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前列腺癌中的 microRNA 失调:网络分析揭示高度连接节点的优先调控。

microRNA dysregulation in prostate cancer: network analysis reveals preferential regulation of highly connected nodes.

机构信息

Doctoral Program in Integrative Life Science, Virginia Commonwealth University, P.O. Box 842030, Richmond, VA 23284, USA.

出版信息

Chem Biodivers. 2012 May;9(5):857-67. doi: 10.1002/cbdv.201100386.

DOI:10.1002/cbdv.201100386
PMID:22589088
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3386794/
Abstract

microRNAs (miRNAs) are small RNAs shown to contribute to a number of cellular processes including cell growth, differentiation, and apoptosis. MiRNAs regulate gene expression of their targets post-transcriptionally by binding to messenger RNA (mRNA), causing translational inhibition or mRNA degradation. Dysregulation of miRNA expression can promote cancer formation and progression. Research has largely focused on the function and expression of single miRNAs. However, complex physiological processes require the interaction, regulation and coordination of many molecules including miRNAs and proteins. Highly connected molecules often serve important roles in the cell. A protein-protein interaction network of established miRNA targets confirmed these proteins to be highly connected and essential to the cell, affecting tumorigenesis, cell growth/proliferation, cellular death, cell assembly, and maintenance pathways. This analysis showed that miRNAs contribute to the overall health of the prostate, and their aberrant expression destabilized homeostatic balance. This integrative network approach can reveal important miRNAs and proteins in prostate cancer that will be useful to identify specific disease biomarkers, which may be used as targets for therapeutics or drugs in themselves.

摘要

microRNAs (miRNAs) 是一种小 RNA,被证明参与了许多细胞过程,包括细胞生长、分化和凋亡。miRNAs 通过与信使 RNA(mRNA)结合,在转录后调节其靶基因的表达,从而导致翻译抑制或 mRNA 降解。miRNA 表达失调可促进癌症的形成和发展。研究主要集中在单个 miRNAs 的功能和表达上。然而,复杂的生理过程需要许多分子(包括 miRNAs 和蛋白质)的相互作用、调节和协调。高连接分子通常在细胞中发挥重要作用。已建立的 miRNA 靶蛋白的蛋白质-蛋白质相互作用网络证实了这些蛋白质具有高度的连接性和对细胞的重要性,影响肿瘤发生、细胞生长/增殖、细胞死亡、细胞组装和维持途径。该分析表明,miRNAs 有助于前列腺的整体健康,其异常表达破坏了体内平衡。这种整合网络方法可以揭示前列腺癌中重要的 miRNAs 和蛋白质,这将有助于鉴定特定的疾病生物标志物,这些生物标志物本身可能被用作治疗或药物的靶点。

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1
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2
A comparative study of cancer proteins in the human protein-protein interaction network.在人类蛋白质-蛋白质相互作用网络中比较癌症蛋白。
BMC Genomics. 2010 Dec 1;11 Suppl 3(Suppl 3):S5. doi: 10.1186/1471-2164-11-S3-S5.
3
Multiple microRNAs modulate p21Cip1/Waf1 expression by directly targeting its 3' untranslated region.
miR-125b作为肿瘤抑制因子的双重作用以及miR-22促进前列腺癌肿瘤发生
PLoS One. 2015 Nov 6;10(11):e0142373. doi: 10.1371/journal.pone.0142373. eCollection 2015.
4
A networks method for ranking microRNA dysregulation in cancer.一种用于对癌症中微小RNA失调进行排名的网络方法。
BMC Syst Biol. 2013;7 Suppl 5(Suppl 5):S3. doi: 10.1186/1752-0509-7-S5-S3. Epub 2013 Dec 9.
5
Reconstruction and analysis of transcription factor-miRNA co-regulatory feed-forward loops in human cancers using filter-wrapper feature selection.利用过滤包装特征选择法对人类癌症中转录因子 - miRNA 共调控前馈环进行重构与分析。
PLoS One. 2013 Oct 29;8(10):e78197. doi: 10.1371/journal.pone.0078197. eCollection 2013.
6
Screening biomarkers of prostate cancer by integrating microRNA and mRNA microarrays.通过整合微小RNA和信使核糖核酸微阵列筛选前列腺癌的生物标志物
Genet Test Mol Biomarkers. 2013 Nov;17(11):807-13. doi: 10.1089/gtmb.2013.0226. Epub 2013 Aug 28.
7
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8
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Pharmacol Ther. 2013 Jun;138(3):333-408. doi: 10.1016/j.pharmthera.2013.01.016. Epub 2013 Feb 4.
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4
Analyzing biological network parameters with CentiScaPe.使用 CentiScaPe 分析生物网络参数。
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7
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8
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9
The database of experimentally supported targets: a functional update of TarBase.实验支持靶点数据库:TarBase的功能更新
Nucleic Acids Res. 2009 Jan;37(Database issue):D155-8. doi: 10.1093/nar/gkn809. Epub 2008 Oct 27.
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