Genome-wide association analysis reveals regulation of at-risk loci by DNA methylation in prostate cancer

• 作者: Qiang Liu Gang Liu Darryl T Martin Yu-Tong Xing Robert M Weiss Jun Qi Jian Kang
• 来源期刊: 亚洲男性学杂志（英文版）
• 年，卷（期）: 2021,（5）
• 所属期刊栏目: ORIGINAL ARTICLE
• 页码范围: 472-478
• 页数: 7页
• 语种: 英文
• DOI: 10.4103/aja.aja_20_21

摘要

Epigenetic changes are potentially important for the ontogeny and progression of tumors but are not usually studied because of the complexity of analyzing transcript regulation resulting from epigenetic alterations.Prostate cancer(PCa)is characterized by variable clinical manifestations and frequently unpredictable outcomes.We performed an expression quantitative trait loci(eQTL)analysis to identify the genomic regions that regulate gene expression in PCa and identified a relationship between DNA methylation and clinical information.Using multi-level information published in The Cancer Genome Atlas,we performed eQTL-based analyses on DNA methylation and gene expression.To better interpret these data,we correlated loci and clinical indexes to identify the important loci for both PCa development and progression.Our data demonstrated that although only a small proportion of genes are regulated via DNA methylation in PCa,these genes are enriched in important cancer-related groups.In addition,single nucleotide polymorphism analysis identified the locations of CpG sites and genes within at-risk loci,including the 19q13.2-q13.43 and 16q22.2-q23.1 loci.Further,an epigenetic association study of clinical indexes detected risk loci and pyrosequencing for site validation.Although DNA methylation-regulated genes across PCa samples are a small proportion,the associated genes play important roles in PCa carcinogenesis.