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Application of microRNA and mRNA expression profiling on prognostic biomarker discovery for hepatocellular carcinoma

机译:MicroRNA和mRNA表达分析在肝细胞癌预后生物标志物发现中的应用

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Background: Hepatocellular carcinoma (HCC) is one of the most highly malignant and lethal cancers of the world. Its pathogenesis has been reported to be multi-factorial, and the molecular carcinogenesis of HCC can not be attributed to just a few individual genes. Based on the microRNA and mRNA expression profiling of normal liver tissues, pericancerous hepatocellular tissues and hepatocellular carcinoma tissues, we attempted to find prognosis related gene sets for HCC patients. Results: We identified differentially expressed genes (DEG) from three comparisons: Cancer/Normal, Cancer/ Pericancerous and Pericancerous/Normal. GSEA (gene set enrichment analysis) were performed. Based on the enriched gene sets of GO terms, pathways and transcription factor targets, it was found that the genome instability and cell proliferation increased while the metabolism and differentiation decreased in HCC tissues. The expression profile of DEGs in each enriched gene set was used to correlate to the postoperative survival time of HCC patients. Nine gene sets were found to prognostic correlation. Furthermore, after substituting DEG-targeting-microRNA for DEG members of each gene set, two gene sets with the microRNA expression profiles were obtained that had prognostic potential. Conclusions: The malignancy of HCC could be represented by gene sets, and pericancerous liver exhibits important characteristics of liver cancer. The expression level of gene sets not only in HCC but also in the pericancerous liver showed potential for prognosis implying an option for HCC prognosis at an early stage. Additionally, the gene-targeting-microRNA expression profiles also showed prognostic potential, demonstrating that the multi-factorial molecular pathogenesis of HCC is contributed by various genes and microRNAs.
机译:背景:肝细胞癌(HCC)是世界上最高度恶性和致死的癌症之一。据报道,其发病机制是多因素的,并且HCC的分子致癌物质不能归因于少数个体基因。基于正常肝组织的microRNA和mRNA表达分析,术语肝细胞癌和肝细胞癌组织,我们试图寻找HCC患者的预后相关基因套。结果:我们从三个比较中鉴定了差异表达的基因(DEG):癌症/正常,癌症/卵巢癌症和眼经古典/正常。 GSEA(基因集富集分析)进行了。基于富集的基因组的GO术语,途径和转录因子靶标,发现基因组不稳定性和细胞增殖在HCC组织中降低了代谢和分化。每种富集基因集合中的DEG的表达谱用于与HCC患者的术后存活时间相关。发现九种基因集预后相关性。此外,在用每个基因组的DEG构件代替DEG靶向微小RORNA之后,获得了具有预后潜力的微小RNA表达谱的两个基因组。结论:HCC的恶性肿瘤可由基因套代表,卵巢肝脏表现出肝癌的重要特征。基因的表达水平不仅在HCC中,而且在卵巢血症中表现出预后的潜力,这意味着在早期阶段的HCC预后的选择。另外,基因靶向微润松表达谱还显示出预后潜力,证明HCC的多因素分子发病机制由各种基因和微大罗氏产生贡献。

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