E2F-1 is a transcription factor that mediates cell cycle progression f
rom the G(1) to S phase and is normally regulated by a group of protei
ns, including cyclin D1, Although deregulation of E2F-1 is implicated
in neoplastic transformation, in situ examination of this protein has
not been performed to date. Using an immunohistochemical technique app
lied to routinely fixed, paraffin-embedded tissue sections, we evaluat
ed E2F-1 expression in reactive lymphoid tissues and in 124 cases of n
on-Hodgkin's lymphoma (NHL) of various types. In reactive lymphoid tis
sues, E2F-1 was expressed predominantly by large noncleaved cells in g
erminal centers and by a small subset of cortical thymocytes. Mantle z
ones and splenic marginal zones were negative. Among the NHLs, four ty
pes had a relatively high percentage (> 20%) of E2F-1-positive cells:
mantle cell lymphoma (19 of 19), lymphoblastic lymphoma (5 of 5), smal
l noncleaved cell lymphoma (4 of 6), and hepatosplenic gamma delta T-c
ell lymphoma (3 of 3). The consistent detection of many E2F-1-positive
cells in mantle cell lymphoma is in contrast to other small B-cell NH
Ls (n = 29), which had relatively few (< 10%) E2F-1-positive cells. Th
is finding suggests that immunohistochemical staining for E2F-1 as a s
upplement to the existing markers, such as cyclin D1, might be useful
in the differential diagnosis of NHLs composed of small B cells.