PT  - JOURNAL ARTICLE
AU  - Zhang, Zhihong
AU  - Meier, Kathryn E.
TI  - New Assignments for Multitasking Signal Transduction Inhibitors
AID  - 10.1124/mol.106.023721
DP  - 2006 May 01
TA  - Molecular Pharmacology
PG  - 1510--1512
VI  - 69
IP  - 5
4099  - http://molpharm.aspetjournals.org/content/69/5/1510.short
4100  - http://molpharm.aspetjournals.org/content/69/5/1510.full
SO  - Mol Pharmacol2006 May 01; 69
AB  - An article presented in this issue of Molecular Pharmacology (p. 1527) provides an intriguing example of how tyrosine kinase inhibitors can be put to many uses. In this article, the action of dasatinib (BMS-354825) is contrasted with that of imatinib, a kinase inhibitor that is currently being used to treat chronic myelogenous leukemia and other disorders. Both pharmacologic inhibitors target several tyrosine kinases, including Bcr-Abl and the platelet-derived growth factor receptor (PDGFR). Up to this point, the PDGFR has not been a primary therapeutic target for this class of agents. The work of Chen and colleagues shows that dasatinib is a particularly potent inhibitor of PDGFR and that the compound also targets Src kinase. The authors suggest that this combination of activities could be useful in the treatment of vascular obstructive diseases. Although a lack of absolute specificity has typically been regarded as a pharmacologic drawback, this study exemplifies how drugs with multiple molecular targets can potentially provide a very beneficial spectrum of therapeutic activities in multiple disease states.