<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Espinet B</submitter><funding>NIAID NIH HHS</funding><pagination>1007-19</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4488901</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(4)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>According to current diagnostic criteria, mantle cell lymphoma (MCL) encompasses the usual, aggressive variants and rare, nonnodal cases with monoclonal asymptomatic lymphocytosis, cyclin D1-positive (MALD1). We aimed to understand the biology behind this clinical heterogeneity and to identify markers for adequate identification of MALD1 cases.&lt;h4>Experimental design&lt;/h4>We compared 17 typical MCL cases with a homogeneous group of 13 untreated MALD1 cases (median follow-up, 71 months). We conducted gene expression profiling with functional analysis in five MCL and five MALD1. Results were validated in 12 MCL and 8 MALD1 additional cases by quantitative reverse transcription polymerase chain reaction (qRT-PCR) and in 24 MCL and 13 MALD1 cases by flow cytometry. Classificatio</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>Distinction between asymptomatic monoclonal B-cell lymphocytosis with cyclin D1 overexpression and mantle cell lymphoma: from molecular profiling to flow cytometry.</pubmed_title><pmcid>PMC4488901</pmcid><funding_grant_id>R01 AI057653</funding_grant_id><pubmed_authors>Serrano S</pubmed_authors><pubmed_authors>Ferrer A</pubmed_authors><pubmed_authors>Sanz F</pubmed_authors><pubmed_authors>Bellosillo B</pubmed_authors><pubmed_authors>Orfao A</pubmed_authors><pubmed_authors>Navarro JT</pubmed_authors><pubmed_authors>Garcia-Garcia M</pubmed_authors><pubmed_authors>Florensa L</pubmed_authors><pubmed_authors>Salar A</pubmed_authors><pubmed_authors>Luno E</pubmed_authors><pubmed_authors>Gimeno J</pubmed_authors><pubmed_authors>Nonell L</pubmed_authors><pubmed_authors>Abrisqueta P</pubmed_authors><pubmed_authors>Cerutti A</pubmed_authors><pubmed_authors>Espinet B</pubmed_authors><pubmed_authors>Lloreta J</pubmed_authors><pubmed_authors>Dominguez-Sola D</pubmed_authors><pubmed_authors>Sole F</pubmed_authors><pubmed_authors>Minana B</pubmed_authors><pubmed_authors>de la Banda E</pubmed_authors><pubmed_authors>Arenillas L</pubmed_authors><pubmed_authors>Collado R</pubmed_authors><pubmed_authors>Serrano C</pubmed_authors><pubmed_authors>Fernandez-Rodriguez C</pubmed_authors><pubmed_authors>Puigdecanet E</pubmed_authors><pubmed_authors>Vela MC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Distinction between asymptomatic monoclonal B-cell lymphocytosis with cyclin D1 overexpression and mantle cell lymphoma: from molecular profiling to flow cytometry.</name><description>&lt;h4>Purpose&lt;/h4>According to current diagnostic criteria, mantle cell lymphoma (MCL) encompasses the usual, aggressive variants and rare, nonnodal cases with monoclonal asymptomatic lymphocytosis, cyclin D1-positive (MALD1). We aimed to understand the biology behind this clinical heterogeneity and to identify markers for adequate identification of MALD1 cases.&lt;h4>Experimental design&lt;/h4>We compared 17 typical MCL cases with a homogeneous group of 13 untreated MALD1 cases (median follow-up, 71 months). We conducted gene expression profiling with functional analysis in five MCL and five MALD1. Results were validated in 12 MCL and 8 MALD1 additional cases by quantitative reverse transcription polymerase chain reaction (qRT-PCR) and in 24 MCL and 13 MALD1 cases by flow cytometry. Classificatio</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Feb</publication><modification>2026-05-30T13:42:18.62Z</modification><creation>2026-04-08T07:20:07.692Z</creation></dates><accession>S-EPMC4488901</accession><cross_references><pubmed>24352646</pubmed><doi>10.1158/1078-0432.CCR-13-1077</doi><doi>10.1158/1078-0432.ccr-13-1077</doi></cross_references></HashMap>