RT Journal Article
SR Electronic
T1 The Appearance of Drug Resistance
JF Science's STKE
JO Sci. STKE
FD American Association for the Advancement of Science
SP tw15
OP tw15
DO 10.1126/stke.2001.94.tw15
VO 2001
IS 94
YR 2001
UL http://stke.sciencemag.org/content/2001/94/tw15.abstract
AB STI-571 is a new cancer drug that has shown remarkable efficacy in patients who are in the early stages of chronic myeloid leukemia (CML). The drug inhibits the Abl kinase, which is constitutively activated in CML patients, because they carry a characteristic chromosomal translocation that fuses the ABL gene with the unrelated BCR gene. Patients in whom CML has progressed to a stage called blast crisis respond to STI-571 initially, but then develop resistance. Gorre et al. studied nine patients who had relapsed after STI-571 treatment and found that all nine showed reactivation of the Bcr-Abl signaling pathway. Six patients had acquired the same amino acid substitution in the Abl kinase domain--a change predicted to alter interaction of the kinase with the drug--and the other three showed BCR-ABL gene amplification. Identification of the mechanisms responsible for STI-571 resistance may facilitate the design of next-generation drugs for CML. (See the 22 June news story by Marx.) M. E. Gorre, M. Mohammed, K. Ellwood, N. Hsu, R. Paquette, P. N. Rao, C. L. Sawyers, Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification. Science 293, 876-880 (2001). [Abstract] [Full Text] J. Marx, Why some leukemia cells resist STI-571. Science 292, 2231-2233 (2001). [Full Text]