DNA repair polymorphisms XRCC1 and MGMT and risk of adult gliomas

被引:59
|
作者
Felini, Martha J.
Olshan, Andrew F.
Schroeder, Jane C.
North, Kari E.
Carozza, Susan E.
Kelsey, Karl T.
Liu, Mei
Rice, Terri
Wiencke, John K.
Wrensch, Margaret R.
机构
[1] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC USA
[2] Texas A&M Univ, Ctr Hlth Sci, Dept Epidemiol, College Stn, TX USA
[3] Univ Calif San Francisco, Dept Neurol Surg & Epidemiol & Biostat, San Francisco, CA 94143 USA
[4] Harvard Univ, Sch Publ Hlth, Dept Genet & Complex Dis, Boston, MA 02115 USA
关键词
gliomas; brain tumors; DNA repair polymorphisms; XRCC1; MGMT; case-control;
D O I
10.1159/000108919
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
X-ray cross complementing group 1 (XRCC1) and O6- methylguanineDNA methyltransferase (MGMT) are pivotal repair genes focused on repairing lesions due to ionizing radiation, alkylating agents, and oxidative DNA damage, risk factors previously linked to gliomas. Using the population based San Francisco Adult Glioma study, we evaluated associations between XRCC1 Arg399Gln, MGMT Leu84Phe, and MGMT Ile143Val polymorphisms with glioma risk among white cases (n = 441 to 453) and controls (n = 487 to 526). We found no evidence of an association between XRCC1 genotypes and glioma. We observed a weak positive association for the MGMT Leu84Phe polymorphism (Leu or Phe/Phe versus Leu/Leu: adjusted OR = 1.26; CI 0.90 - 1.75) and the MGMT Ile143Val polymorphism ( Ile or Val/ Val versus IIe/ IIe: adjusted OR = 1.20; CI 0.85 - 1.71). Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:55 / 58
页数:4
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