Impact of Mir196a-2 Genotypes on Colorectal Cancer Risk in Taiwan

被引:9
|
作者
Yueh, Te-Cheng [1 ,2 ,3 ]
Wang, Yun-Chi [3 ,4 ]
Chin, Yu-Ting [3 ,4 ]
Hung, Yi-Chih [3 ,4 ]
Mong, Mei-Chin [5 ]
Yang, Ya-Chen [5 ]
Pei, Jen-Sheng [6 ]
Gu, Jian [7 ]
Tsai, Chia-Wen [3 ,4 ,7 ]
Bau, Da-Tian [3 ,4 ,8 ]
Chang, Wen-Shin [3 ,4 ,7 ]
机构
[1] Taichung Armed Forces Gen Hosp, Dept Surg, Div Colon & Rectal Surg, Taichung 41152, Taiwan
[2] Natl Def Med Ctr, Taipei 11490, Taiwan
[3] China Med Univ, Grad Inst Biomed Sci, Taichung 404333, Taiwan
[4] China Med Univ Hosp, Dept Med Res, Terry Fox Canc Res Lab, Taichung 404327, Taiwan
[5] Asia Univ, Dept Food Nutr & Hlth Biotechnol, Taichung 41354, Taiwan
[6] Taoyuan Gen Hosp, Dept Pediat, Minist Hlth & Welf, Taoyuan 33004, Taiwan
[7] Univ Texas MD Anderson Canc Ctr, Dept Epidemiol, Houston, TX 77030 USA
[8] Asia Univ, Dept Bioinformat & Med Engn, Taichung 41354, Taiwan
关键词
colorectal cancer; genotype; mir146a; mir196a-2; phenotype; polymorphism; GENETIC-VARIANTS; SUSCEPTIBILITY; ASSOCIATION; POLYMORPHISM; MIR-146A; MICRORNA-196A2; SURVIVAL; POPULATION; MIR-196-A2; MIRNA;
D O I
10.3390/ijms241411613
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
We aimed to investigate the association between genotypes for mir146a and mir196a-2 and the risk of developing colorectal cancer (CRC). We used polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) to determine the mir146a rs2910164 and mir196a-2 rs11614913 genotypes in 362 CRC patients and 362 controls. We also assessed the interactions between these genotypes and age, gender, smoking, alcohol consumption, and BMI status on CRC risk. Additionally, the serum expression level of mir196a-2 was quantified using quantitative reverse transcription-PCR. Our findings demonstrated that among the controls, the proportions of TT, CT, and CC genotypes of mir196a-2 rs11614913 were 32.3%, 48.1%, and 19.6%, respectively. As for the cases, the proportions were 24.6%, 45.0%, and 30.4%, respectively. Logistic regression analysis revealed that the CC genotype carriers had a 2.04-fold increased risk (95% confidence interval [CI] = 1.36-3.06, p = 0.0008). Furthermore, carriers of the CT + CC genotypes also exhibited a significant association with CRC risk (odds ratio [OR] = 1.46, 95% CI = 1.06-2.03, p = 0.0261). Moreover, carriers of the CC genotype had significantly higher serum levels of mir196a-2 compared to those with the TT genotype (p < 0.0001), indicating a genotype-phenotype correlation. No association was found regarding mir146a rs2910164. In conclusion, mir196a-2 rs2910164 genotypes, along with their associated expression, can serve as predictive markers for CRC risk.
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收藏
页数:12
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