患有侵袭性前列腺癌的波多黎各西班牙裔/拉美裔男性的 5hmC 特征。

Manishkumar S Patel, Mousa Almubarak, Jaime Matta, Carmen Ortiz-Sanchez, Jarline Encarnacion, Gilberto Ruiz-Deya, Julie Dutil, Jasreman Dhillon, Kosj Yamoah, Anders Berglund, Hyun Park, Deepak Kilari, Yoganand Balagurunathan, Liang Wang, Jong Y Park
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引用次数: 0

摘要

波多黎各(PR)西班牙裔/拉美裔(H/L)男性是一个未得到充分研究的人群,在其他西班牙裔人群中,他们的前列腺癌(PCa)死亡率最高。关于西裔/拉美裔男性死亡率较高的信息知之甚少。人们认为,关键基因的表观遗传变化可能在侵袭性肿瘤中起到关键作用。我们旨在确定患有侵袭性 PCa 的 PR H/L 男性中 5-hydroxymethylcytosine (5hmC) 的关键变化。我们使用来自 22 个前列腺肿瘤和 24 个相邻正常 FFPE 样本的 5hmC 富集 DNA 进行了测序分析。与邻近的正常组织相比,我们在肿瘤中发现了 808 个差异甲基化基因(DMGs)(FDR|0.4|)。DMGs的通路分析表明,DNA修复通路在肿瘤中上调最多。由于 5hmC 丰度与基因表达水平呈正相关,我们进一步研究了 TCGA PCa 基因表达数据中的 808 个 DMGs。此外,我们还发现了59个DMGs(80.1%,FDR|1|)具有同方向的显著基因表达变化。此外,我们还发现了111个与侵袭性相关的DMGs,其中2个低甲基化基因(CCDC122、NUDT15)和4个高甲基化基因(PVT1、RPL30、TRMT12、UBR5)在PR H/L PCa患者(N=86)中以一致的方式发生了转录组水平的改变。在混合型 PCa 患者中,这六个基因的 5hmC 异常变化(N=55)和 GE 异常变化(N=497)也与无进展生存期相关。总之,我们的研究发现了 59 个 DMGs 在肿瘤组织中显示出一致的表观遗传学和转录组变化,111 个 DMGs 在 PR H/L 男性中显示出与侵袭性 PCa 的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
5hmC-profiles in Puerto Rican Hispanic/Latino men with aggressive prostate cancer.

Puerto Rican (PR) Hispanic/Latino (H/L) men are an understudied population that has the highest prostate cancer (PCa) specific mortality among other Hispanic populations. Little information is known about the higher mortality in PR H/L men. It is thought that epigenetic changes in key genes may play a critical role in aggressive tumors. We aimed to identify key 5-hydroxymethylcytosine (5hmC) changes in PR H/L men with aggressive PCa. We performed sequencing analysis using the 5hmC-enriched DNA from 22 prostate tumors and 24 adjacent normal FFPE samples. We identified 808 differentially methylated genes (DMGs) in tumors compared to adjacent normal tissues (FDR<0.05, log2FC>|0.4|). Pathway analysis of DMGs demonstrated that DNA repair pathway was most upregulated in tumors. Since 5hmC abundance positively correlates with gene expression levels, we further investigated 808 DMGs in TCGA PCa gene expression data. Further, we identified 59 DMGs (80.1%, FDR<0.05, ΔGE (gene expression) >|1|) with significant gene expression changes in the same direction. Additionally, we identified 111 aggressiveness-related DMGs, of which, two hypomethylated genes ( CCDC122 , NUDT15 ) and four hypermethylated genes ( PVT1 , RPL30 , TRMT12 , UBR5 ) were found to be altered at transcriptomic level in a concordant manner in PR H/L PCa patients (N=86). The aberrant 5hmC (N=55) and GE (N=497) changes in these six genes were also associated with progression-free survival in the mixed PCa population. In conclusion, our study identified 59 DMGs showing concordant epigenetic and transcriptomic changes in tumor tissues and 111 DMGs showing association with aggressive PCa among PR H/L men.

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