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YWHAZ 和 NDRG1 的表达可预测人类前列腺癌的侵袭性结局。

The expression of YWHAZ and NDRG1 predicts aggressive outcome in human prostate cancer.

机构信息

Laboratorio de Inflamación y Cáncer, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, C1428EGA, Argentina.

Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales (IQUIBICEN), CONICET-Universidad de Buenos Aires, Buenos Aires, C1428EGA, Argentina.

出版信息

Commun Biol. 2021 Jan 22;4(1):103. doi: 10.1038/s42003-020-01645-2.

Abstract

Some prostate cancers (PCas) are histo-pathologically grouped within the same Gleason Grade (GG), but can differ significantly in outcome. Herein, we aimed at identifying molecular biomarkers that could improve risk prediction in PCa. LC ESI-MS/MS was performed on human PCa and benign prostatic hyperplasia (BPH) tissues and peptide data was integrated with omic analyses. We identified high YWHAZ and NDRG1 expression to be associated with poor PCa prognosis considering all Gleason scores (GS). YWHAZ and NDRG1 defined two subpopulations of PCa patients with high and intermediate risk of death. Multivariable analyses confirmed their independence from GS. ROC analysis unveiled that YWHAZ outperformed GS beyond 60 months post-diagnosis. The genomic analysis of PCa patients with YWHAZ amplification, or increased mRNA or protein levels, revealed significant alterations in key DNA repair genes. We hereby state the relevance of YWHAZ in PCa, showcasing its role as an independent strong predictor of aggressiveness.

摘要

一些前列腺癌(PCa)在组织病理学上被归入相同的 Gleason 分级(GG)中,但在预后上可能存在显著差异。在此,我们旨在确定分子生物标志物,以改善 PCa 的风险预测。对人前列腺癌和良性前列腺增生(BPH)组织进行 LC ESI-MS/MS 分析,并整合肽数据与组学分析。我们发现,考虑到所有 Gleason 评分(GS),高 YWHAZ 和 NDRG1 表达与 PCa 预后不良相关。YWHAZ 和 NDRG1 定义了两个具有高和中等死亡风险的 PCa 患者亚群。多变量分析证实了它们与 GS 的独立性。ROC 分析显示,在诊断后 60 个月以上,YWHAZ 优于 GS。对 YWHAZ 扩增或 mRNA 或蛋白水平升高的 PCa 患者的基因组分析显示,关键 DNA 修复基因发生了显著改变。我们在此声明 YWHAZ 在 PCa 中的相关性,展示了其作为侵袭性的独立强预测因子的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27a4/7822895/45fb73567894/42003_2020_1645_Fig1_HTML.jpg

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