Cheng Siyuan, Yu Xiuping
Department of Biochemistry and Molecular Biology, LSU Health-Shreveport Shreveport, USA.
Am J Clin Exp Urol. 2019 Oct 15;7(5):327-340. eCollection 2019.
Gene expression profiles are valuable resources for the identification of key players that driver disease progression. However, neuroendocrine prostate cancer (NEPCa) specimens are rare, limiting research on this aggressive disease. In this study, we generated a 12-gene signature of NEPCa and used this signature to differentiate NEPCa from prostate adenocarcinoma (AdPCa) samples in publicly available datasets. From these samples, we identified genes that were differentially expressed in NEPCa and AdPCa. Gene ontology and network analyses revealed key players in the pathogenesis of NEPCa, including E2Fs, members of MHC class II, and factors involved in neuron differentiation, neurogenesis, and stem cell signaling. In conclusion, we identified a 12-gene signature of NEPCa and found pathways that are important for the pathologic development of NEPCa.
基因表达谱是识别驱动疾病进展的关键因素的宝贵资源。然而,神经内分泌前列腺癌(NEPCa)标本稀少,限制了对这种侵袭性疾病的研究。在本研究中,我们生成了NEPCa的12基因特征,并使用该特征在公开可用的数据集中区分NEPCa和前列腺腺癌(AdPCa)样本。从这些样本中,我们鉴定出在NEPCa和AdPCa中差异表达的基因。基因本体论和网络分析揭示了NEPCa发病机制中的关键因素,包括E2F、MHC II类成员以及参与神经元分化、神经发生和干细胞信号传导的因子。总之,我们鉴定出了NEPCa的12基因特征,并发现了对NEPCa病理发展重要的通路。