MTHFR C677T polymorphism and anatomopathological characteristics with prognostic significance in sporadic colorectal cancer

2015 ◽  
Vol 211 (12) ◽  
pp. 989-995
Author(s):  
Luciano Delgado-Plasencia ◽  
Hugo Álvarez-Argüelles ◽  
Eduardo Salido-Ruiz ◽  
M. Elisa Castro-Peraza ◽  
Alberto Bravo-Gutiérrez ◽  
...  
2012 ◽  
Vol 95 (2) ◽  
pp. 405-412 ◽  
Author(s):  
Jeongseon Kim ◽  
Young Ae Cho ◽  
Dong-Hyun Kim ◽  
Bong-Hwa Lee ◽  
Dae-Yong Hwang ◽  
...  

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.


2012 ◽  
Vol 39 (10) ◽  
pp. 9669-9679 ◽  
Author(s):  
Xuewen Sheng ◽  
Yanxi Zhang ◽  
Erjiang Zhao ◽  
Su Lu ◽  
Xiaoli Zheng ◽  
...  

2013 ◽  
Vol 28 (9) ◽  
pp. 1187-1193 ◽  
Author(s):  
Luciano Delgado-Plasencia ◽  
Vicente Medina-Arana ◽  
Alberto Bravo-Gutiérrez ◽  
Julián Pérez-Palma ◽  
Hugo Álvarez-Argüelles ◽  
...  

2020 ◽  
Vol 19 (1) ◽  
pp. 209-213
Author(s):  
Yong-lian Zhang ◽  
Xiong-wei Xie

Purpose: To investigate the toxicity of methylenetetrahydrofolate reductase (MTHFR) polymorphism in colorectal cancer patients treated with 5-fluorouracil (5-FU).Methods: A total of 105 patients with colorectal cancer who underwent 5-FU therapy were included in this study. MTHFR C677T polymorphisms were determined using direct sequencing. Physical examination and the results of blood and urine tests were used to evaluate the toxicities, including gastrointestinal toxicity, hematopoietic toxicity, hair-skin toxicity and hand-foot syndrome.Results: In 90.5 % of all patients, 5-FU toxicity was observed. With regard to MTHFR C677T mutation, 45.7 % heterozygote mutants and 19.0 % homozygote mutants were observed. MTHFR C677T polymorphism was statistically related to 5-FU toxicity (p = 0.000). In addition, MTHFR C677T mutation was closely related to hematopoietic toxicity (p = 0.005).Conclusion: MTHFR C677T can be used for the prediction of 5-FU toxicity, and can also predict hematopoietic toxicity in patients with colorectal cancer. Keywords: MTHFR genes, Polymorphism, Colorectal cancer, Biomarker, Toxicity


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