Digest Dis, Shanghai 200040, Peoples R China
[2] Fudan Univ, Shanghai Med Sch, Dept Immunol, Shanghai 200032, Peoples R China
[3] Fudan Univ, Inst Biomed Sci, Shanghai 200032, Peoples R China
[4] Tongji Univ, Sch Med, Yangpu Hosp, Dept Digest Dis, Shanghai 200090, Peoples R China
[5] Fudan Univ, Minist Educ, Key Lab Contemporary Anthropol, Shanghai 200433, Peoples R China
[6] Fudan Univ, Sch Life Sci, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
[7] Shanghai Tongren Hosp, Dept Clin Lab, Shanghai 200050, Peoples R China
[8] Second Mil Med Univ, Eastern Hepatobiliary Surg Hosp, Shanghai 200438, Peoples R China
[9] Northwestern Univ, Feinberg Sch Med, Dept Prevent Med, Chicago, IL 60611 USA
[10] Northwestern Univ, Feinberg Sch Med, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
关键词:
Hepatocellular carcinoma;
MicroRNA-3144;
Single nucleotide polymorphism;
Alpha fetoprotein;
CANCER;
POLYMORPHISMS;
EPIDEMIOLOGY;
D O I:
10.1007/s13258-014-0211-z
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:
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:6
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