<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Klasener K</submitter><funding>Stiftelserna Wilhelm och Martina Lundgrens</funding><funding>Vetenskapsrådet</funding><funding>Swedish Cancer Foundation</funding><funding>Stiftelsen Apotekare Hedbergs Fond för Medicinsk Forskning</funding><funding>Roche Innovation Center Zurich</funding><funding>Barncancerfonden</funding><funding>Kungl. Vetenskaps- och Vitterhets-Samhället i Göteborg</funding><funding>IngaBritt och Arne Lundbergs Forskningsstiftelse</funding><funding>Åke Wiberg Stiftelse</funding><funding>Adlerbertska Research Foundation</funding><funding>Reumatikerförbundet</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>Stiftelsen Assar Gabrielssons Fond</funding><pagination>e70011</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11447455</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(10)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>Paediatric Burkitt's lymphoma (pBL) is the most common childhood non-Hodgkin B-cell lymphoma. Despite the encouraging survival rates for most children, treating cases with relapse/resistance to current therapies remains challenging. CD38 is a transmembrane protein highly expressed in pBL. This study investigates the effectiveness of CD38-targeting monoclonal antibodies (mAbs), daratumumab and isatuximab, in impairing crucial cellular processes and survival pathways in pBL malignant cells.&lt;h4>Methods&lt;/h4>&lt;i>In silico&lt;/i> analyses of patient samples, combined with &lt;i>in vitro&lt;/i> experiments using the Ramos cell line, were conducted to assess the impact of daratumumab and isatuximab on cellular proliferation, apoptosis and the phosphoinositide 3-kinase (PI3K) pathway.&lt;h4>R</pubmed_abstract><journal>Clinical &amp; translational immunology</journal><pubmed_title>Targeting CD38 with monoclonal antibodies disrupts key survival pathways in paediatric Burkitt's lymphoma malignant B cells.</pubmed_title><pmcid>PMC11447455</pmcid><funding_grant_id>BGR23‐03</funding_grant_id><funding_grant_id>19 0464</funding_grant_id><funding_grant_id>FB21‐104</funding_grant_id><funding_grant_id>2018‐03128</funding_grant_id><funding_grant_id>PR2020‐0147</funding_grant_id><funding_grant_id>FB22‐70</funding_grant_id><funding_grant_id>PR2018‐0170</funding_grant_id><pubmed_authors>Herrmann N</pubmed_authors><pubmed_authors>Boren J</pubmed_authors><pubmed_authors>Visentini M</pubmed_authors><pubmed_authors>Lundqvist C</pubmed_authors><pubmed_authors>Reth M</pubmed_authors><pubmed_authors>Camponeschi A</pubmed_authors><pubmed_authors>Aranburu A</pubmed_authors><pubmed_authors>Klasener K</pubmed_authors><pubmed_authors>Sundell T</pubmed_authors><pubmed_authors>Manna PT</pubmed_authors><pubmed_authors>Forsman H</pubmed_authors><pubmed_authors>Fogelstrand L</pubmed_authors><pubmed_authors>Martensson IL</pubmed_authors><pubmed_authors>Ljung Sass D</pubmed_authors><pubmed_authors>Jonsson CA</pubmed_authors><pubmed_authors>Sundqvist M</pubmed_authors><pubmed_authors>Mellgren K</pubmed_authors><pubmed_authors>Gjertsson I</pubmed_authors><pubmed_authors>Grimstad K</pubmed_authors><pubmed_authors>Ekwall O</pubmed_authors><pubmed_authors>Haversen L</pubmed_authors><pubmed_authors>McGrath S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeting CD38 with monoclonal antibodies disrupts key survival pathways in paediatric Burkitt's lymphoma malignant B cells.</name><description>&lt;h4>Objectives&lt;/h4>Paediatric Burkitt's lymphoma (pBL) is the most common childhood non-Hodgkin B-cell lymphoma. Despite the encouraging survival rates for most children, treating cases with relapse/resistance to current therapies remains challenging. CD38 is a transmembrane protein highly expressed in pBL. This study investigates the effectiveness of CD38-targeting monoclonal antibodies (mAbs), daratumumab and isatuximab, in impairing crucial cellular processes and survival pathways in pBL malignant cells.&lt;h4>Methods&lt;/h4>&lt;i>In silico&lt;/i> analyses of patient samples, combined with &lt;i>in vitro&lt;/i> experiments using the Ramos cell line, were conducted to assess the impact of daratumumab and isatuximab on cellular proliferation, apoptosis and the phosphoinositide 3-kinase (PI3K) pathway.&lt;h4>R</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2026-06-14T05:21:06.946Z</modification><creation>2025-04-04T02:30:03.751Z</creation></dates><accession>S-EPMC11447455</accession><cross_references><pubmed>39364393</pubmed><doi>10.1002/cti2.70011</doi></cross_references></HashMap>