BCL-2 EXPRESSION CORRELATES WITH LOWER PROLIFERATIVE ACTIVITY IN THE INTERMEDIATE-GRADE AND HIGH-GRADE NON-HODGKINS-LYMPHOMAS - AN EASTERN CCOOPERATIVE ONCOLOGY GROUP AND SOUTHWEST-ONCOLOGY-GROUP COOPERATIVE LABORATORY STUDY
Jn. Winter et al., BCL-2 EXPRESSION CORRELATES WITH LOWER PROLIFERATIVE ACTIVITY IN THE INTERMEDIATE-GRADE AND HIGH-GRADE NON-HODGKINS-LYMPHOMAS - AN EASTERN CCOOPERATIVE ONCOLOGY GROUP AND SOUTHWEST-ONCOLOGY-GROUP COOPERATIVE LABORATORY STUDY, Blood, 91(4), 1998, pp. 1391-1398
An inverse relationship between BCL-2 expression and cell cycle transi
tion has been suggested by recent studies in murine models. To investi
gate the clinical relevance of these laboratory studies, a group of 11
6 paraffin-embedded non-Hodgkin's lymphoma (NHL) biopsy specimens (Wor
king Formulation Groups D-H, and J) from a cooperative group study of
cellular DNA content were analyzed for the 14;18 translocation using p
olymerase chain reaction (PCR)-based methods and, if sufficient tissue
remained, for BCL-2 and BAX expression by immunohistochemistry. The r
esults of these studies were then compared with the results of the pre
viously performed flow cytometric analysis of ploidy and proliferative
activity (S-phase-fraction). BCL-2 expression was inversely associate
d with proliferative activity (P = .001; n = 41), but there was no ass
ociation between staining for Fax and %S-phase. Ploidy was not associa
ted with either BCL-2 or BAX expression. The t(14;18) was detected in
21 of the 54 cases in which PCR-amplifiable DNA was recovered; 20 of t
hese occurred at the major breakpoint region and 1 at the minor breakp
oint region. High levels of BCL-2 or BAX expression occurred independe
ntly of t(14;18). There was no association between t(14;18) and either
ploidy or proliferative activity. The inverse relationship between BC
L-2 expression and proliferative activity in the intermediate- and hig
h-grade NHLs is consistent with recent studies suggesting that Bcl-2 b
oth retards entry into the cell cycle and inhibits apoptosis. (C) 1998
by The American Society of Hematology.