CD2-positive B-cell precursor acute lymphoblastic leukemia with an early switch to the monocytic lineage
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, validační studie
PubMed
24270736
DOI
10.1038/leu.2013.354
PII: leu2013354
Knihovny.cz E-zdroje
- MeSH
- antigeny CD2 imunologie MeSH
- buněčný rodokmen MeSH
- dítě MeSH
- imunofenotypizace MeSH
- kohortové studie MeSH
- lidé MeSH
- mladiství MeSH
- monocyty patologie MeSH
- multiplexová polymerázová řetězová reakce MeSH
- pre-B-buněčná leukemie imunologie patologie MeSH
- předškolní dítě MeSH
- prognóza MeSH
- reziduální nádor MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- validační studie MeSH
- Názvy látek
- antigeny CD2 MeSH
Switches from the lymphoid to myeloid lineage during B-cell precursor acute lymphoblastic leukemia (BCP-ALL) treatment are considered rare and thus far have been detected in MLL-rearranged leukemia. Here, we describe a novel BCP-ALL subset, switching BCP-ALL or swALL, which demonstrated monocytosis early during treatment. Despite their monocytic phenotype, 'monocytoids' share immunoreceptor gene rearrangements with leukemic B lymphoblasts. All swALLs demonstrated BCP-ALL with CD2 positivity and no MLL alterations, and the proportion of swALLs cases among BCP-ALLs was unexpectedly high (4%). The upregulation of CEBPα and demethylation of the CEBPA gene were significant in blasts at diagnosis, prior to the time when most of the switching occurs. Intermediate stages between CD14(neg)CD19(pos)CD34(pos) B lymphoblasts and CD14(pos)CD19(neg)CD34(neg) 'monocytoids' were detected, and changes in the expression of PAX5, PU1, M-CSFR, GM-CSFR and other genes accompanied the switch. Alterations in the Ikaros and ERG genes were more frequent in swALL patients; however, both were altered in only a minority of swALLs. Moreover, switching could be recapitulated in vitro and in mouse xenografts. Although children with swALL respond slowly to initial therapy, risk-based ALL therapy appears the treatment of choice for swALL. SwALL shows that transdifferentiating into monocytic lineage is specifically associated with CEBPα changes and CD2 expression.
Department of Clinical Hematology University Hospital Motol Prague Czech Republic
Department of Pediatrics University Hospital Schleswig Holstein Kiel Germany
Northern Institute for Cancer Research Newcastle University Newcastle UK
University of Michigan Medical School Department of Pathology Ann Arbor MI USA
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