Source:http://linkedlifedata.com/resource/pubmed/id/10510675
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1999-10-19
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pubmed:abstractText |
We describe the usefulness of a real-time polymerase chain reaction (PCR) assay for detection of the t(11;14)(q13;q32), most commonly present in mantle cell lymphoma (MCL). This assay is based on the 5'-->3' exonuclease activity of Taq polymerase, which cleaves an internal probe labeled with a reporter dye at its 5' end and a quencher dye at its 3' end during PCR. The real-time t(11;14) PCR assay was established using DNA from a case of MCL with the t(11;14), amplifiable using conventional PCR and primers specific for the major translocation cluster (MTC) region of the bcl-1 locus and the immunoglobulin heavy chain joining region gene (JH). The specificity was determined by analyzing DNA from 82 cases: 50 MCL, 27 other types of non-Hodgkin lymphoma (NHL), and 5 reactive lymphoid proliferations. The real-time t(11;14) PCR results were correlated with data obtained by a conventional PCR assay. By using the real-time assay, bcl-1 MTC/JH DNA fusion sequences were detected in 25 of 50 MCLs but not in other NHLs or reactive lymphoid proliferations. Concordance between real-time and conventional PCR methods for MCL was 96% and for all samples was 98%. The results demonstrate that this real-time PCR method to detect bcl-1 MTC/JH DNA fusion sequences is specific and reliable. In addition, the results are available immediately following amplification, without standard post-PCR manipulations.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Exodeoxyribonuclease V,
http://linkedlifedata.com/resource/pubmed/chemical/Exodeoxyribonucleases,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Heavy Chains,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Joining Region,
http://linkedlifedata.com/resource/pubmed/chemical/Taq Polymerase
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0002-9173
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
112
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
524-30
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pubmed:dateRevised |
2005-11-17
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pubmed:meshHeading |
pubmed-meshheading:10510675-Chromosomes, Human, Pair 11,
pubmed-meshheading:10510675-Chromosomes, Human, Pair 14,
pubmed-meshheading:10510675-Computer Systems,
pubmed-meshheading:10510675-Exodeoxyribonuclease V,
pubmed-meshheading:10510675-Exodeoxyribonucleases,
pubmed-meshheading:10510675-Humans,
pubmed-meshheading:10510675-Immunoglobulin Heavy Chains,
pubmed-meshheading:10510675-Immunoglobulin Joining Region,
pubmed-meshheading:10510675-Lymphoma, Non-Hodgkin,
pubmed-meshheading:10510675-Polymerase Chain Reaction,
pubmed-meshheading:10510675-Taq Polymerase,
pubmed-meshheading:10510675-Translocation, Genetic
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pubmed:year |
1999
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pubmed:articleTitle |
Real-time 5'-->3' exonuclease-based PCR assay for detection of the t(11;14)(q13;q32).
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pubmed:affiliation |
Department of Pathology, University of Texas MD, Anderson Cancer Center, Houston 77030, USA.
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pubmed:publicationType |
Journal Article
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