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CENPF和NDC80在肝细胞癌和肝硬化康复护理中的作用:一项观察性研究。

Role of CENPF and NDC80 in the rehabilitation nursing of hepatocellular carcinoma and cirrhosis: An observational study.

作者信息

Jia Wei, Wu Qiaoling, Li Ruipu, Hou Shiyang, Kang Chunbo

机构信息

Gastrointestinal Rehabilitation Center, Beijing Rehabilitation Hospital, Capital Medical University, Shijingshan District, Beijing, P.R. China.

出版信息

Medicine (Baltimore). 2024 May 3;103(18):e37984. doi: 10.1097/MD.0000000000037984.

Abstract

Hepatocellular carcinoma (HCC) is one of the most common malignant tumors globally and often develops on the foundation of chronic liver disease or cirrhosis. Cirrhosis is a clinically prevalent chronic progressive liver disease characterized by diffuse liver damage resulting from long-term or repeated actions of 1 or more etiological factors. However, the impact of CENPF and nuclear division cycle 80 (NDC80) genes on rehabilitation nursing of HCC and cirrhosis remains unclear. HCC and cirrhosis datasets GSE63898 and GSE89377 profile files were downloaded from the gene expression omnibus database generated on platforms GPL13667 and GPL6947, respectively. Differentially expressed genes (DEGs) screening, weighted gene co-expression network analysis (WGCNA), construction and analysis of protein-protein interaction (PPI) networks, functional enrichment analysis, gene set enrichment analysis (GSEA), survival analysis, immune infiltration analysis, and comparative toxicogenomics database (CTD) analysis were conducted. Gene expression heatmaps were plotted. miRNAs regulating central DEGs were selected through TargetScan. A total of 626 DEGs were identified. According to gene ontology (GO) analysis, they were primarily enriched in small molecule metabolic processes, drug metabolic processes, binding of identical proteins, and lipid metabolic processes. Kyoto Encyclopedia of Gene and Genome (KEGG) analysis results indicated that the target genes were mainly enriched in metabolic pathways, phagosomes, glycine, serine, and threonine metabolism. The construction and analysis of the PPI network revealed 3 core genes (NDC80, CENPF, RRM2). Gene expression heatmaps showed that core genes (CENPF, NDC80) were highly expressed in HCC and cirrhosis samples. CTD analysis found that 2 genes (CENPF and NDC80) were associated with liver, jaundice, ascites, fever, dyspepsia, and hepatic encephalopathy. CENPF and NDC80 are highly expressed in HCC and cirrhosis, and CENPF and NDC80 might be the biomarkers of rehabilitation nursing of HCC and cirrhosis.

摘要

肝细胞癌(HCC)是全球最常见的恶性肿瘤之一,通常在慢性肝病或肝硬化的基础上发展而来。肝硬化是一种临床上普遍存在的慢性进行性肝病,其特征是由一种或多种病因长期或反复作用导致的弥漫性肝损伤。然而,着丝粒蛋白F(CENPF)和核分裂周期80(NDC80)基因对HCC和肝硬化康复护理的影响仍不清楚。分别从在平台GPL13667和GPL6947上生成的基因表达综合数据库中下载了HCC和肝硬化数据集GSE63898和GSE89377的配置文件。进行了差异表达基因(DEG)筛选、加权基因共表达网络分析(WGCNA)、蛋白质-蛋白质相互作用(PPI)网络的构建和分析、功能富集分析、基因集富集分析(GSEA)、生存分析、免疫浸润分析以及比较毒理基因组学数据库(CTD)分析。绘制了基因表达热图。通过TargetScan选择调控核心DEG的微小RNA(miRNA)。共鉴定出626个DEG。根据基因本体(GO)分析,它们主要富集于小分子代谢过程、药物代谢过程、相同蛋白质的结合以及脂质代谢过程。京都基因与基因组百科全书(KEGG)分析结果表明,靶基因主要富集于代谢途径、吞噬体、甘氨酸、丝氨酸和苏氨酸代谢。PPI网络的构建和分析揭示了3个核心基因(NDC80、CENPF、RRM2)。基因表达热图显示,核心基因(CENPF、NDC80)在HCC和肝硬化样本中高表达。CTD分析发现,2个基因(CENPF和NDC80)与肝脏、黄疸、腹水、发热、消化不良和肝性脑病有关。CENPF和NDC80在HCC和肝硬化中高表达,CENPF和NDC80可能是HCC和肝硬化康复护理的生物标志物。

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