Genotype GG of rs895819 Functional Polymorphism Within miR-27a Might Increase Genetic Susceptibility to Colorectal Cancer in Han Chinese Population

被引:20
|
作者
Jiang, Yu [1 ]
Lin, Dong-Hong [2 ]
Xu, Jian-Ping [2 ]
Chen, Wen-XU [1 ]
Zheng, Shu-Jian [3 ]
Song, Lin [3 ]
机构
[1] Xiamen Univ, Fuzhou Hosp 2, Dept Clin Lab, Fuzhou, Fujian, Peoples R China
[2] Fujian Med Univ, Dept Clin Lab Med, 88 Jiao Tong Rd, Taijiang 350004, Fuzhou, Peoples R China
[3] Xiamen Univ, Fuzhou Hosp 2, Oncol Surg, Fuzhou, Fujian, Peoples R China
关键词
colorectal cancer; polymorphism; rs895819; ONCOGENIC MICRORNA-27A; MESENCHYMAL TRANSITION; DRUG-RESISTANCE; ASSOCIATION; CELLS; PROLIFERATION; EXPRESSION; VARIANT; RISK; METASTASIS;
D O I
10.1002/jcla.21862
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BackgroundMicroRNA-27a (miR-27a) is supposed to be an oncogene in various types of cancers, and genetic variation of miR-27a might result in aberrant expression and abnormal second structure of mature-miR-27a, contributing to elevated genetic risk and poor prognosis for colorectal cancer (CRC). MethodsIn order to explore the possible association between rs895819 within miR-27a and CRC in Han Chinese population, we investigated the genotype distributions of rs895819 in 508 CRC cases and 562 healthy check-up controls using TaqMan genotype discrimination system, and analyzed the possible association between them. Odds ratio (OR) and 95% confidential interval (95% CI) were used to assess the strength between allele and genotype of the locus and risk of CRC. ResultsIn our study, we found that genotype GG of rs895819 was significantly associated with an increased risk for CRC (17.1% vs. 11.6%, adjusted OR = 1.546, 95% CI = 1.070-2.236), and allele A carrier (AA/AG) was significantly associated with a decreased risk for CRC (82.9% vs. 89.4%, adjusted OR = 0.63, 95% CI = 0.446-0.893). In addition, a significant association was observed between genotype GG and larger tumor size (>5 cm; P < 0.001), and allele G was significantly associated with higher pathological stage (TNM-III) (P = 0.008). ConclusionThese results indicated that miR-27a might be involved in the development and progression of CRC, genotype GG within rs895819 might be a genetic susceptible factor for CRC. Further multicentral, large sample size, and well-designed epidemiological study as well as functional study are warrant to verify our findings.
引用
收藏
页码:351 / 355
页数:5
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