<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Johnson NA</submitter><funding>Medical Research Council</funding><funding>NCI NIH HHS</funding><pagination>2273-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2745846</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>114(11)</volume><pubmed_abstract>BCL2 and MYC are oncogenes commonly deregulated in lymphomas. Concurrent BCL2 and MYC translocations (BCL2(+)/MYC(+)) were identified in 54 samples by karyotype and/or fluorescence in situ hybridization with the aim of correlating clinical and cytogenetic characteristics to overall survival. BCL2(+)/MYC(+) lymphomas were diagnosed as B-cell lymphoma unclassifiable (BCLU; n = 36) with features intermediate between Burkitt lymphoma and diffuse large B-cell lymphoma (DLBCL); DLBCL (n = 17), or follicular lymphoma (n = 1). Despite the presence of a t(14;18), 5 cases were BCL2 protein-negative. Nonimmunoglobulin gene/MYC (non-IG/MYC) translocations occurred in 24 of 54 cases (44%) and were highly associated with DLBCL morphology (P &lt; .001). Over a median follow-up of 5.3 years, 6 patients remai</pubmed_abstract><journal>Blood</journal><pubmed_title>Lymphomas with concurrent BCL2 and MYC translocations: the critical factors associated with survival.</pubmed_title><pmcid>PMC2745846</pmcid><funding_grant_id>MC_U132670597</funding_grant_id><funding_grant_id>UO1-CA84967-1</funding_grant_id><funding_grant_id>U01 CA084967</funding_grant_id><pubmed_authors>Ben-Neriah S</pubmed_authors><pubmed_authors>Siebert R</pubmed_authors><pubmed_authors>Connors JM</pubmed_authors><pubmed_authors>Savage KJ</pubmed_authors><pubmed_authors>Woods R</pubmed_authors><pubmed_authors>Klasa R</pubmed_authors><pubmed_authors>Ludkovski O</pubmed_authors><pubmed_authors>Kuruvilla J</pubmed_authors><pubmed_authors>Steidl C</pubmed_authors><pubmed_authors>Johnson NA</pubmed_authors><pubmed_authors>Gascoyne RD</pubmed_authors><pubmed_authors>Dyer MJ</pubmed_authors><pubmed_authors>Horsman DE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lymphomas with concurrent BCL2 and MYC translocations: the critical factors associated with survival.</name><description>BCL2 and MYC are oncogenes commonly deregulated in lymphomas. Concurrent BCL2 and MYC translocations (BCL2(+)/MYC(+)) were identified in 54 samples by karyotype and/or fluorescence in situ hybridization with the aim of correlating clinical and cytogenetic characteristics to overall survival. BCL2(+)/MYC(+) lymphomas were diagnosed as B-cell lymphoma unclassifiable (BCLU; n = 36) with features intermediate between Burkitt lymphoma and diffuse large B-cell lymphoma (DLBCL); DLBCL (n = 17), or follicular lymphoma (n = 1). Despite the presence of a t(14;18), 5 cases were BCL2 protein-negative. Nonimmunoglobulin gene/MYC (non-IG/MYC) translocations occurred in 24 of 54 cases (44%) and were highly associated with DLBCL morphology (P &lt; .001). Over a median follow-up of 5.3 years, 6 patients remai</description><dates><release>2009-01-01T00:00:00Z</release><publication>2009 Sep</publication><modification>2026-03-16T16:54:33.609Z</modification><creation>2025-09-01T03:06:37.554Z</creation></dates><accession>S-EPMC2745846</accession><cross_references><pubmed>19597184</pubmed><doi>10.1182/blood-2009-03-212191</doi></cross_references></HashMap>