Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1992-8-31
pubmed:abstractText
The chromosomal translocation t(15;17)(q22:21) of acute promyelocytic leukemia (APL) fuses PML, a novel gene, with RAR alpha, a retinoic acid receptor gene. PML-RAR hybrid transcripts were studied in 18 cases of APL using RNA-PCR. Two forms were noted: one designated 5', producing a 439-bp chimeric fragment, and a 3' form, producing a pair of fragments of 765 bp and 909 bp. 5' forms were found in 7 of the 18 cases while the other 11 patients expressed the 3' forms. The chromosome 15 specific probes K3 and K2 were used to study genomic breakpoints in 12 APL patients. Comparison of these results with RNA PCR in 11 patients for whom both were available yielded a rearrangement pattern predictive of whether the hybrid transcript was 5' or 3'. In this way, an additional three patients in whom DNA but not RNA was available were identified as having 3' (downstream) breakpoints and, therefore, 3' hybrid forms. Thus, 21 cases categorized as having 5' or 3' PML-RAR transcripts were analyzed for various phenotypic differences. Surface phenotyping of leukemic promyelocytes demonstrated expression of the CD2 antigen in all cases with the 5' splice variant. Only 1 of 11 cases with the 3' form showed CD2 expression. This difference is significant at P = .001.
pubmed:grant
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0006-4971
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
80
pubmed:geneSymbol
PML
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
582-6
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:1353379-Adult, pubmed-meshheading:1353379-Antigens, CD, pubmed-meshheading:1353379-Antigens, CD2, pubmed-meshheading:1353379-Antigens, Differentiation, T-Lymphocyte, pubmed-meshheading:1353379-Blotting, Southern, pubmed-meshheading:1353379-Bone Marrow, pubmed-meshheading:1353379-Carrier Proteins, pubmed-meshheading:1353379-Chromosome Aberrations, pubmed-meshheading:1353379-Chromosomes, Human, Pair 15, pubmed-meshheading:1353379-Chromosomes, Human, Pair 17, pubmed-meshheading:1353379-Cloning, Molecular, pubmed-meshheading:1353379-DNA, Neoplasm, pubmed-meshheading:1353379-Flow Cytometry, pubmed-meshheading:1353379-Humans, pubmed-meshheading:1353379-Immunophenotyping, pubmed-meshheading:1353379-Karyotyping, pubmed-meshheading:1353379-Leukemia, Promyelocytic, Acute, pubmed-meshheading:1353379-Polymerase Chain Reaction, pubmed-meshheading:1353379-Receptors, Immunologic, pubmed-meshheading:1353379-Receptors, Retinoic Acid, pubmed-meshheading:1353379-Restriction Mapping, pubmed-meshheading:1353379-T-Lymphocytes, pubmed-meshheading:1353379-Transcription, Genetic, pubmed-meshheading:1353379-Translocation, Genetic, pubmed-meshheading:1353379-Tretinoin
pubmed:year
1992
pubmed:articleTitle
Correlation of CD2 expression with PML gene breakpoints in patients with acute promyelocytic leukemia.
pubmed:affiliation
Department of Hematology, University of Texas M.D. Anderson Cancer Center, Houston 77030.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't