Lin Hui-Yi, Wang Xinnan, Tseng Tung-Sung, Kao Yu-Hsiang, Fang Zhide, Molina Patricia E, Cheng Chia-Ho, Berglund Anders E, Eeles Rosalind A, Muir Kenneth R, Pashayan Nora, Haiman Christopher A, Brenner Hermann, Consortium The Practical, Park Jong Y
Biostatistics Program, School of Public Health, Louisiana State University Health Sciences Center, New Orleans, LA 70112, USA.
Behavioral and Community Health Sciences Program, School of Public Health, Louisiana State University Health Sciences Center, New Orleans, LA 70112, USA.
J Clin Med. 2021 Feb 2;10(3):553. doi: 10.3390/jcm10030553.
Excessive alcohol intake is a well-known modifiable risk factor for many cancers. It is still unclear whether genetic variants or single nucleotide polymorphisms (SNPs) can modify alcohol intake's impact on prostate cancer (PCa) aggressiveness. The objective is to test the alcohol-SNP interactions of the 7501 SNPs in the four pathways (angiogenesis, mitochondria, miRNA, and androgen metabolism-related pathways) associated with PCa aggressiveness. We evaluated the impacts of three excessive alcohol intake behaviors in 3306 PCa patients with European ancestry from the PCa Consortium. We tested the alcohol-SNP interactions using logistic models with the discovery-validation study design. All three excessive alcohol intake behaviors were not significantly associated with PCa aggressiveness. However, the interactions of excessive alcohol intake and three SNPs (rs13107662 [, = 6.2 × 10], rs9907521 [ = 7.1 × 10], and rs11925452 [ = 8.2 × 10]) were significantly associated with PCa aggressiveness. These alcohol-SNP interactions revealed contrasting effects of excessive alcohol intake on PCa aggressiveness according to the genotypes in the identified SNPs. We identified PCa patients with the rs13107662 () AA genotype, the rs11925452 () AA genotype, and the rs9907521 ( AG genotype were more vulnerable to excessive alcohol intake for developing aggressive PCa. Our findings support that the impact of excessive alcohol intake on PCa aggressiveness was varied by the selected genetic profiles.
过量饮酒是许多癌症已知的可改变风险因素。基因变异或单核苷酸多态性(SNP)是否能改变饮酒对前列腺癌(PCa)侵袭性的影响仍不清楚。目的是测试与PCa侵袭性相关的四个途径(血管生成、线粒体、miRNA和雄激素代谢相关途径)中7501个SNP的酒精-SNP相互作用。我们评估了来自PCa联盟的3306名欧洲血统PCa患者的三种过量饮酒行为的影响。我们使用发现-验证研究设计的逻辑模型测试了酒精-SNP相互作用。所有三种过量饮酒行为均与PCa侵袭性无显著关联。然而,过量饮酒与三个SNP(rs13107662 [, = 6.2 × 10]、rs9907521 [ = 7.1 × 10]和rs11925452 [ = 8.2 × 10])的相互作用与PCa侵袭性显著相关。这些酒精-SNP相互作用揭示了根据所识别SNP中的基因型,过量饮酒对PCa侵袭性的不同影响。我们确定携带rs13107662()AA基因型、rs11925452()AA基因型和rs9907521(AG基因型的PCa患者更容易因过量饮酒而发展为侵袭性PCa。我们的研究结果支持过量饮酒对PCa侵袭性的影响因所选基因谱而异。