| Literature DB >> 18401419 |
A L Feldman1, D X Sun, M E Law, A J Novak, A D Attygalle, E C Thorland, S R Fink, J A Vrana, B L Caron, W G Morice, E D Remstein, K L Grogg, P J Kurtin, W R Macon, A Dogan.
Abstract
Peripheral T-cell lymphomas (PTCLs) are fatal in the majority of patients and novel treatments, such as protein tyrosine kinase (PTK) inhibition, are needed. The recent finding of SYK/ITK translocations in rare PTCLs led us to examine the expression of Syk PTK in 141 PTCLs. Syk was positive by immunohistochemistry (IHC) in 133 PTCLs (94%), whereas normal T cells were negative. Western blot on frozen tissue (n=6) and flow cytometry on cell suspensions (n=4) correlated with IHC results in paraffin. Additionally, western blot demonstrated that Syk-positive PTCLs show tyrosine (525/526) phosphorylation, known to be required for Syk activation. Fluorescence in situ hybridization showed no SYK/ITK translocation in 86 cases. Overexpression of Syk, phosphorylation of its Y525/526 residues and the availability of orally available Syk inhibitors suggest that Syk merits further evaluation as a candidate target for pharmacologic PTK inhibition in patients with PTCL.Entities:
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Year: 2008 PMID: 18401419 PMCID: PMC2778211 DOI: 10.1038/leu.2008.77
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528