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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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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