Document Detail

Characterization of t(2;5) reciprocal transcripts and genomic breakpoints in CD30+ cutaneous lymphoproliferations.
MedLine Citation:
PMID:  9616164     Owner:  NLM     Status:  MEDLINE    
NPM-ALK chimeric transcripts, encoded by the t(2;5), lead to an aberrant expression of ALK by CD30+ systemic lymphomas. To determine if t(2;5) is involved in cutaneous lymphoproliferative disorders, we studied 37 CD30+ cutaneous lymphoproliferations, 27 mycosis fungoides (MF), and 16 benign inflammatory disorders (BID). NPM-ALK transcripts were detected by nested reverse transcription-polymerase chain reaction (RT-PCR) in 1 of 11 lymphomatoid papulosis (LyP), 7 of 15 CD30+ primary cutaneous T-cell lymphoma (CTCL), 3 of 11 CD30+ secondary cutaneous lymphoma, 6 of 27 MF, and 1 of 16 BID. However, the expression of NPM-ALK transcripts was not associated with ALK1 immunoreactivity in MF, LyP, or BID cases. Only 1 CD30+ primary CTCL and 3 CD30+ secondary cutaneous lymphoma were ALK1 immunoreactive. The ALK1+ cases were also characterized by amplification of tumor-specific genomic breakpoints on derivative chromosome 5. These cases, except for 1 secondary cutaneous lymphoma, were also characterized by reciprocal breakpoints on derivative chromosome 2, leading to the expression of reciprocal ALK-NPM transcripts. Amplification of chromosomal breakpoints on both derivative chromosomes could represent an alternative to conventional cytogenetics for the diagnosis of t(2;5) and seems to be more reliable than the detection of cryptic NPM-ALK transcripts by nested RT-PCR.
M Beylot-Barry; A Groppi; B Vergier; K Pulford; J P Merlio
Related Documents :
16101124 - Characterization of igh rearrangements in non-hodgkin's b-cell lymphomas by fluorescenc...
7923064 - "jumping" translocation of 9q in a case of follicular lymphoma.
12930384 - Multicolour fluorescence in situ hybridization analysis of t(14;18)-positive follicular...
1766674 - Bcl-2/jh rearrangements in benign lymphoid tissues with follicular hyperplasia.
8640474 - Allelic deletion mapping of putative tumor suppressor genes on 17q in sporadic ovarian ...
2900604 - Spontaneous mutation in the male gamete as a cause of hemophilia a: clarification of a ...
Publication Detail:
Type:  Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Blood     Volume:  91     ISSN:  0006-4971     ISO Abbreviation:  Blood     Publication Date:  1998 Jun 
Date Detail:
Created Date:  1998-06-30     Completed Date:  1998-06-30     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  7603509     Medline TA:  Blood     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  4668-76     Citation Subset:  AIM; IM    
CHU of Bordeaux and University of Bordeaux II, Bordeaux, France.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Antigens, CD30
Base Sequence
Chromosomes, Human, Pair 2*
Chromosomes, Human, Pair 5*
Genome, Human*
Lymphoproliferative Disorders / genetics*
Molecular Sequence Data
Skin Diseases / genetics*
Translocation, Genetic*
Reg. No./Substance:
0/Antigens, CD30

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  MLL and CALM are fused to AF10 in morphologically distinct subsets of acute leukemia with translocat...
Next Document:  Homozygous deletions at chromosome 9p21 involving p16 and p15 are associated with histologic progres...