Analysis of the role of POC1A in the development and progression of hepatocellular carcinoma.

IF 1.5 4区 医学 Q4 ONCOLOGY
Translational cancer research Pub Date : 2024-09-30 Epub Date: 2024-09-27 DOI:10.21037/tcr-23-2398
Hongrui Zhou, Mengxue Zhang, Xin Zhang, Xintong Du, Huihui Cao, Xiuli Bi
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引用次数: 0

Abstract

Background: Hepatocellular carcinoma (HCC) is one of the most common and deadly cancers worldwide. POC1 centriolar protein A (POC1A) is a gene encoding a protein that plays a key role in the centrosome, and is one of the two isoforms of POC1. To date, the expression of POC1A in HCC and its potential as a biomarker and tumor therapeutic target have not been examined. This study aimed to explore the effect of POC1A on patients with HCC and its potential mechanism.

Methods: This study investigated the role of POC1A in the occurrence and development of HCC. It analyzed the expression of POC1A in various types of HCC patients and its effect on survival using HCC patient information from the Gene Expression Omnibus (GEO), The Cancer Genome Atlas (TCGA), the Human Protein Atlas (HPA), and the Hepatocellular Carcinoma Cell DataBase (HCCDB). It then explored the major enrichment pathways and gene functions of POC1A in HCC using the gene set enrichment analysis (GSEA) method and examined its protein-protein interactions (PPIs). Finally, it predicted the potential transcription factors (TFs) and target microRNAs (miRNAs) of POC1A, and analyzed the single nucleotide variation (SNV) and copy number variation (CNV) mutations of POC1A and the related genes in HCC, as well as their effects on immune cells.

Results: The results showed that POC1A was significantly overexpressed in HCC and was significantly associated with a poor prognosis. The Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses indicated that POC1A was mainly involved in the regulation of cell-cycle pathways and chromosome segregation functions. POC1A showed significant interactions with NUDC and PPARG, and they both had different numbers of SNV and CNV mutations in the HCC samples. In relation to immunity, the high expression of POC1A and its reciprocal genes may play an important role in B cells and macrophages.

Conclusions: In general, our findings suggest that POC1A overexpression could have an important effect on the development of HCC by regulating cell-cycle pathways, and that it could serve as a novel prognostic biomarker and a potential therapeutic target for HCC.

分析 POC1A 在肝细胞癌的发生和发展中的作用。
背景:肝细胞癌(HCC肝细胞癌(HCC)是全球最常见、最致命的癌症之一。POC1 中心体蛋白 A(POC1A)是一种编码在中心体中发挥关键作用的蛋白质的基因,也是 POC1 的两种异构体之一。迄今为止,尚未研究 POC1A 在 HCC 中的表达及其作为生物标志物和肿瘤治疗靶点的潜力。本研究旨在探讨 POC1A 对 HCC 患者的影响及其潜在机制:本研究探讨了 POC1A 在 HCC 发生和发展中的作用。研究利用基因表达总库(GEO)、癌症基因组图谱(TCGA)、人类蛋白质图谱(HPA)和肝细胞癌细胞数据库(HCCDB)中的HCC患者信息,分析了POC1A在不同类型HCC患者中的表达及其对生存的影响。然后利用基因组富集分析(GSEA)方法探讨了POC1A在HCC中的主要富集途径和基因功能,并研究了其蛋白-蛋白相互作用(PPIs)。最后,研究人员预测了POC1A的潜在转录因子(TFs)和靶microRNAs(miRNAs),分析了POC1A及相关基因在HCC中的单核苷酸变异(SNV)和拷贝数变异(CNV)突变及其对免疫细胞的影响:结果表明,POC1A在HCC中明显过表达,且与预后不良明显相关。基因本体(GO)和京都基因组百科全书(KEGG)分析表明,POC1A 主要参与细胞周期通路和染色体分离功能的调控。POC1A与NUDC和PPARG有明显的相互作用,在HCC样本中,它们都有不同数量的SNV和CNV突变。在免疫方面,POC1A及其互作基因的高表达可能在B细胞和巨噬细胞中发挥重要作用:总之,我们的研究结果表明,POC1A的过表达可能通过调节细胞周期通路对HCC的发展产生重要影响,它可以作为一种新的预后生物标志物和HCC的潜在治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
252
期刊介绍: Translational Cancer Research (Transl Cancer Res TCR; Print ISSN: 2218-676X; Online ISSN 2219-6803; http://tcr.amegroups.com/) is an Open Access, peer-reviewed journal, indexed in Science Citation Index Expanded (SCIE). TCR publishes laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer; results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of cancer patients. The focus of TCR is original, peer-reviewed, science-based research that successfully advances clinical medicine toward the goal of improving patients'' quality of life. The editors and an international advisory group of scientists and clinician-scientists as well as other experts will hold TCR articles to the high-quality standards. We accept Original Articles as well as Review Articles, Editorials and Brief Articles.
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