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将转录网络与乳腺癌生存相关联:大规模共表达分析。

Correlating transcriptional networks to breast cancer survival: a large-scale coexpression analysis.

机构信息

National Institute for Cellular Biotechnology and.

出版信息

Carcinogenesis. 2013 Oct;34(10):2300-8. doi: 10.1093/carcin/bgt208. Epub 2013 Jun 5.

Abstract

Weighted gene coexpression network analysis (WGCNA) is a powerful 'guilt-by-association'-based method to extract coexpressed groups of genes from large heterogeneous messenger RNA expression data sets. We have utilized WGCNA to identify 11 coregulated gene clusters across 2342 breast cancer samples from 13 microarray-based gene expression studies. A number of these transcriptional modules were found to be correlated to clinicopathological variables (e.g. tumor grade), survival endpoints for breast cancer as a whole (disease-free survival, distant disease-free survival and overall survival) and also its molecular subtypes (luminal A, luminal B, HER2+ and basal-like). Examples of findings arising from this work include the identification of a cluster of proliferation-related genes that when upregulated correlated to increased tumor grade and were associated with poor survival in general. The prognostic potential of novel genes, for example, ubiquitin-conjugating enzyme E2S (UBE2S) within this group was confirmed in an independent data set. In addition, gene clusters were also associated with survival for breast cancer molecular subtypes including a cluster of genes that was found to correlate with prognosis exclusively for basal-like breast cancer. The upregulation of several single genes within this coexpression cluster, for example, the potassium channel, subfamily K, member 5 (KCNK5) was associated with poor outcome for the basal-like molecular subtype. We have developed an online database to allow user-friendly access to the coexpression patterns and the survival analysis outputs uncovered in this study (available at http://glados.ucd.ie/Coexpression/).

摘要

加权基因共表达网络分析(WGCNA)是一种基于“关联即有罪”的强大方法,可从大型异质信使 RNA 表达数据集提取共表达基因群。我们利用 WGCNA 从 13 项基于微阵列的基因表达研究的 2342 个乳腺癌样本中鉴定了 11 个核心调控基因簇。这些转录模块中的许多与临床病理变量(例如肿瘤分级)、乳腺癌的总体生存终点(无病生存、无远处疾病生存和总生存)以及其分子亚型(管腔 A、管腔 B、HER2+和基底样)相关。该研究的结果包括鉴定出一组与增殖相关的基因,当这些基因上调时与肿瘤分级增加相关,并且总体上与不良预后相关。该基因簇内新基因的预后潜力,例如泛素结合酶 E2S(UBE2S),在独立数据集得到了证实。此外,基因簇还与乳腺癌分子亚型的生存相关,包括与基底样乳腺癌预后相关的基因簇。该共表达簇内的几个单个基因上调,例如钾通道亚家族 K,成员 5(KCNK5),与基底样分子亚型的不良预后相关。我们开发了一个在线数据库,以允许用户友好地访问本研究中揭示的共表达模式和生存分析结果(可在 http://glados.ucd.ie/Coexpression/ 访问)。

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