Expression of the BCR-ABL chimeric gene in chronic myeloid leukemia re
sults in the inhibition of apoptosis, a genetically programmed process
of autonomous cell death. BCR-ABL and other genetic factors that supp
ress apoptosis confer cross-resistance to cytotoxic agents with divers
e mechanisms of action. Eradication of the chronic myeloid leukemia cl
one requires strategies that circumvent this inherent resistance to cy
totoxic therapy. We have determined that BCR-ABL expression augments t
he sensitivity of hematopoietic cells to growth factor-mediated signal
s of differentiation; hematopoietic growth factors induce the selectiv
e terminal differentiation of chronic myeloid leukemia progenitors at
concentrations that allow optimal growth of normal progenitors. Hemato
poietic growth factors may be an effective strategy for the eliminatio
n of cytotoxic therapy-resistant Leukemic cells by inducing their term
inal differentiation while allowing concomitant expansion of coexisten
t normal hematopoietic progenitors.