Literature DB >> 6609313

Inversion of chromosome 14 marks human T-cell chronic lymphocytic leukaemia.

L Zech, G Gahrton, L Hammarström, G Juliusson, H Mellstedt, K H Robèrt, C I Smith.   

Abstract

Rare cases of chronic lymphocytic leukaemia (CLL) in man stem from the malignant proliferation of T cells. The disease is usually more aggressive clinically than B-cell-derived CLL. Various haematological tumours are associated with specific chromosome aberrations (for example, refs 1, 2). Only limited numbers of T-cell CLL patients have so far been studied cytogenetically and, whereas chromosome 12 seems particularly to be involved in B-cell CLL, several markers have been found in T-cell tumours. Recently, by stimulating malignant clones with different mitogens, novel chromosome abnormalities have been detected in T-cell CLL. Using the same approach for additional cases of T-cell CLL, we now report that the most consistent chromosome change is an inversion of the long arm of chromosome 14, inv(14)(q11 q32), in four of five patients. Another remarkable chromosome aberration is trisomy for the long arm of chromosome 8, found in three of five patients.

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Mesh:

Year:  1984        PMID: 6609313     DOI: 10.1038/308858a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  36 in total

1.  Mantle cell lymphoma is characterized by inactivation of the ATM gene.

Authors:  C Schaffner; I Idler; S Stilgenbauer; H Döhner; P Lichter
Journal:  Proc Natl Acad Sci U S A       Date:  2000-03-14       Impact factor: 11.205

2.  Small cell variant of T-cell prolymphocytic leukemia with a gammadelta immunophenotype.

Authors:  Shigeo Toyota; Norihiko Nakamura; Kazuo Dan
Journal:  Int J Hematol       Date:  2005-01       Impact factor: 2.490

Review 3.  T-cell clones and T-cell receptors.

Authors:  F W Fitch
Journal:  Microbiol Rev       Date:  1986-03

4.  Mammalian T-lymphocyte antigen receptor genes: genetic and nongenetic potential to generate variability.

Authors:  J T Epplen; J Chluba; C Hardt; A Hinkkanen; V Steimle; H Stockinger
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132

5.  Tissue specificity of chromosomal rearrangements in ataxia-telangiectasia.

Authors:  T L Kojis; R R Schreck; R A Gatti; R S Sparkes
Journal:  Hum Genet       Date:  1989-11       Impact factor: 4.132

6.  Nucleotide sequence of both reciprocal translocation junction regions in a patient with Ph positive acute lymphoblastic leukaemia, with a breakpoint within the first intron of the BCR gene.

Authors:  M J van der Feltz; M K Shivji; P B Allen; N Heisterkamp; J Groffen; L M Wiedemann
Journal:  Nucleic Acids Res       Date:  1989-01-11       Impact factor: 16.971

7.  New data on clonal anomalies of chromosome 14 in ataxia telangiectasia: tct(14;14) and inv(14).

Authors:  A Aurias; M F Croquette; J P Nuyts; C Griscelli; B Dutrillaux
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

8.  Sequence analysis of the MYC oncogene involved in the t(8;14)(q24;q11) chromosome translocation in a human leukemia T-cell line indicates that putative regulatory regions are not altered.

Authors:  S N Finver; K Nishikura; L R Finger; F G Haluska; J Finan; P C Nowell; C M Croce
Journal:  Proc Natl Acad Sci U S A       Date:  1988-05       Impact factor: 11.205

9.  Inv(14) with distal breakpoint in 14q32.1 in three cases of T cell lymphoma.

Authors:  B Schlegelberger; A C Feller; H H Wacker; J Lohmeyer; W Grote
Journal:  Hum Genet       Date:  1990-06       Impact factor: 4.132

10.  Molecular cloning of the breakpoint junction of a human chromosomal 8;14 translocation involving the T-cell receptor alpha-chain gene and sequences on the 3' side of MYC.

Authors:  T W McKeithan; E A Shima; M M Le Beau; J Minowada; J D Rowley; M O Diaz
Journal:  Proc Natl Acad Sci U S A       Date:  1986-09       Impact factor: 11.205

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