rdf:type |
|
lifeskim:mentions |
umls-concept:C0007589,
umls-concept:C0007600,
umls-concept:C0017287,
umls-concept:C0449450,
umls-concept:C0812385,
umls-concept:C1511938,
umls-concept:C1519595,
umls-concept:C1533691,
umls-concept:C1705535,
umls-concept:C1880022,
umls-concept:C1881379
|
pubmed:issue |
3-4
|
pubmed:dateCreated |
1994-6-2
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pubmed:abstractText |
A new Ph1-positive acute lymphoblastic leukemia cell line, designated as ALL/MIK, has been developed from a patient with Ph1-positive acute leukemia. The ALL/MIK cells showed an immunophenotype of common ALL with rearranged JH and Jk genes. The ALL/MIK cells showed no M-bcr rearrangement using Southern blot analysis with either 3' or 5' M-bcr probes, but had the bcr gene rearrangement on bcr-2 within the first intron of the bcr gene. Consistent with this result, the reverse transcriptase-dependent polymerase chain reaction (RT-PCR) assay revealed that the ALL/MIK cells contained the transcript derived fusion of the first exon of bcr gene and the second exon of abl gene. Although the ALL/MIK cells were defined as early pre-B cells by immunophenotypical and genotypical analyses, they were capable of differentiating into monocytoid lineage by when cultured with TPA. Furthermore, another Ph1-positive ALL cell line, (TOM-1), was investigated for its ability to differentiate to monocytoid lineage. TOM-1 was also induced to monocytoid lineage by TPA. Thus, the present study suggested that the leukemic transformation in some Ph1-positive ALL may occur at the level of multipotential hematopoietic cells capable of differentiating towards lymphoid and myelo-monocytoid lineage.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/BCR protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Neoplasm,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/Fusion Proteins, bcr-abl,
http://linkedlifedata.com/resource/pubmed/chemical/Oncogene Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Tyrosine Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-bcr,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Neoplasm
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1042-8194
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:volume |
12
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pubmed:geneSymbol |
bcr-2,
bcr-abl
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
N
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pubmed:pagination |
287-96
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:8167560-Aged,
pubmed-meshheading:8167560-Base Sequence,
pubmed-meshheading:8167560-Blotting, Northern,
pubmed-meshheading:8167560-Blotting, Southern,
pubmed-meshheading:8167560-Cell Differentiation,
pubmed-meshheading:8167560-Cell Line,
pubmed-meshheading:8167560-Culture Techniques,
pubmed-meshheading:8167560-DNA, Neoplasm,
pubmed-meshheading:8167560-DNA Primers,
pubmed-meshheading:8167560-Exons,
pubmed-meshheading:8167560-Female,
pubmed-meshheading:8167560-Fusion Proteins, bcr-abl,
pubmed-meshheading:8167560-Gene Expression,
pubmed-meshheading:8167560-Gene Rearrangement,
pubmed-meshheading:8167560-Genes, Immunoglobulin,
pubmed-meshheading:8167560-Humans,
pubmed-meshheading:8167560-Karyotyping,
pubmed-meshheading:8167560-Molecular Sequence Data,
pubmed-meshheading:8167560-Monocytes,
pubmed-meshheading:8167560-Oncogene Proteins,
pubmed-meshheading:8167560-Oncogenes,
pubmed-meshheading:8167560-Philadelphia Chromosome,
pubmed-meshheading:8167560-Polymerase Chain Reaction,
pubmed-meshheading:8167560-Precursor Cell Lymphoblastic Leukemia-Lymphoma,
pubmed-meshheading:8167560-Protein-Tyrosine Kinases,
pubmed-meshheading:8167560-Proto-Oncogene Proteins,
pubmed-meshheading:8167560-Proto-Oncogene Proteins c-bcr,
pubmed-meshheading:8167560-RNA, Neoplasm,
pubmed-meshheading:8167560-Restriction Mapping,
pubmed-meshheading:8167560-Transcription, Genetic,
pubmed-meshheading:8167560-Tumor Cells, Cultured
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pubmed:year |
1994
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pubmed:articleTitle |
Establishment and characterization of a new Ph1-positive ALL cell line (ALL/MIK) presenting bcr gene rearrangement on bcr-2 and ALL-type bcr/abl transcript: suggestion of in vitro differentiation to monocytoid lineage.
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pubmed:affiliation |
Third Department of Internal Medicine, Hokkaido University School of Medicine, Sapporo, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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