Fluorescent in situ hybridization for the detection of t(8:14) in Burkitt's lymphoma

Burkitt's lymphoma cells exhibit the reciprocal balanced chromosomal translocation t(8:14) in 75% of patients. Cytogenetic analysis is time-consuming, requires in vitro culture with mitogens and enables to analyse a relatively small number of cells. We evaluated the role of multicolor fluoresce...

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Bibliographic Details
Published in:Acta haematologica Vol. 90; no. 4; p. 186
Main Authors: Lishner, M, Kenet, G, Lalkin, A, Yarkoni, S, Ben-Bassat, H, Fejgin, M, Rechavi, G, Amiel, A
Format: Journal Article
Language:English
Published: Switzerland 01-01-1993
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Summary:Burkitt's lymphoma cells exhibit the reciprocal balanced chromosomal translocation t(8:14) in 75% of patients. Cytogenetic analysis is time-consuming, requires in vitro culture with mitogens and enables to analyse a relatively small number of cells. We evaluated the role of multicolor fluorescent in situ hybridization (FISH) in the rapid detection of t(8:14) in Burkitt's lymphoma cells. FISH detected the JH/myc translocation in 100% of the cells of five cell lines carrying the classical t(8:14) and in fresh cells obtained from a newly diagnosed Burkitt's lymphoma patient. In contrast, the translocation was not detected in the Bajb cell line that does not carry t(8:14). We conclude that FISH is a rapid and reliable diagnostic tool for the detection of the JH/myc translocation in Burkitt's lymphoma patients.
ISSN:0001-5792
DOI:10.1159/000204455