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Meta-analysis of gene expression studies in endometrial cancer identifies gene expression profiles associated with aggressive disease and patient outcome

机译:子宫内膜癌基因表达研究的荟萃分析可确定与侵袭性疾病和患者预后相关的基因表达谱

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Although endometrioid endometrial cancer (EEC; comprising ~80% of all endometrial cancers diagnosed) is typically associated with favourable patient outcome, a significant portion (~20%) of women with this subtype will relapse. We hypothesised that gene expression predictors of the more aggressive non-endometrioid endometrial cancers (NEEC) could be used to predict EEC patients with poor prognosis. To explore this hypothesis, we performed meta-analysis of 12 gene expression microarray studies followed by validation using RNA-Seq data from The Cancer Genome Atlas (TCGA) and identified 1,253 genes differentially expressed between EEC and NEEC. Analysis found 121 genes were associated with poor outcome among EEC patients. Forward selection likelihood-based modelling identified a 9-gene signature associated with EEC outcome in our discovery RNA-Seq dataset which remained significant after adjustment for clinical covariates, but was not significant in a smaller RNA-Seq dataset. Our study demonstrates the value of employing meta-analysis to improve the power of gene expression microarray data, and highlight genes and molecular pathways of importance for endometrial cancer therapy.
机译:尽管子宫内膜样子宫内膜癌(EEC;占诊断出的所有子宫内膜癌的80%)通常与患者良好的预后相关,但这种亚型的女性中有相当一部分(〜20%)会复发。我们假设更具侵略性的非子宫内膜样子宫内膜癌(NEEC)的基因表达预测因子可用于预测预后较差的EEC患者。为了探索这一假设,我们对12个基因表达微阵列研究进行了荟萃分析,然后使用来自癌症基因组图谱(TCGA)的RNA-Seq数据进行验证,并鉴定了1,253个在EEC和NEEC之间差异表达的基因。分析发现121个基因与EEC患者的不良预后相关。基于正向选择似然性的模型在我们的发现RNA-Seq数据集中确定了与EEC结果相关的9基因签名,在对临床协变量进行调整后,该基因仍然显着,而在较小的RNA-Seq数据集中则没有显着性。我们的研究证明了采用荟萃分析提高基因表达微阵列数据的能力的价值,并突出了对子宫内膜癌治疗重要的基因和分子途径。

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