<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>28(3)</volume><submitter>Huang P</submitter><pubmed_abstract>&lt;b>&lt;i>Background:&lt;/i>&lt;/b> Ferroptosis is associated with tumor development; however, its contribution to radioresistant head and neck cancer (HNC) remains unclear. In this study, we used bioinformatics analysis and &lt;i>in vitro&lt;/i> testing to explore ferroptosis-related genes associated with HNCs radiosensitivity. &lt;b>&lt;i>Materials and Methods:&lt;/i>&lt;/b> GSE9714, GSE90761, and The Cancer Genome Atlas (TCGA) datasets were searched to identify ferroptosis-related differentially expressed genes between radioresistant and radiosensitive HNCs or radiation-treated and nonradiation-treated HNCs. A protein-protein interaction analysis on identified hub genes was then performed. Receiver operating characteristic curves and Kaplan-Meier survival analysis were used to assess the diagnostic and prognostic potential of the hub genes. Cell counting kit-8, transwell assay, and flow cytometry were applied to examine the role of hub gene collagen type IV, alpha1 chain (&lt;i>COL4A1&lt;/i>) on the proliferation, migration, invasion, and apoptosis of TU686 cells. &lt;b>&lt;i>Results:&lt;/i>&lt;/b> Hub genes &lt;i>MMP10, MMP1, COL4A1, IFI27&lt;/i>, and &lt;i>INHBA&lt;/i> showed diagnostic potential for HNC and were negatively correlated with overall survival and disease-free survival in the TCGA dataset. Also, &lt;i>IL-1B, IFI27, INHBA,&lt;/i> and &lt;i>COL4A1&lt;/i> mRNA levels were significantly increased in TCGA patients with advanced clinical stages or receiving radiotherapy, whereas &lt;i>COL4A1, MMP10&lt;/i>, and &lt;i>INHBA&lt;/i> expressions were negatively correlated with immune infiltration. Furthermore, the knockdown of &lt;i>COL4A1&lt;/i> inhibited cell proliferation, migration, and invasion while promoting apoptosis in TU686 cells. &lt;b>&lt;i>Conclusion:&lt;/i>&lt;/b> Ferroptosis-related hub genes, such as &lt;i>COL4A1,&lt;/i> are potential diagnostic and prognostic indicators as well as therapeutic targets for HNC.</pubmed_abstract><journal>Genetic testing and molecular biomarkers</journal><pagination>100-113</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10979683</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Ferroptosis-Related Genes Are Associated with Radioresistance and Immune Suppression in Head and Neck Cancer.</pubmed_title><pmcid>PMC10979683</pmcid><pubmed_authors>Wang R</pubmed_authors><pubmed_authors>Ning X</pubmed_authors><pubmed_authors>Kang M</pubmed_authors><pubmed_authors>Huang P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ferroptosis-Related Genes Are Associated with Radioresistance and Immune Suppression in Head and Neck Cancer.</name><description>&lt;b>&lt;i>Background:&lt;/i>&lt;/b> Ferroptosis is associated with tumor development; however, its contribution to radioresistant head and neck cancer (HNC) remains unclear. In this study, we used bioinformatics analysis and &lt;i>in vitro&lt;/i> testing to explore ferroptosis-related genes associated with HNCs radiosensitivity. &lt;b>&lt;i>Materials and Methods:&lt;/i>&lt;/b> GSE9714, GSE90761, and The Cancer Genome Atlas (TCGA) datasets were searched to identify ferroptosis-related differentially expressed genes between radioresistant and radiosensitive HNCs or radiation-treated and nonradiation-treated HNCs. A protein-protein interaction analysis on identified hub genes was then performed. Receiver operating characteristic curves and Kaplan-Meier survival analysis were used to assess the diagnostic and prognostic potential of the hub genes. Cell counting kit-8, transwell assay, and flow cytometry were applied to examine the role of hub gene collagen type IV, alpha1 chain (&lt;i>COL4A1&lt;/i>) on the proliferation, migration, invasion, and apoptosis of TU686 cells. &lt;b>&lt;i>Results:&lt;/i>&lt;/b> Hub genes &lt;i>MMP10, MMP1, COL4A1, IFI27&lt;/i>, and &lt;i>INHBA&lt;/i> showed diagnostic potential for HNC and were negatively correlated with overall survival and disease-free survival in the TCGA dataset. Also, &lt;i>IL-1B, IFI27, INHBA,&lt;/i> and &lt;i>COL4A1&lt;/i> mRNA levels were significantly increased in TCGA patients with advanced clinical stages or receiving radiotherapy, whereas &lt;i>COL4A1, MMP10&lt;/i>, and &lt;i>INHBA&lt;/i> expressions were negatively correlated with immune infiltration. Furthermore, the knockdown of &lt;i>COL4A1&lt;/i> inhibited cell proliferation, migration, and invasion while promoting apoptosis in TU686 cells. &lt;b>&lt;i>Conclusion:&lt;/i>&lt;/b> Ferroptosis-related hub genes, such as &lt;i>COL4A1,&lt;/i> are potential diagnostic and prognostic indicators as well as therapeutic targets for HNC.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-01T21:47:23.759Z</modification><creation>2025-04-04T19:12:24.323Z</creation></dates><accession>S-EPMC10979683</accession><cross_references><pubmed>38478802</pubmed><doi>10.1089/gtmb.2023.0193</doi></cross_references></HashMap>