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A genetic variant in the promoter region of miR-34b/c is associated with a reduced risk of colorectal cancer.

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机构: [1]Key Laboratory of Obstetric and Gynecologic and Pediatric Diseases and Birth Defects of Ministry of Education , Chengdu, Sichuan 610041 , P.R. China [2]Laboratory of Molecular and Translational Medicine, West China Institute of Women and Children ’ s Health, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610041 , P.R. China [3]Department of Forensic Biology , West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu, Sichuan 610041 , P.R. China [4]Department of Forensic Pathology , Henan University of Science and Technology, Luoyang, Henan 471003 , P.R. China [5]Secondary Department of General Surgery , Luo Yang Central Hospital, Luoyang, Henan 471003 , P.R. China [6]PLA Institute of Physical Education, Guangzhou, Guangdong 510502 , P.R. China
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关键词: colorectal cancer miR-34b/c polymorphism TP53

摘要:
The miR-34 family members, described as potential tumor suppressors, were downregulated in colorectal cancer (CRC). Loss of miR-34 impairs TP53-mediated cell death, while overexpression of miR-34 induces apoptosis. A potentially functional polymorphism (i.e., rs4938723T/C) in the promoter region of pri-miR-34b/c was predicted to influence the GATA-X binding sites. We aimed to investigate the association between miR-34b/c rs4938723 and TP53 Arg72Pro polymorphisms and the risk of CRC. We genotyped the two polymorphisms in 347 CRC patients and 488 healthy controls using polymerase chain reaction-restriction fragment length polymorphism and DNA sequencing assay. We found that the CC genotype and C allele of the miR-34b/c rs4938723 were associated with a significantly decreased risk of CRC compared with the TT genotype and T allele (CC vs. TT: adjusted OR=0.56; 95% CI, 0.34-0.91; C vs. T: adjusted OR=0.78; 95% CI, 0.64-0.97). In combined analysis, a borderline significance was also observed in subjects carrying the rs4938723 CT/CC and TP53 GG genotypes (adjusted OR=0.66; 95% CI, 0.43-0.99). These findings indicate that the rs4938723 in the promoter region of pri-miR-34b/c was a protective factor for the development of CRC. As the significance is marginal, further replication studies are warranted to confirm these results.

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出版当年[2013]版:
大类 | 3 区 生物
小类 | 3 区 生化与分子生物学
最新[2023]版:
大类 | 4 区 生物学
小类 | 4 区 生化与分子生物学
第一作者:
第一作者机构: [1]Key Laboratory of Obstetric and Gynecologic and Pediatric Diseases and Birth Defects of Ministry of Education , Chengdu, Sichuan 610041 , P.R. China [2]Laboratory of Molecular and Translational Medicine, West China Institute of Women and Children ’ s Health, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610041 , P.R. China
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通讯机构: [1]Key Laboratory of Obstetric and Gynecologic and Pediatric Diseases and Birth Defects of Ministry of Education , Chengdu, Sichuan 610041 , P.R. China [*1]Laboratory of Molecular and Translational Medicine , West China Institute of Women and Children ’ s Health, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610041 , P.R. China
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