Bcl-2 molecular analysis in paraffin-embedded biopsies from diffuse large B-cell lymphomas

Citation
C. De Brasi et al., Bcl-2 molecular analysis in paraffin-embedded biopsies from diffuse large B-cell lymphomas, MEDICINA, 60(3), 2000, pp. 305-310
Citations number
26
Categorie Soggetti
Medical Research General Topics
Journal title
MEDICINA-BUENOS AIRES
ISSN journal
00257680 → ACNP
Volume
60
Issue
3
Year of publication
2000
Pages
305 - 310
Database
ISI
SICI code
0025-7680(2000)60:3<305:BMAIPB>2.0.ZU;2-Q
Abstract
Translocation t(14; 18) has been observed in 50-85% of follicular and in 30 % of diffuse non-Hodgkin lymphomas. About half of follicle center lymphoma (FCL) undergo histological conversion at relapse to more aggressive diffuse large B-cell lymphoma (DLBCL). This report correlates the molecular bcl-2/ lgH rearrangement by PCR and Bcl-2 immunohistochemical (IHC) expression in a series of high grade DLBCLs with and without FCL remnant. Twenty-three pa raffin-embedded lymph nodes from DLBCL patients were analyzed. Eleven patie nts showed FCL remnant (Group A) and 12, did not (Group B). Single PCR from paraffin extracted DNA followed by Southern transfer of products, hybridis ation with internal oligoprobes for the MBR/JH and MCR/JH bcl-2 rearrangeme nts and IHC analysis of Bcl-2 expression, were performed. PCR analysis was positive in 34.8% of patients. Bcl-2/IgH gene rearrangements were observed in 8 (34%) cases and 7 (30%) showed Bcl-2 expression on large noncleaved B- cells (centroblasts). All patients from Group A showed IHC positive reactio n on FCL remnant (small cleaved cells) but only 2 (18%) were positive in DL BCL areas, suggesting either the loss of the bcl-2 expression on the transf ormed lymphoma, or, alternatively, the development of a second disease when the first lymphoma transforms. Group B patients showed a clear correlation between PCR and IHC studies. Our results suggest a similar frequency of t( 14; 18) in DLBCLs to that reported in Europe and USA series. The discordanc e observed between PCR and IHC, particularly in Group A, points out the nec essity to perform both studies in order to detect bcl-2 gene involvement in DLBCLs.