<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(12)</volume><submitter>Schmidt M</submitter><pubmed_abstract>Meningiomas are frequent central nervous system tumors. Although most meningiomas are benign (WHO grade I) and curable by surgery, WHO grade II and III tumors remain therapeutically challenging due to frequent recurrence. Interestingly, relapse also occurs in some WHO grade I meningiomas. Hence, we investigated the transcriptional features defining aggressive (recurrent, malignantly progressing or WHO grade III) meningiomas in 144 cases. Meningiomas were categorized into non-recurrent (NR), recurrent (R), and tumors undergoing malignant progression (M) in addition to their WHO grade. Unsupervised transcriptomic analysis in 62 meningiomas revealed transcriptional profiles lining up according to WHO grade and clinical subgroup. Notably aggressive subgroups (R+M tumors and WHO grade III) shar</pubmed_abstract><journal>Oncotarget</journal><pagination>14551-68</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4924735</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Transcriptomic analysis of aggressive meningiomas identifies PTTG1 and LEPR as prognostic biomarkers independent of WHO grade.</pubmed_title><pmcid>PMC4924735</pmcid><pubmed_authors>Kessler AF</pubmed_authors><pubmed_authors>Grabe N</pubmed_authors><pubmed_authors>Simon M</pubmed_authors><pubmed_authors>Ketter R</pubmed_authors><pubmed_authors>Rapp C</pubmed_authors><pubmed_authors>Urbschat S</pubmed_authors><pubmed_authors>Senft C</pubmed_authors><pubmed_authors>Schmidt M</pubmed_authors><pubmed_authors>Schefzyk S</pubmed_authors><pubmed_authors>Lahrmann B</pubmed_authors><pubmed_authors>Jungk C</pubmed_authors><pubmed_authors>Mock A</pubmed_authors><pubmed_authors>von Deimling A</pubmed_authors><pubmed_authors>Herold-Mende C</pubmed_authors><pubmed_authors>Warta R</pubmed_authors><pubmed_authors>Lohr M</pubmed_authors><pubmed_authors>Gousias K</pubmed_authors><pubmed_authors>Westphal M</pubmed_authors><pubmed_authors>Ull AT</pubmed_authors><pubmed_authors>Sahm F</pubmed_authors><pubmed_authors>Roesch S</pubmed_authors><pubmed_authors>Beckhove P</pubmed_authors><pubmed_authors>Reuss D</pubmed_authors><pubmed_authors>Lamszus K</pubmed_authors><pubmed_authors>Unterberg A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcriptomic analysis of aggressive meningiomas identifies PTTG1 and LEPR as prognostic biomarkers independent of WHO grade.</name><description>Meningiomas are frequent central nervous system tumors. Although most meningiomas are benign (WHO grade I) and curable by surgery, WHO grade II and III tumors remain therapeutically challenging due to frequent recurrence. Interestingly, relapse also occurs in some WHO grade I meningiomas. Hence, we investigated the transcriptional features defining aggressive (recurrent, malignantly progressing or WHO grade III) meningiomas in 144 cases. Meningiomas were categorized into non-recurrent (NR), recurrent (R), and tumors undergoing malignant progression (M) in addition to their WHO grade. Unsupervised transcriptomic analysis in 62 meningiomas revealed transcriptional profiles lining up according to WHO grade and clinical subgroup. Notably aggressive subgroups (R+M tumors and WHO grade III) shar</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Mar</publication><modification>2026-05-30T04:22:08.817Z</modification><creation>2019-03-27T02:17:07Z</creation></dates><accession>S-EPMC4924735</accession><cross_references><pubmed>26894859</pubmed><doi>10.18632/oncotarget.7396</doi></cross_references></HashMap>