Oncotarget

Meta-Analysis:

Relevance of methylenetetrahydrofolate reductase gene variants C677T and A1298C with response to fluoropyrimidine-based chemotherapy in colorectal cancer: a systematic review and meta-analysis

Lei Zhong, Xia He, Yuan Zhang, Jun-Lan Chuan, Min Chen, Shao-Min Zhu and Qian Peng _

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Oncotarget. 2018; 9:31291-31301. https://doi.org/10.18632/oncotarget.24933

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Abstract

Lei Zhong1, Xia He1, Yuan Zhang1, Jun-Lan Chuan1, Min Chen1, Shao-Min Zhu2 and Qian Peng3

1Personalized Drug Therapy Key Laboratory of Sichuan Province, Hospital of the University of Electronic Science and Technology of China and Sichuan Provincial People’s Hospital, Sichuan 610072, China

2Department of Anesthesiology, East Ward, Sichuan Academy of Medical Sciences and Sichuan Provincial People’s Hospital, Sichuan 610072, China

3Cancer Center, Sichuan Academy of Medical Sciences and Sichuan Provincial People’s Hospital, Sichuan 610072, China

Correspondence to:

Qian Peng, email: pengqian0522@163.com

Shao-Min Zhu, email: 541300362@qq.com

Keywords: MTHFR; fluoropyrimidine; chemotherapy response; meta-analysis; polymorphism

Received: January 21, 2017     Accepted: March 06, 2018     Published: July 27, 2018

ABSTRACT

Methylenetetrahydrofolate reductase (MTHFR) is a critical enzyme influencing the metabolism of fluoropyrimidines. The relevance of MTHFR polymorphisms with the clinical response to fluoropyrimidine-based chemotherapy has been explored, but the results remain controversial. Thus, a meta-analysis was performed to provide a comprehensive estimate in this account. Relevant studies were identified through PubMed, Embase and Web of Science databases from inception up to May 2017. Odds ratios (ORs) with corresponding 95% confidence intervals (CIs) were applied to assess the strength of association. A total of 2118 colorectal cancer patients from 21 studies were included in the meta-analysis. Overall, there was no significant association between MTHFR C677T (rs1801133) or A1298C (rs1801131) polymorphisms and the clinical response to fluoropyrimidine-based chemotherapy under all of the three genetic models (allele model, dominant model, and recessive model) and stratification analysis, except for the retrospective study subgroup in the dominant model of MTHFR C677T and the “5-Fu + FA” treatment group in the allele contrast of MTHFR A1298C. No or moderate heterogeneity was observed in all genetic models. This meta-analysis suggested that MTHFR polymorphisms could not be considered as reliable factors for predicting the clinical response to fluoropyrimidine-based chemotherapy in colorectal cancer patients.


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