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PMID: 12124346 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Alternative translocation breakpoint cluster region 5' to BCL-6 in B-cell non-Hodgkin's lymphoma.

Cancer research ·Vol. 62 ·No. 14 ·2002-07-15 ·Pages 4089-94

Butler MP, Iida S, Capello D, Rossi D, Rao PH, Nallasivam P, Louie DC, Chaganti S, Au T, Gascoyne RD, Gaidano G, Chaganti RS, Dalla-Favera R

Abstract

Chromosomal translocations involving band 3q27 with various different partner chromosomes represent a recurrent cytogenetic abnormality in B-cell non-Hodgkin's lymphoma. In a fraction of these translocations, the chromosomal breakpoint is located within the 5' noncoding region of the BCL-6 proto-oncogene where the BCL-6 major breakpoint region (MBR) maps. As a result of the translocation, BCL-6 expression is deregulated by promoter substitution. However, between 30 and 50% of lymphomas with cytogenetically detectable translocations affecting band 3q27 retain a germ-line configuration at the BCL-6 locus. To identify possible additional breakpoint clusters within 3q27, we cloned a t(3;14)(q27;q32) lymphoma without MBR rearrangement and found a novel breakpoint site located between 245 and 285 kb 5' to BCL-6. Breakpoints within this newly described region, which we called the alternative breakpoint region (ABR), were found to be recurrent in lymphomas carrying t(3q27) chromosomal translocations but devoid of BCL-6 MBR rearrangements. Comparative analysis of multiple lymphomas carrying rearrangements within the ABR showed that the breakpoints cluster within a 20-kb distance. Translocations involving the ABR may juxtapose BCL-6 to distantly acting, heterologous transcriptional regulatory elements which cause deregulation of the proto-oncogene. The identification of BCL-6 ABR provides new tools for the diagnosis of lymphomas carrying aberrations at 3q27 and deregulated BCL-6 genes.

MeSH Terms
Base Sequence Chromosome Breakage Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 3 Cloning, Molecular DNA-Binding Proteins/genetics Gene Expression Regulation, Neoplastic/genetics Humans Lymphoma, B-Cell/genetics Molecular Sequence Data Proto-Oncogene Mas Proto-Oncogene Proteins/genetics Proto-Oncogene Proteins c-bcl-6 Transcription Factors/genetics Translocation, Genetic
Chemicals
DNA-Binding Proteins MAS1 protein, human Proto-Oncogene Mas Proto-Oncogene Proteins Proto-Oncogene Proteins c-bcl-6 Transcription Factors
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Butler Marion P
Institute for Cancer Genetics, and the Department of Pathology, Columbia University, New York, NY 10032, USA.
Iida Shinsuke
Capello Daniela
Rossi Davide
Rao Pulivarthi H
Nallasivam Palanisamy
Louie Diane C
Chaganti Seeta
Au Thomas
Gascoyne Randy D
Gaidano Gianluca
Chaganti Raju S K
Dalla-Favera Riccardo
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
2002-07-15
Pages
4089-94
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NCI NIH HHS · CA-37295 · United States
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