<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lu J</submitter><funding>Basic and Applied Basic Research Foundation of Guangdong Province</funding><funding>the Scientific and Technological Planning Project of Guangzhou City</funding><pagination>37</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11853526</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>m6A methylation modification is a new regulatory mechanism involved in tumorigenesis and tumor-immunity interaction. However, its impact on glioma immune microenvironment and clinical outcomes remains unclear.&lt;h4>Methods&lt;/h4>Comprehensive expression profiles of 18 m6A regulators were used to identify molecular subtypes exhibiting distinct m6A modification patterns in 1673 glioma samples sourced from public datasets. A multi-genes signature was constructed for predicting clinical outcomes and response to immunotherapy in glioma patients. Immunohistochemistry and cellular experiments were performed for validation.&lt;h4>Results&lt;/h4>Two m6A subtypes of gliomas were identified. The m6A-low-risk subtype was characterized by paucity of immune infiltrates; While the m6A-high-risk </pubmed_abstract><journal>BMC medical genomics</journal><pubmed_title>m6A regulator-based molecular classification and hub genes associated with immune infiltration characteristics and clinical outcomes in diffuse gliomas.</pubmed_title><pmcid>PMC11853526</pmcid><funding_grant_id>202201010515</funding_grant_id><funding_grant_id>2022A1515111118</funding_grant_id><funding_grant_id>2023A04J1782</funding_grant_id><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Hu W</pubmed_authors><pubmed_authors>Lu J</pubmed_authors><pubmed_authors>Sai K</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Jiang P</pubmed_authors></additional><is_claimable>false</is_claimable><name>m6A regulator-based molecular classification and hub genes associated with immune infiltration characteristics and clinical outcomes in diffuse gliomas.</name><description>&lt;h4>Background&lt;/h4>m6A methylation modification is a new regulatory mechanism involved in tumorigenesis and tumor-immunity interaction. However, its impact on glioma immune microenvironment and clinical outcomes remains unclear.&lt;h4>Methods&lt;/h4>Comprehensive expression profiles of 18 m6A regulators were used to identify molecular subtypes exhibiting distinct m6A modification patterns in 1673 glioma samples sourced from public datasets. A multi-genes signature was constructed for predicting clinical outcomes and response to immunotherapy in glioma patients. Immunohistochemistry and cellular experiments were performed for validation.&lt;h4>Results&lt;/h4>Two m6A subtypes of gliomas were identified. The m6A-low-risk subtype was characterized by paucity of immune infiltrates; While the m6A-high-risk </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2025-04-03T23:44:21.99Z</modification><creation>2025-04-03T23:44:21.99Z</creation></dates><accession>S-EPMC11853526</accession><cross_references><pubmed>39994800</pubmed><doi>10.1186/s12920-025-02104-9</doi></cross_references></HashMap>