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首页> 外文期刊>Cancer investigation >Co-Expression Network Analysis Identified Genes Associated with Cancer Stem Cell Characteristics in Lung Squamous Cell Carcinoma
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Co-Expression Network Analysis Identified Genes Associated with Cancer Stem Cell Characteristics in Lung Squamous Cell Carcinoma

机译:共表达网络分析鉴定了肺鳞状细胞癌中癌症干细胞特征相关的基因

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Objective: Cancer stem cells are self-renewal cells in tumors and can produce heterogeneous tumor cells, which play an important role in the development of lung squamous cell carcinoma (LSCC). In our research, we aimed to explore the expression of genes related to LSCC stem cells. Methods: We downloaded the RNAseq data, the pathological and prognostic profiles of LSCC cases from the public database TCGA. The mRNA expression-based stiffness index (mRNAsi) of LSCC was calculated and the prognostic value of mRNAsi was discussed. Then, we constructed a weighted gene co-expression network analysis (WGCNA) to screen key genes related to mRNAsi of LSCC. Results: MRNAsi is an independent prognostic factor in LSCC. We screened 5 key genes (BUB1, BIRC5, CCNB2, KIF15 and SPAG5) related to mRNAsi of LSCC based on WGCNA. The key genes were highly expressed in the tumor samples compared to the normal samples. In addition, there is a strong interaction between proteins of these key genes and a strong co-expression relationship at the transcriptional level. Conclusions: To conclude, mRNAsi play an important role in LSCC. Five key genes (BUB1, BIRC5, CCNB2, KIF15 and SPAG5) related to mRNAsi were screened, which may act as therapeutic targets for inhibiting the stem cell characteristics of LSCC.
机译:目的:肿瘤干细胞是肿瘤中自我更新的细胞,能产生异质性肿瘤细胞,在肺鳞状细胞癌(LSCC)的发生发展中起重要作用。在我们的研究中,我们旨在探索LSCC干细胞相关基因的表达。方法:我们从公共数据库TCGA下载RNAseq数据、LSCC病例的病理和预后资料。计算LSCC的基于mRNA表达的僵硬指数(mRNAsi),并讨论其预后价值。然后,我们构建了加权基因共表达网络分析(WGCNA)来筛选与LSCC mRNAsi相关的关键基因。结果:MRNAsi是LSCC的独立预后因素。我们根据WGCNA筛选了与LSCC mRNAsi相关的5个关键基因(BUB1、BIRC5、CCNB2、KIF15和SPAG5)。与正常样本相比,关键基因在肿瘤样本中高度表达。此外,这些关键基因的蛋白质之间存在强烈的相互作用,并且在转录水平上存在强烈的共表达关系。结论:总之,mRNAsi在LSCC中起着重要作用。筛选出5个与mRNAsi相关的关键基因(BUB1、BIRC5、CCNB2、KIF15和SPAG5),它们可能作为抑制LSCC干细胞特性的治疗靶点。

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