Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1992-3-30
pubmed:abstractText
The present study provides immunobiochemical and molecular data on the differentiation-linked expression of the bcl-2 proto-oncogene in normal and neoplastic myeloid cells. Using a recently developed monoclonal antibody (MoAb) to the bcl-2 molecule, staining of normal bone marrow myeloblasts, promyelocytes, and myelocytes, but neither monocytes nor most polymorphonuclear cells, was demonstrated. By two-color flow cytometric analysis, bcl-2 was evidenced in CD33+ and CD33+/CD34+ myeloid cells as well as in the more primitive CD33-/CD34+ population. The leukemic cell lines HL-60, KG1, GM-1, and K562 were bcl-2 positive together with 11 of 14 acute myeloid leukemias (AML) and three of three chronic myeloid leukemias (CML) in blast crises; six of seven CML were negative. Among myelodysplastic cases, augmentation of the bcl-2 positive myeloblastic compartment was found in refractory anemia with excess of blasts (RAEB) and in transformation (RAEB-t). Western blots of myeloid leukemias and control lymphocytes extracts evidenced an anti-bcl-2 immunoreactive band of the expected size (26 Kd). Moreover, the HL-60 and KG1 cell lines, both positive for the bcl-2 protein, exhibited the appropriate size bcl-2 mRNA (7.5 Kb). These findings clearly indicate that the bcl-2 gene is operative in myeloid cells and that the anti-bcl-2 MoAb identifies its product and not a cross-reactive epitope. Induction of HL-60 differentiation toward the monocytic and granulocytic pathways was accompanied by a marked decrease in bcl-2 mRNA and protein levels; bivariate flow cytometric analysis showed that the fraction becoming bcl-2 negative was in the G1 phase of the cell cycle. These data establish that the bcl-2 proto-oncogene is expressed on myeloid cells and their progenitors and is regulated in a differentiation-linked manner.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0006-4971
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
79
pubmed:geneSymbol
bcl-2
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1291-8
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:1536952-Anemia, Refractory, with Excess of Blasts, pubmed-meshheading:1536952-Blotting, Western, pubmed-meshheading:1536952-Bone Marrow, pubmed-meshheading:1536952-Cell Differentiation, pubmed-meshheading:1536952-Flow Cytometry, pubmed-meshheading:1536952-Gene Expression, pubmed-meshheading:1536952-Gene Expression Regulation, Neoplastic, pubmed-meshheading:1536952-Granulocytes, pubmed-meshheading:1536952-Humans, pubmed-meshheading:1536952-Immunohistochemistry, pubmed-meshheading:1536952-Leukemia, pubmed-meshheading:1536952-Leukemia, Myelogenous, Chronic, BCR-ABL Positive, pubmed-meshheading:1536952-Leukemia, Myeloid, Acute, pubmed-meshheading:1536952-Leukemia, Promyelocytic, Acute, pubmed-meshheading:1536952-Proto-Oncogene Proteins, pubmed-meshheading:1536952-Proto-Oncogene Proteins c-bcl-2, pubmed-meshheading:1536952-RNA, Messenger, pubmed-meshheading:1536952-Tumor Cells, Cultured
pubmed:year
1992
pubmed:articleTitle
bcl-2 proto-oncogene expression in normal and neoplastic human myeloid cells.
pubmed:affiliation
Istituto Nazionale per Lo Studio e La Cura Dei Tumori, Milan, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't