{"title":"Construction and clinical evaluation of N6-methyladenosine risk signature of YTHDC2, IGF2BP2, and HNRNPC in head and neck squamous cell carcinoma.","authors":"Qiangwei Yue, Le Xu, Dongsheng Zhang","doi":"10.7518/hxkq.2022.06.012","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>This work aimed to construct N6-methyladenosine (m<sup>6</sup>A) regulator-based prognostic signature and evaluate the prognostic value and the intervention on tumor immune microenvironment of this m<sup>6</sup>A risk signature.</p><p><strong>Methods: </strong>Using transcriptome and clinical data of head and neck squamous cell carcinoma (HNSCC) from The Cancer Genome Atlas (TCGA), we profiled m<sup>6</sup>A regulators and constructed an m<sup>6</sup>A risk signature. The relationship between m<sup>6</sup>A modulation and immune function was studied by differential gene expression, cell type enrichment, and correlation analyses.</p><p><strong>Results: </strong>Fifteen m<sup>6</sup>A regulators had aberrant expression in HNSCC. A three-gene m<sup>6</sup>A prognostic signature (i.e., YTHDC2, IGF2BP2, and HNRNPC) was constructed and identified as an independent prognostic indicator for HNSCC. The m<sup>6</sup>A regulator signature-based high-risk group revealed pro-tumoral immune microenvironment due to the dysregulation of immune-related gene expression, abnormal enrichment of multiple immunocytes, and production of immunoregulatory factors.</p><p><strong>Conclusions: </strong>This comprehensive analysis of m<sup>6</sup>A regulators and tumor immune landscape in HNSCC revealed that the m<sup>6</sup>A signature of YTHDC2, IGF2BP2, and HNRNPC could serve as a promising biomarker for monitoring HNSCC development and may be a potential target for tumor therapy in the future.</p>","PeriodicalId":35800,"journal":{"name":"华西口腔医学杂志","volume":"40 6","pages":"704-709"},"PeriodicalIF":0.0000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763947/pdf/wcjs-40-06-704.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"华西口腔医学杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.7518/hxkq.2022.06.012","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives: This work aimed to construct N6-methyladenosine (m6A) regulator-based prognostic signature and evaluate the prognostic value and the intervention on tumor immune microenvironment of this m6A risk signature.
Methods: Using transcriptome and clinical data of head and neck squamous cell carcinoma (HNSCC) from The Cancer Genome Atlas (TCGA), we profiled m6A regulators and constructed an m6A risk signature. The relationship between m6A modulation and immune function was studied by differential gene expression, cell type enrichment, and correlation analyses.
Results: Fifteen m6A regulators had aberrant expression in HNSCC. A three-gene m6A prognostic signature (i.e., YTHDC2, IGF2BP2, and HNRNPC) was constructed and identified as an independent prognostic indicator for HNSCC. The m6A regulator signature-based high-risk group revealed pro-tumoral immune microenvironment due to the dysregulation of immune-related gene expression, abnormal enrichment of multiple immunocytes, and production of immunoregulatory factors.
Conclusions: This comprehensive analysis of m6A regulators and tumor immune landscape in HNSCC revealed that the m6A signature of YTHDC2, IGF2BP2, and HNRNPC could serve as a promising biomarker for monitoring HNSCC development and may be a potential target for tumor therapy in the future.
期刊介绍:
West China Journal of Stomatology (WCJS, pISSN 1000-1182, eISSN 2618-0456, CN 51-1169/R), published bimonthly, is a peer-reviewed Open Access journal, hosted by Sichuan university and Ministry of Education of the People's Republic of China. WCJS was established in 1983 and indexed in Medline/Pubmed, SCOPUS, EBSCO, Chemical Abstract(CA), CNKI, WANFANG Data, etc.