A Common Deletion in the APOBEC3 Genes and Breast Cancer Risk

作者：Long Jirong^*; Delahanty Ryan J; Li Guoliang; Gao Yu Tang; Lu Wei; Cai Qiuyin; Xiang Yong Bing; Li Chun; Ji Bu Tian; Zheng Ying; Ali Simak; Shu Xiao Ou; Zheng Wei

来源：JNCI-Journal of the National Cancer Institute, 2013, 105(8): 573-579.

DOI：10.1093/jnci/djt018

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.

• 出版日期2013-4
• 单位上海市肿瘤研究所; 上海市疾病预防控制中心