<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hoppe MM</submitter><funding>Cancer Research UK</funding><funding>Singapore Ministry of Education</funding><funding>NIHR Cambridge Biomedical Research Centre</funding><funding>Medical Research Council</funding><funding>CRUK and EPSRC Cancer Imaging Centre in Cambridge and Manchester</funding><funding>National Research Foundation Singapore</funding><funding>National Medical Research Council</funding><funding>Wellcome Trust</funding><funding>Italian Foundation for Cancer Research</funding><pagination>1144-1163</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10157367</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(5)</volume><pubmed_abstract>Cancers often overexpress multiple clinically relevant oncogenes, but it is not known if combinations of oncogenes in cellular subpopulations within a cancer influence clinical outcomes. Using quantitative multispectral imaging of the prognostically relevant oncogenes MYC, BCL2, and BCL6 in diffuse large B-cell lymphoma (DLBCL), we show that the percentage of cells with a unique combination MYC+BCL2+BCL6- (M+2+6-) consistently predicts survival across four independent cohorts (n = 449), an effect not observed with other combinations including M+2+6+. We show that the M+2+6- percentage can be mathematically derived from quantitative measurements of the individual oncogenes and correlates with survival in IHC (n = 316) and gene expression (n = 2,521) datasets. Comparative bulk/single-cell tr</pubmed_abstract><journal>Cancer discovery</journal><pubmed_title>Patterns of Oncogene Coexpression at Single-Cell Resolution Influence Survival in Lymphoma.</pubmed_title><pmcid>PMC10157367</pmcid><funding_grant_id>100072</funding_grant_id><funding_grant_id>RCCFEL&amp;amp;#x2216</funding_grant_id><funding_grant_id>22759</funding_grant_id><funding_grant_id>MC_PC_17230</funding_grant_id><funding_grant_id>22145</funding_grant_id><funding_grant_id>-</funding_grant_id><funding_grant_id>MOH-001104</funding_grant_id><funding_grant_id>BRC-1215-20014</funding_grant_id><funding_grant_id>MOH-000715-00</funding_grant_id><funding_grant_id>203151/Z/16/Z</funding_grant_id><funding_grant_id>OF-LCG18May-0028</funding_grant_id><funding_grant_id>A25117</funding_grant_id><funding_grant_id>RCCFEL\100072</funding_grant_id><pubmed_authors>Jaynes P</pubmed_authors><pubmed_authors>Peng Y</pubmed_authors><pubmed_authors>Hoang PM</pubmed_authors><pubmed_authors>Chan EHL</pubmed_authors><pubmed_authors>Sridhar S</pubmed_authors><pubmed_authors>Chng WJ</pubmed_authors><pubmed_authors>De Mel S</pubmed_authors><pubmed_authors>Tan SY</pubmed_authors><pubmed_authors>Choi H</pubmed_authors><pubmed_authors>Moutsopoulos I</pubmed_authors><pubmed_authors>Lee J</pubmed_authors><pubmed_authors>Gay LJ</pubmed_authors><pubmed_authors>Ong CK</pubmed_authors><pubmed_authors>Ng SB</pubmed_authors><pubmed_authors>Khoury JD</pubmed_authors><pubmed_authors>Pitt JJ</pubmed_authors><pubmed_authors>Jeyasekharan AD</pubmed_authors><pubmed_authors>Hue SS</pubmed_authors><pubmed_authors>Chang ST</pubmed_authors><pubmed_authors>Bottos A</pubmed_authors><pubmed_authors>Scott DW</pubmed_authors><pubmed_authors>Chee YL</pubmed_authors><pubmed_authors>Tang T</pubmed_authors><pubmed_authors>Mohorianu I</pubmed_authors><pubmed_authors>Runge HFP</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Mottok A</pubmed_authors><pubmed_authors>Chuang SS</pubmed_authors><pubmed_authors>Tripodo C</pubmed_authors><pubmed_authors>Shuangyi F</pubmed_authors><pubmed_authors>Kannan K</pubmed_authors><pubmed_authors>Grigoropoulos NF</pubmed_authors><pubmed_authors>Hodson DJ</pubmed_authors><pubmed_authors>Liu CX</pubmed_authors><pubmed_authors>Nagarajan C</pubmed_authors><pubmed_authors>Kumar G</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Harris C</pubmed_authors><pubmed_authors>Poon L</pubmed_authors><pubmed_authors>Lim ST</pubmed_authors><pubmed_authors>Hoppe MM</pubmed_authors><pubmed_authors>Farinha P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Patterns of Oncogene Coexpression at Single-Cell Resolution Influence Survival in Lymphoma.</name><description>Cancers often overexpress multiple clinically relevant oncogenes, but it is not known if combinations of oncogenes in cellular subpopulations within a cancer influence clinical outcomes. Using quantitative multispectral imaging of the prognostically relevant oncogenes MYC, BCL2, and BCL6 in diffuse large B-cell lymphoma (DLBCL), we show that the percentage of cells with a unique combination MYC+BCL2+BCL6- (M+2+6-) consistently predicts survival across four independent cohorts (n = 449), an effect not observed with other combinations including M+2+6+. We show that the M+2+6- percentage can be mathematically derived from quantitative measurements of the individual oncogenes and correlates with survival in IHC (n = 316) and gene expression (n = 2,521) datasets. Comparative bulk/single-cell tr</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2026-05-29T01:13:23.667Z</modification><creation>2025-02-19T04:29:15.585Z</creation></dates><accession>S-EPMC10157367</accession><cross_references><pubmed>37071673</pubmed><doi>10.1158/2159-8290.CD-22-0998</doi></cross_references></HashMap>