<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(1)</volume><submitter>Wang X</submitter><funding>Cancer Research Society</funding><funding>Terry Fox Research Institute</funding><funding>Genome British Columbia</funding><funding>Genome Canada</funding><funding>Gouvernement du Canada | Canadian Institutes of Health Research</funding><pubmed_abstract>Follicular lymphoma (FL) is an indolent cancer of mature B-cells but with ongoing risk of transformation to more aggressive histology over time. Recurrent mutations associated with transformation have been identified; however, prognostic features that can be discerned at diagnosis could be clinically useful. We present here comprehensive profiling of both tumor and immune compartments in 155 diagnostic FL biopsies at single-cell resolution by mass cytometry. This revealed a diversity of phenotypes but included two recurrent patterns, one which closely resembles germinal center B-cells (GCB) and another which appears more related to memory B-cells (MB). GCB-type tumors are enriched for EZH2, TNFRSF14, and MEF2B mutations, while MB-type tumors contain increased follicular helper T-cells. MB-</pubmed_abstract><journal>Nature communications</journal><pagination>6772</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9646774</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Single-cell profiling reveals a memory B cell-like subtype of follicular lymphoma with increased transformation risk.</pubmed_title><pmcid>PMC9646774</pmcid><pubmed_authors>May C</pubmed_authors><pubmed_authors>Shah SP</pubmed_authors><pubmed_authors>Islam R</pubmed_authors><pubmed_authors>Kim J</pubmed_authors><pubmed_authors>Morin RD</pubmed_authors><pubmed_authors>Sehn LH</pubmed_authors><pubmed_authors>Gracias D</pubmed_authors><pubmed_authors>Hilton L</pubmed_authors><pubmed_authors>Hirst M</pubmed_authors><pubmed_authors>Kusakabe M</pubmed_authors><pubmed_authors>Hung S</pubmed_authors><pubmed_authors>Scott DW</pubmed_authors><pubmed_authors>Aoki T</pubmed_authors><pubmed_authors>Nissen M</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Weng AP</pubmed_authors><pubmed_authors>Roth AJ</pubmed_authors><pubmed_authors>Simkin G</pubmed_authors><pubmed_authors>Wong R</pubmed_authors><pubmed_authors>Freeman C</pubmed_authors><pubmed_authors>Savage KJ</pubmed_authors><pubmed_authors>Chavez EA</pubmed_authors><pubmed_authors>Craig JW</pubmed_authors><pubmed_authors>Duns G</pubmed_authors><pubmed_authors>Segat GC</pubmed_authors><pubmed_authors>Tyshchenko K</pubmed_authors><pubmed_authors>Steidl C</pubmed_authors><pubmed_authors>Jiang A</pubmed_authors><pubmed_authors>Karsan A</pubmed_authors><pubmed_authors>Brinkman RR</pubmed_authors><pubmed_authors>Sarkozy C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-cell profiling reveals a memory B cell-like subtype of follicular lymphoma with increased transformation risk.</name><description>Follicular lymphoma (FL) is an indolent cancer of mature B-cells but with ongoing risk of transformation to more aggressive histology over time. Recurrent mutations associated with transformation have been identified; however, prognostic features that can be discerned at diagnosis could be clinically useful. We present here comprehensive profiling of both tumor and immune compartments in 155 diagnostic FL biopsies at single-cell resolution by mass cytometry. This revealed a diversity of phenotypes but included two recurrent patterns, one which closely resembles germinal center B-cells (GCB) and another which appears more related to memory B-cells (MB). GCB-type tumors are enriched for EZH2, TNFRSF14, and MEF2B mutations, while MB-type tumors contain increased follicular helper T-cells. MB-</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-04T09:02:44.965Z</modification><creation>2025-04-04T09:02:44.965Z</creation></dates><accession>S-EPMC9646774</accession><cross_references><pubmed>36351924</pubmed><doi>10.1038/s41467-022-34408-0</doi></cross_references></HashMap>