<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Baluszek S</submitter><funding>National Science Centre, Poland</funding><pagination>3324</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12564510</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(20)</volume><pubmed_abstract>&lt;b>Background&lt;/b>: Meningiomas are common intracranial tumors in adults. Most are benign WHO grade I (GI) tumors, while approximately 20% are diagnosed as more aggressive WHO grade II (GII) and grade III (GIII) meningiomas. The study aimed to identify genes with tumor grade-related expression and to assess their functional relevance. &lt;b>Methods&lt;/b>: RNA sequencing (RNA-seq) was performed to analyze transcriptomes of benign meningothelial (&lt;i>n&lt;/i> = 19) and fibrous (&lt;i>n&lt;/i> = 11), atypical (&lt;i>n&lt;/i> = 18) and anaplastic (&lt;i>n&lt;/i> = 12) meningiomas. The data were analyzed for differential genes expression and Gene Set Enrichment Analysis (GSEA). A deposited scRNA-seq dataset was used to define meningioma cellular composition and cell type-specific gene expression enabling deconvolution of </pubmed_abstract><journal>Cancers</journal><pubmed_title>Determining the Biological Features of Aggressive Meningioma Growth with Transcriptomic Profiling.</pubmed_title><pmcid>PMC12564510</pmcid><funding_grant_id>2018/29/B/NZ5/02035</funding_grant_id><pubmed_authors>Baluszek S</pubmed_authors><pubmed_authors>Ozieblo A</pubmed_authors><pubmed_authors>Bujko M</pubmed_authors><pubmed_authors>Mysliwy I</pubmed_authors><pubmed_authors>Kober P</pubmed_authors><pubmed_authors>Mandat T</pubmed_authors><pubmed_authors>Jezewski MP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Determining the Biological Features of Aggressive Meningioma Growth with Transcriptomic Profiling.</name><description>&lt;b>Background&lt;/b>: Meningiomas are common intracranial tumors in adults. Most are benign WHO grade I (GI) tumors, while approximately 20% are diagnosed as more aggressive WHO grade II (GII) and grade III (GIII) meningiomas. The study aimed to identify genes with tumor grade-related expression and to assess their functional relevance. &lt;b>Methods&lt;/b>: RNA sequencing (RNA-seq) was performed to analyze transcriptomes of benign meningothelial (&lt;i>n&lt;/i> = 19) and fibrous (&lt;i>n&lt;/i> = 11), atypical (&lt;i>n&lt;/i> = 18) and anaplastic (&lt;i>n&lt;/i> = 12) meningiomas. The data were analyzed for differential genes expression and Gene Set Enrichment Analysis (GSEA). A deposited scRNA-seq dataset was used to define meningioma cellular composition and cell type-specific gene expression enabling deconvolution of </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-07-02T03:11:14.811Z</modification><creation>2026-07-02T03:08:48.947Z</creation></dates><accession>S-EPMC12564510</accession><cross_references><pubmed>41154381</pubmed><doi>10.3390/cancers17203324</doi></cross_references></HashMap>