{"title":"基于综合分析的 SKA2 及其 ceRNA 网络在肝细胞癌中的致癌作用","authors":"Wanxue Hu, Xiaoyi Hu, Yongchao Zhu, Min Li, Hongyu Meng, Hongbo Zhao","doi":"10.21037/tcr-24-833","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Genetic alterations have important roles in cancer development and progression. <i>SKA2</i> (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 <i>SKA2</i> in hepatocellular carcinoma (HCC) remains unclear. The current study aimed to comprehensively identify the function of <i>SKA2</i> in HCC.</p><p><strong>Methods: </strong>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 <i>SKA2</i> in HCC.</p><p><strong>Results: </strong>Our results showed that patients with HCC exhibited a high <i>SKA2</i> expression. Further, the <i>SKA2</i> high expression group had a worse overall survival (OS). And <i>SKA2</i> was associated with tumor stage and the immune system. In addition, 188 co-expression genes of <i>SKA2</i> 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 <i>SKA2</i> (P<0.05). <i>SKA2</i> is a member of competing endogenous RNA (ceRNA). Moreover, it is related to SPACA6P-AS/hsa-miR-378a-5p/<i>SKA2</i>, SNHG14/hsa-miR-378a-5p/<i>SKA2</i>, and SNHG15/hsa-miR-378a-5p/<i>SKA2</i>, which play significant roles in tumor progression.</p><p><strong>Conclusions: </strong><i>SKA2</i> is associated with OS, tumor stage, and immune infiltrating cells in HCC. Thus, we propose that <i>SKA2</i> functions as a ceRNA and influences tumorigenesis. These findings lay the foundation for future research in the field of HCC.</p>","PeriodicalId":23216,"journal":{"name":"Translational cancer research","volume":"13 10","pages":"5190-5201"},"PeriodicalIF":1.5000,"publicationDate":"2024-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11543042/pdf/","citationCount":"0","resultStr":"{\"title\":\"Oncogenic role of <i>SKA2</i> and its ceRNA network in hepatocellular carcinoma based on a comprehensive analysis.\",\"authors\":\"Wanxue Hu, Xiaoyi Hu, Yongchao Zhu, Min Li, Hongyu Meng, Hongbo Zhao\",\"doi\":\"10.21037/tcr-24-833\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Genetic alterations have important roles in cancer development and progression. <i>SKA2</i> (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 <i>SKA2</i> in hepatocellular carcinoma (HCC) remains unclear. The current study aimed to comprehensively identify the function of <i>SKA2</i> in HCC.</p><p><strong>Methods: </strong>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 <i>SKA2</i> in HCC.</p><p><strong>Results: </strong>Our results showed that patients with HCC exhibited a high <i>SKA2</i> expression. Further, the <i>SKA2</i> high expression group had a worse overall survival (OS). And <i>SKA2</i> was associated with tumor stage and the immune system. In addition, 188 co-expression genes of <i>SKA2</i> 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 <i>SKA2</i> (P<0.05). <i>SKA2</i> is a member of competing endogenous RNA (ceRNA). Moreover, it is related to SPACA6P-AS/hsa-miR-378a-5p/<i>SKA2</i>, SNHG14/hsa-miR-378a-5p/<i>SKA2</i>, and SNHG15/hsa-miR-378a-5p/<i>SKA2</i>, which play significant roles in tumor progression.</p><p><strong>Conclusions: </strong><i>SKA2</i> is associated with OS, tumor stage, and immune infiltrating cells in HCC. Thus, we propose that <i>SKA2</i> functions as a ceRNA and influences tumorigenesis. These findings lay the foundation for future research in the field of HCC.</p>\",\"PeriodicalId\":23216,\"journal\":{\"name\":\"Translational cancer research\",\"volume\":\"13 10\",\"pages\":\"5190-5201\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2024-10-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11543042/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Translational cancer research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.21037/tcr-24-833\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/10/29 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational cancer research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.21037/tcr-24-833","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/10/29 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
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.
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.