<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Winter SS</submitter><funding>NCI NIH HHS</funding><pagination>585-589</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8791581</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(2)</volume><pubmed_abstract>Immunotherapies directed against B-cell surface markers have been a common developmental strategy to treat B-cell malignancies. The immunoglobulin heavy chain surrogate light chain (SLC), comprising the VpreB1 (CD179a) and Lamda5 (CD179b) subunits, is expressed on pro- and pre-B cells, where it governs pre-B-cell receptor (BCR)-mediated autonomous survival signaling. We hypothesized that the pre-BCR might merit the development of targeted immunotherapies to decouple "autonomous" signaling in B-lineage acute lymphoblastic leukemia (B-ALL). We used the Children's Oncology Group (COG) minimal residual disease (MRD) flow panel to assess pre-BCR expression in 36 primary patient samples accrued to COG standard- and high-risk B-ALL studies through AALL03B1. We also assessed CD179a expression in 1</pubmed_abstract><journal>Blood advances</journal><pubmed_title>VpreB surrogate light chain expression in B-lineage ALL: a report from the Children's Oncology Group.</pubmed_title><pmcid>PMC8791581</pmcid><funding_grant_id>P30 CA021765</funding_grant_id><funding_grant_id>U10 CA180886</funding_grant_id><funding_grant_id>R35 CA197695</funding_grant_id><funding_grant_id>U10 CA180899</funding_grant_id><funding_grant_id>U24 CA196173</funding_grant_id><pubmed_authors>Qu C</pubmed_authors><pubmed_authors>Wilson BS</pubmed_authors><pubmed_authors>Carroll AJ</pubmed_authors><pubmed_authors>Mullighan CG</pubmed_authors><pubmed_authors>Simeona N</pubmed_authors><pubmed_authors>Winter SS</pubmed_authors><pubmed_authors>Heerema NA</pubmed_authors><pubmed_authors>Gheorghe G</pubmed_authors><pubmed_authors>McCaustland A</pubmed_authors><pubmed_authors>Wood BL</pubmed_authors></additional><is_claimable>false</is_claimable><name>VpreB surrogate light chain expression in B-lineage ALL: a report from the Children's Oncology Group.</name><description>Immunotherapies directed against B-cell surface markers have been a common developmental strategy to treat B-cell malignancies. The immunoglobulin heavy chain surrogate light chain (SLC), comprising the VpreB1 (CD179a) and Lamda5 (CD179b) subunits, is expressed on pro- and pre-B cells, where it governs pre-B-cell receptor (BCR)-mediated autonomous survival signaling. We hypothesized that the pre-BCR might merit the development of targeted immunotherapies to decouple "autonomous" signaling in B-lineage acute lymphoblastic leukemia (B-ALL). We used the Children's Oncology Group (COG) minimal residual disease (MRD) flow panel to assess pre-BCR expression in 36 primary patient samples accrued to COG standard- and high-risk B-ALL studies through AALL03B1. We also assessed CD179a expression in 1</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2026-05-28T23:33:44.508Z</modification><creation>2022-02-11T15:57:22.864Z</creation></dates><accession>S-EPMC8791581</accession><cross_references><pubmed>34662891</pubmed><doi>10.1182/bloodadvances.2021005245</doi></cross_references></HashMap>