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Bioinformatics analysis of gene expression profile of serous ovarian carcinomas to screen key genes and pathways

机译:浆液癌基因表达谱对筛选关键基因和途径的生物信息分析

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BACKGROUND:Serous ovarian carcinomas (SCA) are the most common and most aggressive ovarian carcinoma subtype which etiology remains unclear. To investigate the prospective role of mRNAs in the tumorigenesis and progression of SCA, the aberrantly expressed mRNAs were calculated based on the NCBI-GEO RNA-seq data.RESULTS:Of 21,755 genes with 89 SCA and SBOT cases from 3 independent laboratories, 59 mRNAs were identified as differentially expressed genes (DEGs) (|logsub2/subFold Change| ?1.585, also |FoldChange| ?3 and adjusted P??0.05) by DESeq R. There were 26 up-regulated DEGs and 33 down-regulated DEGs screened. The hierarchical clustering analysis, functional analysis and pathway enrichment analysis were performed on all DEGs and found that Polo-like kinase (PLK) signaling events are important. PPI network constructed with different filtration conditions screened out 4 common hub genes (KIF11, CDC20, PBK and TOP2A). Mutual exclusivity or co-occurrence analysis of 4 hub genes identified a tendency towards co-occurrence between KIF11 and CDC20 or TOP2A in SCA (p??0.05). To analyze further the potential role of KIF11 in SCA, the co-expression profiles of KIF11 in SCA were identified and we found that CDC20 co-expressed with KIF11 also is DEG that we screened out before. To verify our previous results in this paper, we assessed the expression levels of 4 hub DEGs (all up-regulated) and 4 down-regulated DEGs in Oncomine database. And the results were consistent with previous conclusions obtained from GEO series. The survival curves showed that KIF11, CDC20 and TOP2A expression are significantly related to prognosis of SCA patients.CONCLUSIONS:From all the above results, we speculate that KIF11, CDC20 and TOP2A played an important role in SCA.
机译:背景:浆液卵巢癌(SCA)是最常见,最具侵略性的卵巢癌亚型,其病因尚不清楚。为了探讨MRNA在SCA肿瘤发生和进展中的前瞻性作用,基于NCBI-Geo RNA-SEQ数据计算异常表达的MRNA。结果:来自3个独立实验室的89个SCA和SBOT病例的21,755个基因,59 mRNA被鉴定为差异表达的基因(Degs)(| log 2 折叠变化|>β1.585,也|折叠|>?3并调整p?<0.05),并在其中有26个 - 筛选的DEG和33个下调的次数。在所有次数上进行分层聚类分析,功能分析和途径富集分析,发现Polo样激酶(PLK)信号传导事件很重要。用不同的过滤条件构建的PPI网络筛选出4个常见的轮毂基因(KIF11,CDC20,PBK和TOP2A)。 4个枢纽基因的互速性或共生发生分析确定了KIF11和CDC20或SCA中TOP2A之间共发生的趋势(P?<?0.05)。为了进一步分析KIF11在SCA中的潜在作用,鉴定了KIF11在SCA中的共表达谱,并发现CDC20与KIF11共同表达也是我们之前筛选的DEG。要验证我们以前的结果,我们评估了Oncommate数据库中的4个集线器(全部监管)和4个下调的次数的表达水平。结果与先前从Geo系列获得的结论一致。存活曲线表明,KIF11,CDC20和TOP2A表达与SCA患者的预后显着相关。结论:来自所有上述结果,我们推测KIF11,CDC20和TOP2A在SCA中发挥着重要作用。

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