<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Dong Y</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> Immunotherapy with checkpoint inhibitors usually has a low response rate in some cutaneous melanoma (CM) cases due to its cold nature. Hence, identification of hot tumors is important to improve the immunotherapeutic efficacy and prognoses of CMs. &lt;b>Methods:&lt;/b> Fatty acid (FA) metabolism-related genes were extracted from the Gene Set Enrichment Analysis and used in the non-negative matrix factorization (NMF), copy number variation frequency, tumor mutation burden (TMB), and immune-related analyses, such as immunophenoscore (IPS). We generate a risk model and a nomogram for predicting patient prognoses and predicted the potential drugs for therapies using the Connectivity Map. Moreover, the NMF and the risk model were validated in a cohort of cases in the GSE65904 and G</pubmed_abstract><journal>Frontiers in genetics</journal><pagination>860067</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9527329</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Transcriptome profiles of fatty acid metabolism-related genes and immune infiltrates identify hot tumors for immunotherapy in cutaneous melanoma.</pubmed_title><pmcid>PMC9527329</pmcid><pubmed_authors>Dong Y</pubmed_authors><pubmed_authors>Simayi M</pubmed_authors><pubmed_authors>Tang B</pubmed_authors><pubmed_authors>Lv D</pubmed_authors><pubmed_authors>Chen C</pubmed_authors><pubmed_authors>Zhao Z</pubmed_authors><pubmed_authors>Xu Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcriptome profiles of fatty acid metabolism-related genes and immune infiltrates identify hot tumors for immunotherapy in cutaneous melanoma.</name><description>&lt;b>Background:&lt;/b> Immunotherapy with checkpoint inhibitors usually has a low response rate in some cutaneous melanoma (CM) cases due to its cold nature. Hence, identification of hot tumors is important to improve the immunotherapeutic efficacy and prognoses of CMs. &lt;b>Methods:&lt;/b> Fatty acid (FA) metabolism-related genes were extracted from the Gene Set Enrichment Analysis and used in the non-negative matrix factorization (NMF), copy number variation frequency, tumor mutation burden (TMB), and immune-related analyses, such as immunophenoscore (IPS). We generate a risk model and a nomogram for predicting patient prognoses and predicted the potential drugs for therapies using the Connectivity Map. Moreover, the NMF and the risk model were validated in a cohort of cases in the GSE65904 and G</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-19T10:01:47.487Z</modification><creation>2025-04-19T10:01:47.487Z</creation></dates><accession>S-EPMC9527329</accession><cross_references><pubmed>36199579</pubmed><doi>10.3389/fgene.2022.860067</doi></cross_references></HashMap>