Source:http://linkedlifedata.com/resource/pubmed/id/11877310
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2002-3-5
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pubmed:abstractText |
Recent studies on the immunoglobulin variable heavy chain (IgV(H)) genes have revealed that B-cell chronic lymphocytic leukemia (B-CLL) consists of at least 2 clinical entities with either somatically mutated or unmutated V(H) genes. We have analyzed the V(H) gene mutation status and V(H) gene usage in 119 B-CLL cases and correlated them to overall survival. A novel finding was the preferential use of the V(H)3-21 gene in mutated cases, whereas biased V(H)1-69 gene usage was found in unmutated cases as previously reported. Interestingly, the subset of mutated cases using the V(H)3-21 gene displayed distinctive genotypic/phenotypic characteristics with shorter average length of the complementarity determining region 3 and clonal expression of lambda light chains. In addition, this mutated subset showed significantly shorter survival than other mutated cases and a similar clinical course to unmutated cases. We therefore suggest that B-CLL cases with mutated V(H)3-21 genes may constitute an additional entity of B-CLL.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0006-4971
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pubmed:author |
pubmed-author:BotlingJohanJ,
pubmed-author:EnbladGunillaG,
pubmed-author:HultdinMagnusM,
pubmed-author:JohnsonAnnaA,
pubmed-author:RoosGöranG,
pubmed-author:RosenquistRichardR,
pubmed-author:SällströmJanJ,
pubmed-author:SöderbergOlaO,
pubmed-author:SundströmChristerC,
pubmed-author:ThörnIngridI,
pubmed-author:ThunbergUlfU,
pubmed-author:TobinGerardG
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
99
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2262-4
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:11877310-Aged,
pubmed-meshheading:11877310-Complementarity Determining Regions,
pubmed-meshheading:11877310-Female,
pubmed-meshheading:11877310-Genes, Immunoglobulin,
pubmed-meshheading:11877310-Genetic Testing,
pubmed-meshheading:11877310-Genotype,
pubmed-meshheading:11877310-Humans,
pubmed-meshheading:11877310-Immunoglobulin lambda-Chains,
pubmed-meshheading:11877310-Leukemia, Lymphocytic, Chronic, B-Cell,
pubmed-meshheading:11877310-Male,
pubmed-meshheading:11877310-Mutation,
pubmed-meshheading:11877310-Phenotype,
pubmed-meshheading:11877310-Survival Rate
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pubmed:year |
2002
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pubmed:articleTitle |
Somatically mutated Ig V(H)3-21 genes characterize a new subset of chronic lymphocytic leukemia.
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pubmed:affiliation |
Department of Genetics and Pathology, Uppsala University, SE-751 85 Uppsala, Sweden.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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