<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(9)</volume><submitter>Chen D</submitter><pubmed_abstract>Precursor-B cell receptor (pre-BCR) signaling represents a crucial checkpoint at the pre-B cell stage. Aberrant pre-BCR signaling is considered as a key factor for B-cell precursor acute lymphoblastic leukemia (BCP-ALL) development. BCP-ALL are believed to be arrested at the pre-BCR checkpoint independent of pre-BCR expression. However, the cellular stage at which BCP-ALL are arrested and whether this relates to expression of the pre-BCR components (IGHM, IGLL1 and VPREB1) is still unclear. Here, we show differential protein expression and copy number variation (CNV) patterns of the pre-BCR components in pediatric BCP-ALL. Moreover, analyzing six BCP-ALL data sets (n = 733), we demonstrate that TCF3-PBX1 ALL express high levels of IGHM, IGLL1 and VPREB1, and are arrested at the pre-B stage</pubmed_abstract><journal>PloS one</journal><pagination>e0162638</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5017602</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The Expression Pattern of the Pre-B Cell Receptor Components Correlates with Cellular Stage and Clinical Outcome in Acute Lymphoblastic Leukemia.</pubmed_title><pmcid>PMC5017602</pmcid><pubmed_authors>Abrahamsson J</pubmed_authors><pubmed_authors>Zheng J</pubmed_authors><pubmed_authors>Gerasimcik N</pubmed_authors><pubmed_authors>Lagerstedt K</pubmed_authors><pubmed_authors>Fogelstrand L</pubmed_authors><pubmed_authors>Martensson IL</pubmed_authors><pubmed_authors>Sjogren H</pubmed_authors><pubmed_authors>Chen D</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Expression Pattern of the Pre-B Cell Receptor Components Correlates with Cellular Stage and Clinical Outcome in Acute Lymphoblastic Leukemia.</name><description>Precursor-B cell receptor (pre-BCR) signaling represents a crucial checkpoint at the pre-B cell stage. Aberrant pre-BCR signaling is considered as a key factor for B-cell precursor acute lymphoblastic leukemia (BCP-ALL) development. BCP-ALL are believed to be arrested at the pre-BCR checkpoint independent of pre-BCR expression. However, the cellular stage at which BCP-ALL are arrested and whether this relates to expression of the pre-BCR components (IGHM, IGLL1 and VPREB1) is still unclear. Here, we show differential protein expression and copy number variation (CNV) patterns of the pre-BCR components in pediatric BCP-ALL. Moreover, analyzing six BCP-ALL data sets (n = 733), we demonstrate that TCF3-PBX1 ALL express high levels of IGHM, IGLL1 and VPREB1, and are arrested at the pre-B stage</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016</publication><modification>2026-05-05T15:49:14.03Z</modification><creation>2019-03-26T22:48:06Z</creation></dates><accession>S-EPMC5017602</accession><cross_references><pubmed>27611867</pubmed><doi>10.1371/journal.pone.0162638</doi></cross_references></HashMap>