<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sahasrabuddhe AA</submitter><funding>National Institutes of Health (NIH)</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIGMS NIH HHS</funding><pagination>838-861</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11962402</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(4)</volume><pubmed_abstract>&lt;h4>Significance&lt;/h4>We describe the identification of a previously unrecognized ubiquitin ligase-substrate (FBXO45-GEF-H1) regulatory axis that plays an important role in germinal center formation and pathogenesis of common BCLs. These studies reveal novel insights linking dysregulated ubiquitin-mediated control to exploitable vulnerabilities and novel therapeutic strategies for these cancers.</pubmed_abstract><journal>Cancer discovery</journal><pubmed_title>The FBXO45-GEF-H1 Axis Controls Germinal Center Formation and B-cell Lymphomagenesis.</pubmed_title><pmcid>PMC11962402</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>R01 CA231021</funding_grant_id><funding_grant_id>R35 GM136250</funding_grant_id><funding_grant_id>R01CA231021</funding_grant_id><funding_grant_id>R01 HL123899</funding_grant_id><pubmed_authors>Pillai V</pubmed_authors><pubmed_authors>Siebert R</pubmed_authors><pubmed_authors>Rottapel R</pubmed_authors><pubmed_authors>Hogaboam CM</pubmed_authors><pubmed_authors>Sahasrabuddhe AA</pubmed_authors><pubmed_authors>Kim J</pubmed_authors><pubmed_authors>Raabe TD</pubmed_authors><pubmed_authors>Morin RD</pubmed_authors><pubmed_authors>McFetridge C</pubmed_authors><pubmed_authors>Schlesner M</pubmed_authors><pubmed_authors>Onder O</pubmed_authors><pubmed_authors>Bailey NG</pubmed_authors><pubmed_authors>Liang HC</pubmed_authors><pubmed_authors>Basrur V</pubmed_authors><pubmed_authors>Lopez C</pubmed_authors><pubmed_authors>Wu R</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Li MM</pubmed_authors><pubmed_authors>Moro L</pubmed_authors><pubmed_authors>Szankasi P</pubmed_authors><pubmed_authors>Elenitoba-Johnson KSJ</pubmed_authors><pubmed_authors>Chhipa RR</pubmed_authors><pubmed_authors>Kapoor R</pubmed_authors><pubmed_authors>Dreval K</pubmed_authors><pubmed_authors>Morrissette JJD</pubmed_authors><pubmed_authors>Staudt LM</pubmed_authors><pubmed_authors>Conlon KP</pubmed_authors><pubmed_authors>Pagano M</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Ma K</pubmed_authors><pubmed_authors>Lim MS</pubmed_authors><pubmed_authors>Van Arnam JS</pubmed_authors></additional><is_claimable>false</is_claimable><name>The FBXO45-GEF-H1 Axis Controls Germinal Center Formation and B-cell Lymphomagenesis.</name><description>&lt;h4>Significance&lt;/h4>We describe the identification of a previously unrecognized ubiquitin ligase-substrate (FBXO45-GEF-H1) regulatory axis that plays an important role in germinal center formation and pathogenesis of common BCLs. These studies reveal novel insights linking dysregulated ubiquitin-mediated control to exploitable vulnerabilities and novel therapeutic strategies for these cancers.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2026-04-08T19:51:25.352Z</modification><creation>2026-04-08T14:30:07.747Z</creation></dates><accession>S-EPMC11962402</accession><cross_references><pubmed>39820335</pubmed><doi>10.1158/2159-8290.CD-24-0442</doi></cross_references></HashMap>