Abstract
The bcr-abl oncogene, present in 95% of patients with chronic myelogenous leukemia (CML), has been implicated as the cause of this disease. A compound, designed to inhibit the Abl protein tyrosine kinase, was evaluated for its effects on cells containing the Bcr-Abl fusion protein. Cellular proliferation and tumor formation by Bcr-Abl-expressing cells were specifically inhibited by this compound. In colony-forming assays of peripheral blood or bone marrow from patients with CML, there was a 92-98% decrease in the number of bcr-abl colonies formed but no inhibition of normal colony formation. This compound may be useful in the treatment of bcr-abl-positive leukemias.
Original language | English (US) |
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Pages (from-to) | 561-566 |
Number of pages | 6 |
Journal | Nature medicine |
Volume | 2 |
Issue number | 5 |
DOIs | |
State | Published - 1996 |
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)