Associations between hsa-miR-603 polymorphism, lifestyle-related factors and colorectal cancer risk

被引:20
|
作者
Wang, Fen-Juan [1 ]
Ding, Ye [2 ]
Mao, Ying-Ying [2 ]
Jing, Fang-Yuan [2 ]
Zhang, Zhen-Yu [2 ]
Jiang, Long-Fang [1 ]
Guo, Jian-Feng [1 ]
Sun, Xiang-Jue [1 ]
Jin, Ming-Juan [2 ]
Chen, Kun [2 ]
机构
[1] Ctr Dis Control & Prevent Xiaoshan, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, Hangzhou 310058, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
hsa-miR-603; polymorphism; colorectal cancer; susceptibility; CELL LUNG-CANCER; TEA CONSUMPTION; MICRORNA; EXPRESSION; SUPPRESSES; BIOMARKERS; MECHANISM; MIGRATION; INVASION; PROFILE;
D O I
10.3233/CBM-140395
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Accumulated studies have suggested that single nucleotide polymorphisms (SNPs) in microRNAs are associated with risk of colorectal cancer (CRC). OBJECTIVE: We tested our hypothesis that rs11014002 in hsa-miR-603 may be associated with CRC risk with a crosstalk of life-related factors. METHODS: We conducted a case-control study which included 102 CRC patients and 204 matched cancer-free controls in Xiaoshan County. RESULTS: We observed that subjects with rs11014002 CT/TT genotype had an increased susceptibility for CRC (CT vs. CC: odds ratio (OR) = 2.352, 95% confidence interval (CI): 1.142-4.840, P = 0.020; CT+TT vs. CC: OR = 2.031, 95% CI: 1.063-3.883, P = 0.032). After stratification by lifestyle-related factors, similar results were found among nonsmokers (CT vs. CC: OR = 2.753, 95% CI: 1.085-6.983, P = 0.033; CT+TT vs. CC: OR = 2.971, 95% CI: 1.188-7.435, P = 0.020) and non-alcohol drinkers (CT+TT vs. CC: OR = 3.279, 95% CI: 1.071-10.033, P = 0.037). CONCLUSIONS: Our data suggest that hsa-miR-603 may be involved in colorectal tumorigenesis, and the genetic polymorphism in hsa-miR-603 is associated with CRC susceptibility.
引用
收藏
页码:225 / 231
页数:7
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