<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>84(5)</volume><submitter>Tatman PD</submitter><pubmed_abstract>&lt;b>Background&lt;/b>  Epigenetics may predict treatment sensitivity and clinical course for patients with meningiomas more accurately than histopathology. Nonetheless, targeting epigenetic mechanisms is understudied for pharmacotherapeutic development for these tumors. The bio-molecular insights and potential therapeutic development of meningioma epigenetics led us to investigate epigenetic inhibition in meningiomas. &lt;b>Methods&lt;/b>  We screened a 43-tumor cohort using a 139-compound epigenetic inhibitor library to assess sensitivity of relevant meningioma subgroups to epigenetic inhibition. The cohort was composed of 5 cell lines and 38 tumors cultured directly from surgery; mean patient age was 56.6 years ± 13.9 standard deviation. Tumor categories: 38 primary tumors, 5 recurrent; 33 from fe</pubmed_abstract><journal>Journal of neurological surgery. Part B, Skull base</journal><pagination>452-462</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10477014</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>High-Throughput Screening of Epigenetic Inhibitors in Meningiomas Identifies HDAC, G9a, and Jumonji-Domain Inhibition as Potential Therapies.</pubmed_title><pmcid>PMC10477014</pmcid><pubmed_authors>Graner MW</pubmed_authors><pubmed_authors>Ormond DR</pubmed_authors><pubmed_authors>Tatman PD</pubmed_authors><pubmed_authors>Youssef AS</pubmed_authors><pubmed_authors>Wroblewski TH</pubmed_authors><pubmed_authors>Jensen RL</pubmed_authors><pubmed_authors>Fringuello AR</pubmed_authors><pubmed_authors>Foreman WB</pubmed_authors><pubmed_authors>Damek DM</pubmed_authors><pubmed_authors>Scherer SR</pubmed_authors><pubmed_authors>Lillehei KO</pubmed_authors></additional><is_claimable>false</is_claimable><name>High-Throughput Screening of Epigenetic Inhibitors in Meningiomas Identifies HDAC, G9a, and Jumonji-Domain Inhibition as Potential Therapies.</name><description>&lt;b>Background&lt;/b>  Epigenetics may predict treatment sensitivity and clinical course for patients with meningiomas more accurately than histopathology. Nonetheless, targeting epigenetic mechanisms is understudied for pharmacotherapeutic development for these tumors. The bio-molecular insights and potential therapeutic development of meningioma epigenetics led us to investigate epigenetic inhibition in meningiomas. &lt;b>Methods&lt;/b>  We screened a 43-tumor cohort using a 139-compound epigenetic inhibitor library to assess sensitivity of relevant meningioma subgroups to epigenetic inhibition. The cohort was composed of 5 cell lines and 38 tumors cultured directly from surgery; mean patient age was 56.6 years ± 13.9 standard deviation. Tumor categories: 38 primary tumors, 5 recurrent; 33 from fe</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Oct</publication><modification>2025-04-05T12:36:16.545Z</modification><creation>2025-04-05T12:36:16.545Z</creation></dates><accession>S-EPMC10477014</accession><cross_references><pubmed>37671294</pubmed><doi>10.1055/a-1885-1257</doi></cross_references></HashMap>