Fernandez Pedro, Salie Muneeb, du Toit Danielle, van der Merwe Andre
Division of Urology and Tygerberg Hospital, Stellenbosch University, P.O. Box 241, Cape Town 8000, South Africa.
SA MRC Centre for TB Research and DST/NRF Centre of Excellence for Biomedical Tuberculosis Research, Division of Molecular Biology and Human Genetics, Stellenbosch University, P.O. Box 241, Cape Town 8000, South Africa.
Prostate Cancer. 2015;2015:465184. doi: 10.1155/2015/465184. Epub 2015 Aug 12.
Genome-wide association studies (GWAS) have implicated single nucleotide polymorphisms (SNPs) on chromosomes 2p15, 6q25, 7p15.2, 7q21, 8q24, 10q11, 10q26, 11q13, 17q12, 17q24, 19q13, and Xp11, with prostate cancer (PCa) susceptibility and/or tumour aggressiveness, in populations of African, European, and Asian ancestry. The objective of this study was to confirm these associations in South African Mixed Ancestry and White men. We evaluated 17 prioritised GWAS SNPs in South African cases (331 Mixed Ancestry and 155 White) and controls (178 Mixed Ancestry and 145 White). The replicated SNP associations for the different South African ethnic groups were rs7008482 (8q24) (p = 2.45 × 10(-5)), rs6983267 (8q24) (p = 4.48 × 10(-7)), and rs10993994 (10q11) (p = 1.40 × 10(-3)) in Mixed Ancestry men and rs10993994 (p = 1.56 × 10(-9)) in White men. No significant associations were observed for the analyses stratified by disease aggressiveness in the individual and the combined population group analysis. The present study demonstrates that a number of known PCa susceptibility variants may contribute to disease susceptibility in South African men. Larger genetic investigations extended to other South African population groups are warranted to confirm the role of these and other SNPs in disease susceptibility.
全基因组关联研究(GWAS)已表明,在非洲、欧洲和亚洲血统人群中,位于染色体2p15、6q25、7p15.2、7q21、8q24、10q11、10q26、11q13、17q12、17q24、19q13和Xp11上的单核苷酸多态性(SNP)与前列腺癌(PCa)易感性和/或肿瘤侵袭性有关。本研究的目的是在南非混血和白人男性中证实这些关联。我们评估了南非病例(331名混血和155名白人)和对照(178名混血和145名白人)中的17个优先GWAS SNP。不同南非种族群体中重复的SNP关联在混血男性中为rs7008482(8q24)(p = 2.45×10⁻⁵)、rs6983267(8q24)(p = 4.48×10⁻⁷)和rs10993994(10q11)(p = 1.40×10⁻³),在白人男性中为rs10993994(p = 1.56×10⁻⁹)。在个体和合并人群组分析中,按疾病侵袭性分层的分析未观察到显著关联。本研究表明,一些已知的PCa易感性变异可能导致南非男性的疾病易感性。有必要对更多南非人群组进行更大规模的基因研究,以确认这些和其他SNP在疾病易感性中的作用。