C. Ludescher et al., LOW-FREQUENCY OF ACTIVITY OF P-GLYCOPROTEIN (P-170) IN ACUTE LYMPHOBLASTIC-LEUKEMIA COMPARED TO ACUTE MYELOID-LEUKEMIA, Leukemia, 9(2), 1995, pp. 350-356
The purpose of our investigations was to measure P-glycoprotein (P-170
) activity in blast cells of 35 adults with acute myeloid leukemia (AM
L), and 24 children and adults with acute lymphoblastic leukemia (ALL)
at time of diagnosis. Studies were based on a flow cytometric assay t
hat detects efflux of the fluorescent dye rhodamine 123 (Rh123), which
is transported from the cell by the P-170 pump. Dual-fluorescence sta
ining with Rh123 and phycoerythrin-labeled monoclonal antibodies allow
ed selective measurement of Rh123 efflux in blast cells. Samples were
scored positive when the fraction of blast cells showing Rh123 efflux
exceeded 10% after 120-min incubation. Activity of P-170 was observed
in 19 (54%) of the 35 AML cases and was completely blocked in the pres
ence of multidrug resistance inhibitors. Efflux activity was significa
ntly higher in CD34-positive AML samples (p < 0.02). All AML patients
with the FAB-subtype M5 (n = 5) lacked Rh123 pumping activity (p < 0.0
3). The complete remission rate in response to induction chemotherapy
was significantly higher for Rh123-negative (11/13, 85%) than for Rh 1
23-positive AML patients (4/15, 27%) (p < 0.007). At a median follow-u
p of 9 months overall survival was significantly shorter for Rh123-pos
itive than for Rh123-negative patients (p < 0.05). In contrast to AML,
we could detect Rh123 efflux in only two (8%) out of 24 ALL cases. Th
e immunological subtypes of these two positive cases was of B-ALL and
pre-T-ALL. Bone marrow cryostat sections from 13 AML and five ALL pati
ents were further analyzed for staining with monoclonal antibodies MM4
.17 and JSB1. Ten of 13 AML and two of five ALL cases expressed the MD
R protein. Our results indicate that there is a rather low frequency o
f P-170 pumping activity in ALL compared with AML. Further, functional
activity of P-170 contributes to chemoresistance in de novo AML.