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本文引用的文献

1
ShinyGO: a graphical gene-set enrichment tool for animals and plants.ShinyGO:一个用于动植物的图形基因集富集工具。
Bioinformatics. 2020 Apr 15;36(8):2628-2629. doi: 10.1093/bioinformatics/btz931.
2
Next-generation characterization of the Cancer Cell Line Encyclopedia.下一代癌症细胞系百科全书的特征描述。
Nature. 2019 May;569(7757):503-508. doi: 10.1038/s41586-019-1186-3. Epub 2019 May 8.
3
Cancer statistics, 2019.癌症统计数据,2019 年。
CA Cancer J Clin. 2019 Jan;69(1):7-34. doi: 10.3322/caac.21551. Epub 2019 Jan 8.
4
STRING v11: protein-protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets.STRING v11:具有增强覆盖范围的蛋白质-蛋白质相互作用网络,支持在全基因组实验数据集的功能发现。
Nucleic Acids Res. 2019 Jan 8;47(D1):D607-D613. doi: 10.1093/nar/gky1131.
5
SRRM4 gene expression correlates with neuroendocrine prostate cancer.SRRM4基因表达与神经内分泌前列腺癌相关。
Prostate. 2019 Jan;79(1):96-104. doi: 10.1002/pros.23715. Epub 2018 Aug 28.
6
Insulinoma-associated protein 1 is a novel sensitive and specific marker for small cell carcinoma of the prostate.胰岛素瘤相关蛋白 1 是前列腺小细胞癌一种新型的敏感且特异的标志物。
Hum Pathol. 2018 Sep;79:151-159. doi: 10.1016/j.humpath.2018.05.014. Epub 2018 Jun 6.
7
The Potential of Targeting Brain Pathology with Ascl1/Mash1.通过Ascl1/Mash1靶向脑病理学的潜力
Cells. 2017 Aug 23;6(3):26. doi: 10.3390/cells6030026.
8
HOXB13 mutations and binding partners in prostate development and cancer: Function, clinical significance, and future directions.HOXB13突变及在前列腺发育和癌症中的结合伴侣:功能、临床意义及未来方向
Genes Dis. 2017 Jun;4(2):75-87. doi: 10.1016/j.gendis.2017.01.003. Epub 2017 Feb 16.
9
Rb1 and Trp53 cooperate to suppress prostate cancer lineage plasticity, metastasis, and antiandrogen resistance.Rb1和Trp53协同作用以抑制前列腺癌的谱系可塑性、转移和抗雄激素耐药性。
Science. 2017 Jan 6;355(6320):78-83. doi: 10.1126/science.aah4199.
10
SRRM4 Drives Neuroendocrine Transdifferentiation of Prostate Adenocarcinoma Under Androgen Receptor Pathway Inhibition.SRRM4 驱动前列腺腺癌在雄激素受体通路抑制下的神经内分泌转化。
Eur Urol. 2017 Jan;71(1):68-78. doi: 10.1016/j.eururo.2016.04.028. Epub 2016 May 11.

对公开可用的神经内分泌前列腺癌(NEPCa)数据集进行生物信息学分析。

Bioinformatics analyses of publicly available NEPCa datasets.

作者信息

Cheng Siyuan, Yu Xiuping

机构信息

Department of Biochemistry and Molecular Biology, LSU Health-Shreveport Shreveport, USA.

出版信息

Am J Clin Exp Urol. 2019 Oct 15;7(5):327-340. eCollection 2019.

PMID:31763364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6872473/
Abstract

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.

摘要

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。