Cytoprotective effect of imatinib mesylate in non-BCR-ABL-expressing cells along with autophagosome formation.

Autor: Ohtomo T; Department of Biochemistry, Tokyo Medical University, Tokyo, Japan., Miyazawa K, Naito M, Moriya S, Kuroda M, Itoh M, Tomoda A
Jazyk: angličtina
Zdroj: Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2010 Jan 01; Vol. 391 (1), pp. 310-5. Date of Electronic Publication: 2009 Nov 11.
DOI: 10.1016/j.bbrc.2009.11.055
Abstrakt: Treatment with imatinib mesylate (IM) results in an increased viable cell number of non-BCR-ABL-expressing cell lines by inhibiting spontaneous apoptosis. Electron microscopy revealed an increase of autophagosomes in response to IM. IM attenuated the cytotoxic effect of cytosine arabinoside, as well as inhibiting cell death with serum-deprived culture. Cytoprotection with autophagosome formation by IM was observed in various leukemia and cancer cell lines as well as normal murine embryonic fibroblasts (MEFs). Complete inhibition of autophagy by knockdown of atg5 in the Tet-off atg5(-/-) MEF system attenuated the cytoprotective effect of IM, indicating that the effect is partially dependent on autophagy. However, cytoprotection by IM was not mediated through suppression of ROS production via mitophagy, ER stress via ribophagy, or proapoptotic function of ABL kinase. Although the target tyrosine kinase(s) of IM remains unclear, our data provide novel therapeutic possibilities of using IM for cytoprotection.
(Copyright 2009 Elsevier Inc. All rights reserved.)
Databáze: MEDLINE
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