基于综合分析的 SKA2 及其 ceRNA 网络在肝细胞癌中的致癌作用

IF 1.5 4区 医学 Q4 ONCOLOGY Translational cancer research Pub Date : 2024-10-31 Epub Date: 2024-10-29 DOI:10.21037/tcr-24-833
Wanxue Hu, Xiaoyi Hu, Yongchao Zhu, Min Li, Hongyu Meng, Hongbo Zhao
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引用次数: 0

摘要

背景:基因改变在癌症的发生和发展中起着重要作用。SKA2(纺锤体和动点相关复合物亚基 2)是一种有丝分裂成分,在维持分裂板和纺锤体检查点的沉默方面发挥着关键作用。然而,SKA2在肝细胞癌(HCC)中的确切作用仍不清楚。本研究旨在全面确定SKA2在HCC中的功能:我们利用各种数据库和生物信息学工具,如癌症基因组图谱(TCGA)、survminer软件包、肿瘤免疫估算资源(TIMER)、cBioPortal网站、clusterProfiler软件包、基因组富集分析(GSEA)、miRWalk、TargetScanHuman8.0、miRDB、DIANA和Cytoscape,来确定SKA2在HCC中的作用:结果:我们的研究结果表明,HCC 患者表现出 SKA2 的高表达。此外,SKA2高表达组的总生存率(OS)更低。SKA2与肿瘤分期和免疫系统有关。此外,SKA2的188个共表达基因参与了一些过程,包括细胞周期、DNA复制等。肿瘤中的hsa-miR-19b-1-5p和hsa-miR-378a-5p表达较低,而这两种microRNA(miRNA)也与OS相关。SNHG14、SNHG15和SPCA6P-AS与hsa-378a-5p呈显著负相关,这三个长非编码RNA(lncRNA)与SKA2呈正相关(PSKA2是竞争性内源性RNA(ceRNA)的成员之一,与SPCA6P-AS和SKA2相关)。此外,它还与SPACA6P-AS/hsa-miR-378a-5p/SKA2、SNHG14/hsa-miR-378a-5p/SKA2和SNHG15/hsa-miR-378a-5p/SKA2有关,而这些RNA在肿瘤进展中发挥着重要作用:SKA2与HCC的OS、肿瘤分期和免疫浸润细胞有关。结论:SKA2 与 HCC 的 OS、肿瘤分期和免疫浸润细胞相关,因此,我们认为 SKA2 发挥着 ceRNA 的功能并影响着肿瘤的发生。这些发现为今后在 HCC 领域的研究奠定了基础。
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Oncogenic role of SKA2 and its ceRNA network in hepatocellular carcinoma based on a comprehensive analysis.

Background: Genetic alterations have important roles in cancer development and progression. SKA2 (spindle and kinetochore associated complex subunit 2) is a mitotic component that plays a critical role in maintaining the silence of the metaphase plate and spindle checkpoint. However, the exact role of SKA2 in hepatocellular carcinoma (HCC) remains unclear. The current study aimed to comprehensively identify the function of SKA2 in HCC.

Methods: We utilized various databases and bioinformatics tools, such as The Cancer Genome Atlas (TCGA), survminer package, Tumor Immune Estimation Resource (TIMER), cBioPortal website, clusterProfiler package, gene set enrichment analysis (GSEA), miRWalk, TargetScanHuman8.0, miRDB, DIANA and Cytoscape to identify the role of SKA2 in HCC.

Results: Our results showed that patients with HCC exhibited a high SKA2 expression. Further, the SKA2 high expression group had a worse overall survival (OS). And SKA2 was associated with tumor stage and the immune system. In addition, 188 co-expression genes of SKA2 participated in some processes including cell cycle, DNA replication and so on. The tumor had a lower hsa-miR-19b-1-5p and hsa-miR-378a-5p expression, and these two microRNAs (miRNAs) were also correlated with OS. SNHG14, SNHG15, and SPCA6P-AS were significantly negatively correlated with hsa-378a-5p, and these three long non-coding RNAs (lncRNAs) showed a positive correlation with SKA2 (P<0.05). SKA2 is a member of competing endogenous RNA (ceRNA). Moreover, it is related to SPACA6P-AS/hsa-miR-378a-5p/SKA2, SNHG14/hsa-miR-378a-5p/SKA2, and SNHG15/hsa-miR-378a-5p/SKA2, which play significant roles in tumor progression.

Conclusions: SKA2 is associated with OS, tumor stage, and immune infiltrating cells in HCC. Thus, we propose that SKA2 functions as a ceRNA and influences tumorigenesis. These findings lay the foundation for future research in the field of HCC.

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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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