摘要 |
The present invention pertains to methods of reducing the activity of a mutant KIT protein and also to methods of reducing the concentration of a mutant KIT protein. The mutant KIT protein can be in a cell, or the mutant KIT protein can be in a host. The present inventive methods comprise administering to the cell or the host either an inhibitor of Hsp90, which binds to an ATP binding domain of Hsp90, or a compound comprising a macrocycle, such as 17-allylamino-17-demethoxygeldanamycin. The mutant KIT protein can comprise a mutation in the kinase domain or the juxtamembrane domain. The host can be afflicted with a disease that is characterized by a mutant KIT protein, such as mastocytosis, gastrointestinal stromal tumor, mast cell leukemia, myelogenous leukemia, lymphoma, and testicular cancer. |
申请人 |
THE GOVERNMENT OF THE UNITED STATES OF AMERICA, REPRESENTED BY THE SECRETARY, DEPT. OF HEALTH AND HUMAN SERVICES;FUMO, GERARD;NECKERS, LEN |
发明人 |
FUMO, GERARD;NECKERS, LEN |