期刊
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE
卷 105, 期 8, 页码 573-579出版社
OXFORD UNIV PRESS INC
DOI: 10.1093/jnci/djt018
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资金
- US National Institutes of Health [R01CA137013, R01CA148667, R01CA124558, R01CA064277, R37CA070867, R01CA118229, R01CA092585, R01CA122756]
- Ingram Professorship and Research Reward funds
- Department of Defense (DOD) Idea Awards [BC011118, BC050791]
- Vanderbilt-Ingram Cancer Center [P30 CA68485]
- Cancer Research UK [12011] Funding Source: researchfish
Genome-wide association studies (GWASs) have identified multiple genetic susceptibility loci for breast cancer. However, these loci explain only a small fraction of the heritability. Very few studies have evaluated copy number variation (CNV), another important source of human genetic variation, in relation to breast cancer risk. We conducted a CNV GWAS in 2623 breast cancer patients and 1946 control subjects using data from Affymetrix SNP Array 6.0 (stage 1). We then replicated the most promising CNV using real-time quantitative polymerase chain reaction (qPCR) in an independent set of 4254 case patients and 4387 control subjects (stage 2). All subjects were recruited from population-based studies conducted among Chinese women in Shanghai. Of the 268 common CNVs (minor allele frequency 5%) investigated in stage 1, the strongest association was found for a common deletion in the APOBEC3 genes (P 1.110(4)) and was replicated in stage 2 (odds ratio 1.35, 95% confidence interval [CI] 1.27 to 1.44; P 9.610(22)). Analyses of all samples from both stages using qPCR data produced odds ratios of 1.31 (95% CI 1.21 to 1.42) for a one-copy deletion and 1.76 (95% CI 1.57 to 1.97) for a two-copy deletion (P 2.010(24)). We provide convincing evidence for a novel breast cancer locus at the APOBEC3 genes. This CNV is one of the strongest common genetic risk variants identified so far for breast cancer.
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