SKA1/2/3 link to poor prognosis and immune infiltration of head and neck squamous cell carcinomas.

IF 1.5 4区 医学 Q4 ONCOLOGY
Translational cancer research Pub Date : 2024-11-30 Epub Date: 2024-11-08 DOI:10.21037/tcr-24-862
Churen Zhang, Jianguo Ke, Jia Li, Qiaoling Cai
{"title":"<i>SKA1/2/3</i> link to poor prognosis and immune infiltration of head and neck squamous cell carcinomas.","authors":"Churen Zhang, Jianguo Ke, Jia Li, Qiaoling Cai","doi":"10.21037/tcr-24-862","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Head and neck squamous cell carcinomas (HNSCs) are a diverse collection of tumors that originate in the oral cavity, pharynx, and larynx and pose a severe threat to human health, contributing to a fast-rising burden of cancer morbidity and mortality. The search for prognostic biomarkers of HNSC has been a hot topic. Spindle and kinetochore-associated (<i>SKA</i>) complex, including three members <i>SKA1/2/3</i>, which stabilize the spindle microtubules at the kinetosite during mitosis metaphase, has been demonstrated to be associated with poor prognosis of different cancers. The function of <i>SKA1/2/3</i> in HNSC remains to be investigated. We used a vast variety of public datasets and web-based technologies to investigate <i>SKA</i> complex expression and its link to patient prognosis, and discovered multiple pathways by which the <i>SKA</i> complex is regulated in HNSC.</p><p><strong>Methods: </strong>The Cancer Genome Atlas (TCGA) database was used to determine <i>SKA1/2/3</i> expression level in HNSC. <i>SKA1/2/3</i>-related proteins level and immune cells infiltration level were identified. Metascape was used for Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis. GSE31056 from Gene Expression Omnibus (GEO) database was used as an external dataset for data validation. A nomogram containing <i>SKA1/2/3</i> for the prognosis of HNSC patients was established.</p><p><strong>Results: </strong><i>SKA1/2/3</i> were highly expressed in HNSC. High expression of <i>SKA2</i> was significantly related to the poor overall survival (OS) and poor disease-free survival (DFS) of HNSC patients. <i>SKA1/2/3</i> and the related proteins were enriched in cell division, chromosome segregation, and mitotic cell cycle. <i>SKA1/2/3</i> expression was obviously positively correlated to several immune cells' infiltration. The expression values of <i>SKA1/2/3</i> were higher in tumors than in healthy tissues in GSE31056.</p><p><strong>Conclusions: </strong><i>SKA1/2/3</i> were shown to be related to the prognosis and immune cell infiltration of HNSC, which could be used as biological markers and therapeutic targets for HNSC.</p>","PeriodicalId":23216,"journal":{"name":"Translational cancer research","volume":"13 11","pages":"6057-6069"},"PeriodicalIF":1.5000,"publicationDate":"2024-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11651734/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational cancer research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.21037/tcr-24-862","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/8 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Head and neck squamous cell carcinomas (HNSCs) are a diverse collection of tumors that originate in the oral cavity, pharynx, and larynx and pose a severe threat to human health, contributing to a fast-rising burden of cancer morbidity and mortality. The search for prognostic biomarkers of HNSC has been a hot topic. Spindle and kinetochore-associated (SKA) complex, including three members SKA1/2/3, which stabilize the spindle microtubules at the kinetosite during mitosis metaphase, has been demonstrated to be associated with poor prognosis of different cancers. The function of SKA1/2/3 in HNSC remains to be investigated. We used a vast variety of public datasets and web-based technologies to investigate SKA complex expression and its link to patient prognosis, and discovered multiple pathways by which the SKA complex is regulated in HNSC.

Methods: The Cancer Genome Atlas (TCGA) database was used to determine SKA1/2/3 expression level in HNSC. SKA1/2/3-related proteins level and immune cells infiltration level were identified. Metascape was used for Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis. GSE31056 from Gene Expression Omnibus (GEO) database was used as an external dataset for data validation. A nomogram containing SKA1/2/3 for the prognosis of HNSC patients was established.

Results: SKA1/2/3 were highly expressed in HNSC. High expression of SKA2 was significantly related to the poor overall survival (OS) and poor disease-free survival (DFS) of HNSC patients. SKA1/2/3 and the related proteins were enriched in cell division, chromosome segregation, and mitotic cell cycle. SKA1/2/3 expression was obviously positively correlated to several immune cells' infiltration. The expression values of SKA1/2/3 were higher in tumors than in healthy tissues in GSE31056.

Conclusions: SKA1/2/3 were shown to be related to the prognosis and immune cell infiltration of HNSC, which could be used as biological markers and therapeutic targets for HNSC.

SKA1/2/3与头颈部鳞状细胞癌预后不良及免疫浸润有关。
背景:头颈部鳞状细胞癌(HNSCs)是一种起源于口腔、咽部和喉部的多种肿瘤,对人类健康构成严重威胁,导致癌症发病率和死亡率迅速上升。寻找HNSC的预后生物标志物一直是一个热门话题。纺锤体和着丝点相关复合物(SKA)包括三个成员SKA1/2/3,在有丝分裂中期稳定着丝点处的纺锤体微管,已被证明与不同癌症的不良预后有关。SKA1/2/3在HNSC中的功能有待进一步研究。我们使用了大量的公共数据集和基于网络的技术来研究SKA复合物的表达及其与患者预后的联系,并发现了SKA复合物在HNSC中受到调节的多种途径。方法:采用肿瘤基因组图谱(Cancer Genome Atlas, TCGA)数据库检测SKA1/2/3在HNSC中的表达水平。检测ska1 /2/3相关蛋白水平及免疫细胞浸润水平。Metascape用于基因本体(GO)和京都基因与基因组百科全书(KEGG)途径分析。使用GEO数据库中的GSE31056作为外部数据集进行数据验证。建立含SKA1/2/3的HNSC患者预后图。结果:SKA1/2/3在HNSC中高表达。SKA2的高表达与HNSC患者的总生存期(OS)和无病生存期(DFS)差显著相关。SKA1/2/3及相关蛋白在细胞分裂、染色体分离和有丝分裂细胞周期中富集。SKA1/2/3的表达与多种免疫细胞浸润呈显著正相关。SKA1/2/3在GSE31056肿瘤组织中的表达量高于健康组织。结论:SKA1/2/3与HNSC的预后及免疫细胞浸润有关,可作为HNSC的生物学标志物和治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信