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BCL10 gene mutations rarely occur in lymphoid malignancies

Authors :
Luca Baldini
Antonino Neri
Stefano Luminari
Anna Teresa Maiolo
Emanuele Zucca
L. Cro
Emilio Berti
Daniela Intini
Franco Cavalli
Francesco Bertoni
Luminari, S
Intini, D
Baldini, L
Berti, E
Bertoni, F
Zucca, E
Cro, L
Maiolo, A
Cavalli, F
Neri, A
Source :
Scopus-Elsevier, Università degli studi di Modena e Reggio Emilia-IRIS
Publication Year :
2000

Abstract

BCL10, a gene involved in apoptosis signalling, has recently been identified through the cloning of chromosomal breakpoints in extranodal (MALT-type) marginal zone lymphomas carrying the t(1;14)(p22;q32) translocation. BCL10 was also found mutated in these cases as well as in other types of lymphoid and solid tumors, suggesting that its inactivation may play an important pathogenetic role; however, this has been questioned by recent studies showing a lack of somatic mutations in human cancers. We report the mutation analysis of exons 1‐3 of the BCL10 gene in DNAs from 228 cases of lymphoid malignancies (30 B cell chronic lymphocytic leukemias, 123 B and 45 T non-Hodgkin’s lymphomas and 30 multiple myelomas). Somatic mutations were detected in four cases (

Details

ISSN :
08876924
Volume :
14
Issue :
5
Database :
OpenAIRE
Journal :
Leukemia
Accession number :
edsair.doi.dedup.....504eeb486707dc30f1065207a0a626c5