Published in:
01-02-2012 | SHORT REPORT
Anti-leukemic activity of Dasatinib in both p53wild-type and p53mutated B malignant cells
Authors:
Raffaella Bosco, Marco Rabusin, Rebecca Voltan, Claudio Celeghini, Federica Corallini, Silvano Capitani, Paola Secchiero
Published in:
Investigational New Drugs
|
Issue 1/2012
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Summary
The multi-kinase inhibitor Dasatinib induced a variable but significant decrease of viability in both p53wild-type (EHEB, JVM-2, JVM-3) and p53mutated (MEC-1, MEC-2, BJAB) prolymphocytic B leukemic cells, due to a combination of cell cycle block in G1 and apoptosis. Antibody phospho-kinase array analysis revealed that Dasatinib inhibited the phosphorylation of various kinases, including ERK1/2 and p38/MAPK as well as of STAT3 transcription factors, in both p53wild-type and p53mutated cells. Therefore, Dasatinib might offer a novel therapeutic strategy not only for p53wild-type, but also for p53mutated B malignancies that have the worst prognosis and urgently need innovative therapeutic approaches.