The hMLH1 promoter polymorphisms and cancer susceptibility in Asian populations: A meta-analysis

被引:5
作者
He, Yuanzhou [1 ]
Xu, Xiangqin [1 ]
Chen, Huilong [1 ]
Wang, Jianmiao [1 ]
Xiong, Weining [1 ]
Xu, Yongjian [1 ]
Liu, Jin [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Minist Hlth, Dept Resp Dis,Tongji Hosp,Key Lab Pulm Dis, Wuhan 430030, Peoples R China
关键词
hMLH1; Polymorphisms; Meta-analysis; Cancer; Asian populations; DNA MISMATCH REPAIR; SINGLE-NUCLEOTIDE POLYMORPHISM; LUNG-CANCER; COLORECTAL-CANCER; MICROSATELLITE INSTABILITY; GASTRIC CARCINOMAS; GENE; RISK; ASSOCIATION; METHYLATION;
D O I
10.1016/j.gene.2013.03.138
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: A variety of studies have evaluated the associations between polymorphisms in the promoter regions of the hMLH1 and cancer risk. However, the results remain inconclusive. To better understand the roles of the hMLH1 polymorphisms and cancer risk, we conducted a comprehensive meta-analysis to investigate the association between the hMLH1 -93G/A and 1151T/A (Val384Asp) polymorphisms and cancer risk in Asian population. Methods: We performed a meta-analysis by conducting searches of the published studies in Pub Med, CNKI, CBM, ISI web of knowledge and Google scholar search databases. Finally, 12 studies were included into our meta-analysis. Overall and subgroup analyses were performed. Odds ratio (OR) and 95% confidence interval (Cl) were used to evaluate the associations between hMLH1 polymorphisms and cancer risk. Statistical analysis was performed with Review Manager 5.0. Results: Twelve studies addressing two hMLH1 polymorphisms were analyzed among a total of 4128 cancer cases and 4678 controls. For hMLH1 -93G/A, there was no evidence that the hMLH1 -93G/A polymorphism was significantly associated with an increased cancer risk (P > 0.05) in Asian populations (heterozygote comparison: OR = 0.89 [95% CI (0.75, 1.060)] P = 0.20; dominant model comparison: OR = 0.98 [95% CI (0.83, 1.15)] P = 0.79). In subgroup analysis based on cancer types and the sources of control, no associations were found in colorectal cancer, gastric cancer and "other cancers" under the any gene model except for lung cancer (recessive model comparison: OR = 1.69 [95% CI (1.30, 2.19)] P < 0.0001). For hMLH1 1151T/A, the polymorphism significantly associated with an increased cancer risk in Asians: OR = 1.88 [95% CI (1.49, 2.25)], P < 0.0001, and OR = 1.87 [95% CI (1.49, 2.25)], P < 0.0001. Conclusions: Our investigations demonstrated that the hMLH1 -93G/A polymorphism is not a candidate for susceptibility to overall cancers, and that the hMLH1 1151T/A polymorphism is significantly associated with higher cancer risk in Asian populations. Further studies with large sample size for hMLH1 should be conducted. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:199 / 204
页数:6
相关论文
共 43 条
[1]   Polymorphisms in hMLH1 and risk of early-onset lung cancer in a southeast Chinese population [J].
An, Yu ;
Jin, Guangfu ;
Wang, Haifeng ;
Wang, Yi ;
Liu, Hongliang ;
Li, Rui ;
Wang, Haijian ;
Qian, Ji ;
Sun, Weiwei ;
Wang, Yi ;
Ma, Hongxia ;
Miao, Ruifeng ;
Hu, Zhibin ;
Jin, Li ;
Wei, Qingyi ;
Shen, Hongbing ;
Huang, Wei ;
Lu, Daru .
LUNG CANCER, 2008, 59 (02) :164-170
[2]   Molecular pathogenesis of colorectal cancer - Implications for molecular diagnosis [J].
Arnold, CN ;
Goel, A ;
Blum, HE ;
Boland, CR .
CANCER, 2005, 104 (10) :2035-2047
[3]   Functional interactions and signaling properties of mammalian DNA mismatch repair proteins [J].
Bellacosa, A .
CELL DEATH AND DIFFERENTIATION, 2001, 8 (11) :1076-1092
[4]   Characterization of the interactome of the human MutL homologues MLH1, PMS1, and PMS2 [J].
Cannavo, Elda ;
Gerrits, Bertran ;
Marra, Giancarlo ;
Schlapbach, Ralph ;
Jiricny, Josef .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (05) :2976-2986
[5]   Methylation-induced G2/M arrest requires a full complement of the mismatch repair protein hMLH1 [J].
Cejka, P ;
Stojic, L ;
Mojas, N ;
Russell, AM ;
Heinimann, K ;
Cannavó, E ;
di Pietro, M ;
Marra, G ;
Jiricny, J .
EMBO JOURNAL, 2003, 22 (09) :2245-2254
[6]   Genetic Variations in Esophageal Cancer Risk and Prognosis [J].
Cheung, Winson Y. ;
Liu, Geoffrey .
GASTROENTEROLOGY CLINICS OF NORTH AMERICA, 2009, 38 (01) :75-+
[7]   Silencing-specific methylation and single nucleotide polymorphism of hMLH1 promoter in gastric carcinomas [J].
Deng, DJ ;
Zhou, J ;
Zhu, BD ;
Ji, JF ;
Harper, JC ;
Powell, SM .
WORLD JOURNAL OF GASTROENTEROLOGY, 2003, 9 (01) :26-29
[8]  
Fleisher AS, 1999, CANCER RES, V59, P1090
[9]   DNA binding by yeast Mlh1 and Pms1: implications for DNA mismatch repair [J].
Hall, MC ;
Shcherbakova, PV ;
Fortune, JM ;
Borchers, CH ;
Dial, JM ;
Tomer, KB ;
Kunkel, TA .
NUCLEIC ACIDS RESEARCH, 2003, 31 (08) :2025-2034
[10]   Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma [J].
Herman, JG ;
Umar, A ;
Polyak, K ;
Graff, JR ;
Ahuja, N ;
Issa, JPJ ;
Markowitz, S ;
Willson, JKV ;
Hamilton, SR ;
Kinzler, KW ;
Kane, MF ;
Kolodner, RD ;
Vogelstein, B ;
Kunkel, TA ;
Baylin, SB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (12) :6870-6875