Department of Biology and Center for Cancer Research, Tuskegee University, Tuskegee, AL 36088.
Pharmacology and Therapeutics, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263.
Front Biosci (Landmark Ed). 2017 Jan 1;22(2):212-229. doi: 10.2741/4482.
African Americans (AAs) who have PCa typically have more aggressive disease and make up a disproportionate number of the disease deaths, relative to European Americans (EAs). TMPRSS2 translocations, a common event in EA patients, are exploited in diagnostic and prognostic settings, whereas they are diminished in frequency in AA men. Thus, these patients with TMPRSS2 fusion-negative disease represent an under-investigated patient group. We propose that epigenetic events are a significant and alternative driver of aggressive disease in fusion-negative PCa. To reveal epigenetically governed microRNAs (miRNAs) that are enriched in fusion-negative disease and associated with aggressive in AA PCa, we leveraged both our experimental evidence and publically available data. These analyses identified 18 miRNAs that are differentially altered in fusion-negative disease, associated with DNA CpG methylation, and implicated in aggressive and AA PCas. Understanding the relationships between miRNA expression, upstream epigenetic regulation by DNA methylation, and downstream regulation of mRNA targets in fusion negative disease is imperative to understanding the biological basis of the racial health disparity in PCa.
非裔美国人(African Americans,AAs)患有前列腺癌时,疾病通常更为侵袭性,且在疾病死亡人数方面占比不成比例,与欧洲裔美国人(European Americans,EAs)相比。TMPRSS2 易位在 EA 患者中较为常见,在诊断和预后方面得到了利用,而在 AA 男性中其发生频率降低。因此,这些 TMPRSS2 融合阴性疾病患者代表了一个研究不足的患者群体。我们提出,表观遗传事件是融合阴性前列腺癌中侵袭性疾病的一个重要替代驱动因素。为了揭示在融合阴性前列腺癌中富含于融合阴性疾病并与 AA 前列腺癌侵袭性相关的受表观遗传调控的 microRNAs(miRNAs),我们利用了我们的实验证据和公开可用的数据。这些分析确定了 18 个在融合阴性疾病中差异表达的 miRNA,这些 miRNA 与 DNA CpG 甲基化相关,并与侵袭性和 AA 前列腺癌相关。了解 miRNA 表达、DNA 甲基化的上游表观遗传调控以及融合阴性疾病中 mRNA 靶标的下游调控之间的关系,对于理解前列腺癌中种族健康差异的生物学基础至关重要。