S B Shanmugam, J Vijayashree Priyadharsini, P Anitha, A S Smiline Girija, A Paramasivam
{"title":"Dysregulated genes in HIGK-treated <i>F. nucleatum </i>and their possible association with HNSCC.","authors":"S B Shanmugam, J Vijayashree Priyadharsini, P Anitha, A S Smiline Girija, A Paramasivam","doi":"10.22099/mbrc.2024.50171.1982","DOIUrl":null,"url":null,"abstract":"<p><p>The present study aims to identify the differentially expressed genes in HIGK treated with <i>Fusobacterium nucleatum (Fn)</i> and their possible role in establishing head and neck squamous cell carcinoma. The study design follows a computational approach wherein multiple databases and tools are used to derive the possible association between <i>Fn</i> exposure and the development of HNSCC. The GEOmnibus dataset GSE6927 provided data on the differentially expressed genes in the HIGK treated with <i>Fn</i>. The GEO2R analysis revealed 22 differentially expressed genes in HIGK cells treated with <i>Fn</i>. The expression profile of these genes was then analyzed in the HNSCC (TCGA, Firehose Legacy) dataset employing the UALCAN database. The present study revealed 5 genes <i>viz.,</i> <i>GSDMD</i>, <i>NUP214</i>, <i>ZNF426</i>, <i>FUT2</i>, and <i>SERPINB2</i> exhibiting similar expression patterns in <i>Fn</i>-treated HIGK and HNSCC datasets. The <i>GSDMD</i> and <i>NUP214</i> were found to be upregulated, and the genes <i>ZNF426</i>, <i>FUT2</i>, and <i>SERPINB2</i> were downregulated. Among the five genes, the <i>ZNF426</i> demonstrated a significant association with the survival of HNSCC patients. The low expression of <i>ZNF426</i> presented a poor prognosis compared to the high expression. The study's results identified <i>ZNF426</i> as a candidate gene involved in <i>Fusobacterium nucleatum</i> infection and HNSCC. Validating this result is necessary to gain insights into the role of the <i>ZNF426</i> gene in developing HNSCC. Furthermore, probing the epigenetic factors targeting <i>ZNF426</i> can be a potential therapeutic lead.</p>","PeriodicalId":19025,"journal":{"name":"Molecular Biology Research Communications","volume":"14 1","pages":"59-71"},"PeriodicalIF":1.5000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11624608/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Biology Research Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22099/mbrc.2024.50171.1982","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The present study aims to identify the differentially expressed genes in HIGK treated with Fusobacterium nucleatum (Fn) and their possible role in establishing head and neck squamous cell carcinoma. The study design follows a computational approach wherein multiple databases and tools are used to derive the possible association between Fn exposure and the development of HNSCC. The GEOmnibus dataset GSE6927 provided data on the differentially expressed genes in the HIGK treated with Fn. The GEO2R analysis revealed 22 differentially expressed genes in HIGK cells treated with Fn. The expression profile of these genes was then analyzed in the HNSCC (TCGA, Firehose Legacy) dataset employing the UALCAN database. The present study revealed 5 genes viz.,GSDMD, NUP214, ZNF426, FUT2, and SERPINB2 exhibiting similar expression patterns in Fn-treated HIGK and HNSCC datasets. The GSDMD and NUP214 were found to be upregulated, and the genes ZNF426, FUT2, and SERPINB2 were downregulated. Among the five genes, the ZNF426 demonstrated a significant association with the survival of HNSCC patients. The low expression of ZNF426 presented a poor prognosis compared to the high expression. The study's results identified ZNF426 as a candidate gene involved in Fusobacterium nucleatum infection and HNSCC. Validating this result is necessary to gain insights into the role of the ZNF426 gene in developing HNSCC. Furthermore, probing the epigenetic factors targeting ZNF426 can be a potential therapeutic lead.
期刊介绍:
“Molecular Biology Research Communications” (MBRC) is an international journal of Molecular Biology. It is published quarterly by Shiraz University (Iran). The MBRC is a fully peer-reviewed journal. The journal welcomes submission of Original articles, Short communications, Invited review articles, and Letters to the Editor which meets the general criteria of significance and scientific excellence in all fields of “Molecular Biology”.