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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1998-9-15
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pubmed:abstractText |
The chromosomal translocation t(11;14)(q13;q32) is the hallmark of mantle cell lymphoma (MCL) in which it can be detected cytogenetically in about 75% of cases. The t(11;14) translocation juxtaposes the bcl-1 locus in chromosome band 11q13 next to the IgH locus in chromosome band 14q32 and, thus, leads to deregulation of the cell cycle regulatory protein cyclin D1, which is encoded by the CCND1 gene localized at the telomeric border of the bcl-1-locus. MCL has the worst prognosis of all low-grade non-Hodgkin's lymphomas (NHL). In some instances, however, histopathologic differentiation between MCL and other low-grade B-cell NHL is difficult. Therefore, detection of the t(11;14) translocation is of essential diagnostic value for the risk-adjusted management of patients with MCL. Unfortunately, chromosome analyses are frequently hampered by the low yield and quality of tumor metaphases. As the 11q13 breakpoints are scattered over a region of more than 120 kb the application of molecular genetic techniques is also limited.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0923-7534
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pubmed:author |
pubmed-author:BorowskiAA,
pubmed-author:GroteWW,
pubmed-author:HarderSS,
pubmed-author:KhawA HAH,
pubmed-author:MatthiesenPP,
pubmed-author:MetzkeSS,
pubmed-author:PlendlHH,
pubmed-author:RoggeroEE,
pubmed-author:SchlegelbergerBB,
pubmed-author:SiebertRR,
pubmed-author:Weber-MatthiesenKK,
pubmed-author:Zühlke-JenischRR,
pubmed-author:ZhangYY,
pubmed-author:ZuccaEE
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pubmed:issnType |
Print
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
519-26
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:9653493-Aged,
pubmed-meshheading:9653493-Chromosomes, Human, Pair 11,
pubmed-meshheading:9653493-Chromosomes, Human, Pair 14,
pubmed-meshheading:9653493-Female,
pubmed-meshheading:9653493-Humans,
pubmed-meshheading:9653493-In Situ Hybridization, Fluorescence,
pubmed-meshheading:9653493-Lymphoma, Non-Hodgkin,
pubmed-meshheading:9653493-Male,
pubmed-meshheading:9653493-Middle Aged,
pubmed-meshheading:9653493-Translocation, Genetic
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pubmed:year |
1998
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pubmed:articleTitle |
Application of interphase cytogenetics for the detection of t(11;14)(q13;q32) in mantle cell lymphomas.
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pubmed:affiliation |
Department of Human Genetics, University of Kiel, Germany. office@medgen.uni-kiel.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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