MGMT Leu84Phe polymorphism contributes to cancer susceptibility: evidence from 44 case-control studies.

BACKGROUND: O(6)-methylguanine-DNA methyltransferase is one of the few proteins to directly remove alkylating agents in the human DNA direct reversal repair pathway. A large number of case-control studies have been conducted to explore the association between MGMT Leu84Phe polymorphism and cancer ri...

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Main Authors: Jun Liu, Renxia Zhang, Fei Chen, Cuicui Yu, Yan Sun, Chuanliang Jia, Lijing Zhang, Taufiq Salahuddin, Xiaodong Li, Juntian Lang, Xicheng Song
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3784571?pdf=render
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spelling doaj-811cebd6ada34f6c8da3e31cdebdceac2020-11-25T01:34:37ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0189e7536710.1371/journal.pone.0075367MGMT Leu84Phe polymorphism contributes to cancer susceptibility: evidence from 44 case-control studies.Jun LiuRenxia ZhangFei ChenCuicui YuYan SunChuanliang JiaLijing ZhangTaufiq SalahuddinXiaodong LiJuntian LangXicheng SongBACKGROUND: O(6)-methylguanine-DNA methyltransferase is one of the few proteins to directly remove alkylating agents in the human DNA direct reversal repair pathway. A large number of case-control studies have been conducted to explore the association between MGMT Leu84Phe polymorphism and cancer risk. However, the results were not consistent. METHODS: We carried out a meta-analysis of 44 case-control studies to clarify the association between the Leu84Phe polymorphism and cancer risk. RESULTS: Overall, significant association of the T allele with cancer susceptibility was verified with meta-analysis under a recessive genetic model (P<0.001, OR=1.30, 95%CI 1.24-1.50) and TT versus CC comparison (P=0.001, OR=1.29, 95% CI 1.12-1.50). In subgroup analysis, a significant increased risk was found for lung cancer (TT versus CC, P=0.027, OR=1.67, 95% CI 1.06-2.63; recessive genetic model, P=0.32, OR=1.64, 95% CI 1.04-2.58), whereas risk of colorectal cancer was significantly low under a dominant genetic model (P=0.019, OR=0.84, 95% CI 0.72-0.97). Additionally, a significant association between TT genetic model and total cancer risk was found in the Caucasian population (TT versus CC, P=0.014, OR=1.29, 95% CI 1.05-1.59; recessive genetic model, P=0.009, OR=1.31, 95% CI 1.07-1.61), but not in the Asian population. An increased risk for lung cancer was also verified in the Caucasian population (TT versus CC, P=0.035, OR=1.62, 95% CI 1.04-2.53; recessive genetic model, P=0.048, OR=1.57, 95% CI 1.01-2.45). CONCLUSIONS: These results suggest that MGMT Leu84Phe polymorphism might contribute to the susceptibility of certain cancers.http://europepmc.org/articles/PMC3784571?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jun Liu
Renxia Zhang
Fei Chen
Cuicui Yu
Yan Sun
Chuanliang Jia
Lijing Zhang
Taufiq Salahuddin
Xiaodong Li
Juntian Lang
Xicheng Song
spellingShingle Jun Liu
Renxia Zhang
Fei Chen
Cuicui Yu
Yan Sun
Chuanliang Jia
Lijing Zhang
Taufiq Salahuddin
Xiaodong Li
Juntian Lang
Xicheng Song
MGMT Leu84Phe polymorphism contributes to cancer susceptibility: evidence from 44 case-control studies.
PLoS ONE
author_facet Jun Liu
Renxia Zhang
Fei Chen
Cuicui Yu
Yan Sun
Chuanliang Jia
Lijing Zhang
Taufiq Salahuddin
Xiaodong Li
Juntian Lang
Xicheng Song
author_sort Jun Liu
title MGMT Leu84Phe polymorphism contributes to cancer susceptibility: evidence from 44 case-control studies.
title_short MGMT Leu84Phe polymorphism contributes to cancer susceptibility: evidence from 44 case-control studies.
title_full MGMT Leu84Phe polymorphism contributes to cancer susceptibility: evidence from 44 case-control studies.
title_fullStr MGMT Leu84Phe polymorphism contributes to cancer susceptibility: evidence from 44 case-control studies.
title_full_unstemmed MGMT Leu84Phe polymorphism contributes to cancer susceptibility: evidence from 44 case-control studies.
title_sort mgmt leu84phe polymorphism contributes to cancer susceptibility: evidence from 44 case-control studies.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description BACKGROUND: O(6)-methylguanine-DNA methyltransferase is one of the few proteins to directly remove alkylating agents in the human DNA direct reversal repair pathway. A large number of case-control studies have been conducted to explore the association between MGMT Leu84Phe polymorphism and cancer risk. However, the results were not consistent. METHODS: We carried out a meta-analysis of 44 case-control studies to clarify the association between the Leu84Phe polymorphism and cancer risk. RESULTS: Overall, significant association of the T allele with cancer susceptibility was verified with meta-analysis under a recessive genetic model (P<0.001, OR=1.30, 95%CI 1.24-1.50) and TT versus CC comparison (P=0.001, OR=1.29, 95% CI 1.12-1.50). In subgroup analysis, a significant increased risk was found for lung cancer (TT versus CC, P=0.027, OR=1.67, 95% CI 1.06-2.63; recessive genetic model, P=0.32, OR=1.64, 95% CI 1.04-2.58), whereas risk of colorectal cancer was significantly low under a dominant genetic model (P=0.019, OR=0.84, 95% CI 0.72-0.97). Additionally, a significant association between TT genetic model and total cancer risk was found in the Caucasian population (TT versus CC, P=0.014, OR=1.29, 95% CI 1.05-1.59; recessive genetic model, P=0.009, OR=1.31, 95% CI 1.07-1.61), but not in the Asian population. An increased risk for lung cancer was also verified in the Caucasian population (TT versus CC, P=0.035, OR=1.62, 95% CI 1.04-2.53; recessive genetic model, P=0.048, OR=1.57, 95% CI 1.01-2.45). CONCLUSIONS: These results suggest that MGMT Leu84Phe polymorphism might contribute to the susceptibility of certain cancers.
url http://europepmc.org/articles/PMC3784571?pdf=render
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