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A Functional Variant at miR-520a Binding Site in PIK3CA Alters Susceptibility to Colorectal Cancer in a Chinese Han Population

机译:PIK3CA中miR-520a结合位点的功能变异改变了中国汉族人群对大肠癌的易感性

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摘要

An increasing body of evidence has indicated that polymorphisms in the miRNA binding site of target gene can alter the ability of miRNAs to bind their target genes and modulate the risk of cancer. We aimed to investigate the association between a miR-520a binding site polymorphism rs141178472 in the PIK3CA 3′-UTR and the risk of colorectal cancer (CRC) in a Chinese Han population. The polymorphism rs141178472 was analyzed in a case-control study, including 386 CRC patients and 394 age- and sex-matched controls; the relationship between the polymorphism and the risk of colorectal cancer was examined. Individuals carrying the rs141178472 CC genotype or C allele had an increased risk of developing CRC (CC versus TT, OR (95% CI): 1.716 (1.084–2.716), P = 0.022; C versus T, OR (95% CI): 1.258 (1.021–1.551), P = 0.033). Furthermore, the expression of PIK3CA was detected in the peripheral blood mononucleated cell of CRC patients, suggesting that mRNA levels of PIK3CA might be associated with SNP rs141178472. These findings provide evidence that a miR-520a binding site polymorphism rs141178472 in the PIK3CA 3′-UTR may play a role in the etiology of CRC.
机译:越来越多的证据表明,靶基因的miRNA结合位点的多态性可以改变miRNA结合其靶基因的能力,并调节患癌症的风险。我们旨在调查中国汉族人群中PIK3CA 3'-UTR中miR-520a结合位点多态性rs141178472与结直肠癌(CRC)风险之间的关系。一项病例对照研究分析了rs141178472的多态性,包括386名CRC患者和394名年龄和性别匹配的对照。研究了多态性与大肠癌风险之间的关系。携带rs141178472 CC基因型或C等位基因的个体发生CRC的风险增加(CC与TT,OR(95%CI):1.716(1.084–2.716),P = 0.022; C与T,OR(95%CI): 1.258(1.021–1.551),P = 0.033)。此外,在CRC患者的外周血单核细胞中检测到PIK3CA的表达,表明PIK3CA的mRNA水平可能与SNP rs141178472有关。这些发现提供了PIK3CA 3'-UTR中的miR-520a结合位点多态性rs141178472的证据可能在CRC的病因中起作用。

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