Source:http://linkedlifedata.com/resource/pubmed/id/12800154
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2003-6-11
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pubmed:abstractText |
B-cell chronic lymphocytic leukemia (CLL) is not a uniform disease entity; approximately half of the CLL cases have undergone immunoglobulin V(H) gene hypermutation, whereas the other half display unmutated V(H) genes. We investigated genome changes in 12 hypermutated cases (M-CLL) and 22 unmutated cases (UM-CLL) by use of comparative genomic hybridization, G-banding, and multicolor fluorescence in situ hybridization (m-FISH) after optimal mitogen stimulation and FISH analysis of typical CLL aberrations: 11q deletion, 13q deletion, and trisomy 12. Very high frequencies of aberrations were found in both groups: 82% in UM-CLL and 83% in M-CLL. Deletions of 11q and 13q were equally distributed in M-CLL and UM-CLL. However, larger aberrations detectable by CGH, trisomy 12, and complex aberrations were less frequent in M-CLL than in UM-CLL. These observations led to a hypothesis that unmutated and mutated CLL have different biological Backgrounds, given that large and/or complex chromosomal aberrations and hypermutation of the CLL progenitor cells tend to be mutually exclusive.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1045-2257
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2003 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:volume |
37
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
417-20
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:12800154-Chromosome Aberrations,
pubmed-meshheading:12800154-Chromosome Deletion,
pubmed-meshheading:12800154-Female,
pubmed-meshheading:12800154-Gene Amplification,
pubmed-meshheading:12800154-Humans,
pubmed-meshheading:12800154-Immunoglobulin Heavy Chains,
pubmed-meshheading:12800154-Immunoglobulin Variable Region,
pubmed-meshheading:12800154-Karyotyping,
pubmed-meshheading:12800154-Leukemia, Lymphocytic, Chronic, B-Cell,
pubmed-meshheading:12800154-Male
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pubmed:year |
2003
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pubmed:articleTitle |
More extensive genetic alterations in unmutated than in hypermutated cases of chronic lymphocytic leukemia.
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pubmed:affiliation |
Laboratory of Cancer Genetics, University of Tampere and Tampere University Hospital, Tampere, Finland.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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