scholarly journals Genetic variants in 3′-UTRs of methylenetetrahydrofolate reductase (MTHFR) predict colorectal cancer susceptibility in Koreans

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Young Joo Jeon ◽  
Jong Woo Kim ◽  
Hye Mi Park ◽  
Jung O Kim ◽  
Hyo Geun Jang ◽  
...  
PLoS ONE ◽  
2012 ◽  
Vol 7 (7) ◽  
pp. e41954 ◽  
Author(s):  
Janelle M. Hoskins ◽  
Pei-Shi Ong ◽  
Temitope O. Keku ◽  
Joseph A. Galanko ◽  
Christopher F. Martin ◽  
...  

The Lancet ◽  
2016 ◽  
Vol 387 ◽  
pp. S102
Author(s):  
Peter G Vaughan-Shaw ◽  
Graeme Grimes ◽  
Anna-Maria Ochocka ◽  
Karen Dunbar ◽  
Maria Timofeeva ◽  
...  

2017 ◽  
Vol 37 (6) ◽  
Author(s):  
Lingyan Xu ◽  
Zhiqiang Qin ◽  
Feng Wang ◽  
Shuhui Si ◽  
Lele Li ◽  
...  

The association between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and colorectal cancer (CRC) susceptibility has been researched in numerous studies. However, the results of these studies were controversial. Therefore, the objective of this meta-analysis was to offer a more convincible conclusion about such association with more included studies. Eligible studies published till May 1, 2017 were searched from PubMed, Embase, Web of Science, and CNKI database about such association. Pooled odds ratios (ORs) together with 95% confidence intervals (CIs) were calculated to evaluate such association. And the Begg’s funnel plot and Egger’s test were applied to assess the publication bias. This meta-analysis contained 37049 cases and 52444 controls from 87 publications with 91 eligible case–control studies. Because of lack of data for a particular genotype in several studies, all the included studies were analysed barely in the dominant model. Originally, there was no association between MTHFR C677T polymorphism and CRC susceptibility (OR =0.99, 95% CI =0.94–1.05). After excluding 13 studies according to their heterogeneity and publication bias, rs1801133 polymorphism was found to reduce the risks of CRC significantly (OR =0.96, 95% CI =0.94–0.99). In the subgroup analysis of ethnicity, there was a significant association in Asians (OR =0.94, 95% CI =0.89–1.00). Furthermore, when stratified by the source of controls and genotyping methods, the positive results were observed in population-based control group (OR =0.97, 95% CI =0.93–1.00) and PCR-restriction fragment length polymorphism (PCR-RFLP) method (OR =0.95, 95% CI =0.91–0.99. The results of the meta-analysis suggested that MTHFR C677T polymorphism was associated with CRC susceptibility, especially in Asian population.


2020 ◽  
Vol 2020 ◽  
pp. 1-5 ◽  
Author(s):  
Zhi-Gang Gao ◽  
Yong Yang ◽  
Xiao-Feng Han ◽  
Yun-Lei Wang ◽  
Zhen-Jun Wang

Colorectal cancer (CRC) is the 5th leading cancer in China. Alcohol consumption has been reported to be one of the risk factors of CRC. However, it remains unclear whether genetic variants of alcohol metabolic genes are associated with CRC risk. In this study, we tested the coding variants in the alcohol metabolic genes and the risk of CRC, by using 485 cases and 516 controls. A total of 16 germline coding variants in 10 alcohol metabolic genes were genotyped. We identified that rs3741178 in ALDH3B2 was significantly associated with CRC risk with odds ratio being 2.13 (95% CI: 1.24–3.68, P=0.0064). Further functional annotation suggested that this variant may damage the protein function of ALDH3B2. Our results suggested that ALDH3B2 in the alcohol metabolism pathway contributed to the development of CRC, which may contribute to the prevention of this disease in the future.


2020 ◽  
Vol 10 ◽  
Author(s):  
Jung Oh Kim ◽  
Hak Hoon Jun ◽  
Eo Jin Kim ◽  
Jeong Yong Lee ◽  
Han Sung Park ◽  
...  

2013 ◽  
Vol 133 (10) ◽  
pp. 2325-2333 ◽  
Author(s):  
Shun Lu ◽  
Melanie Bevier ◽  
Stefanie Huhn ◽  
Juan Sainz ◽  
Jesus Lascorz ◽  
...  

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