Genetic Variants of GPX1 and SOD2 and Breast Cancer Risk at the Ontario Site of the Breast Cancer Family Registry

There are several genes that code for enzymes, including various forms of superoxide dismutase and glutathione peroxidase, that protect the cell against oxidative damage that, in turn, can lead to carcinogenesis. There are a few common genetic polymorphisms in these genes that lead to altered proteins. Three that have been identified are SOD2 Val-9Ala, GPX1 Pro198Leu, and the GPX1 GCG repeat (three alleles with four, five, or six repeats). The SOD2 variant has been associated with increased breast cancer risk in two studies. The GPX1 variants have not been studied with respect to breast cancer, but Pro198Leu has been associated with lung cancer. We conducted a case-control study of these three polymorphisms in incident, invasive breast cancer in Caucasian women under 55. There were 399 cases and 372 controls genotyped, of whom 488 were premenopausal, 208 postmenopausal, and 75 of unknown menopausal status. We were unable to replicate the previously observed association with SOD2 Val-9Ala and also found no association between breast cancer and GPX1 Pro198Leu. However, the allele of GPX1 containing four GCG repeats was significantly associated with breast cancer risk in premenopausal women (odds ratio, 1.55; 95% confidence interval, 1.04–2.30 for carriers versus noncarriers). There is a significant trend of increasing risk with increasing number of alleles with four GCG repeats (P = 0.03). This variant has not previously been reported to be associated with breast cancer.

[1]  I. Andrulis,et al.  Ethnicity, but not cancer family history, is related to response to a population-based mailed questionnaire. , 2004, Annals of epidemiology.

[2]  N. Boyd,et al.  Characteristics associated with participation at various stages at the Ontario site of the cooperative family registry for breast cancer studies. , 2002, Annals of epidemiology.

[3]  R. Eeles,et al.  Association between the GCG polymorphism of the selenium dependent GPX1 gene and the risk of young onset prostate cancer , 2002, Prostate Cancer and Prostatic Diseases.

[4]  V. Kosma,et al.  Association between manganese superoxide dismutase (MnSOD) gene polymorphism and breast cancer risk. , 2001, Carcinogenesis.

[5]  D. Albanes,et al.  Glutathione peroxidase codon 198 polymorphism variant increases lung cancer risk. , 2000, Cancer research.

[6]  N. Rothman,et al.  Population stratification in epidemiologic studies of common genetic variants and cancer: quantification of bias. , 2000, Journal of the National Cancer Institute.

[7]  E. Bowman,et al.  Manganese superoxide dismutase (MnSOD) genetic polymorphisms, dietary antioxidants, and risk of breast cancer. , 1999, Cancer research.

[8]  U. Faire,et al.  Low yield of polymorphisms from EST blast searching: Analysis of genes related to oxidative stress and verification of the P197L polymorphism in GPX1 , 1999, Human mutation.

[9]  S. Loft,et al.  Cancer risk and oxidative DNA damage in man , 1997, Journal of Molecular Medicine.

[10]  Y. Mizuno,et al.  Structural dimorphism in the mitochondrial targeting sequence in the human manganese superoxide dismutase gene. A predictive evidence for conformational change to influence mitochondrial transport and a study of allelic association in Parkinson's disease. , 1996, Biochemical and biophysical research communications.

[11]  A. Junod,et al.  Role of oxygen free radicals in cancer development. , 1996, European journal of cancer.

[12]  J. Gnarra,et al.  Loss of heterozygosity of the human cytosolic glutathione peroxidase I gene in lung cancer. , 1994, Carcinogenesis.

[13]  P. Cerutti Oxy-radicals and cancer , 1994, The Lancet.

[14]  P. Newburger,et al.  An in-frame trinucleotide repeat in the coding region of the human cellular glutathione peroxidase (GPX1) gene: in vivo polymorphism and in vitro instability. , 1994, Genomics.

[15]  B. Ames,et al.  Oxidants, antioxidants, and the degenerative diseases of aging. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[16]  K. Guyton,et al.  Oxidative mechanisms in carcinogenesis. , 1993, British medical bulletin.

[17]  A. Davison,et al.  Mitochondrial mutations may increase oxidative stress: implications for carcinogenesis and aging? , 1990, Free radical biology & medicine.