RT Journal Article
SR Electronic
T1 PKC Potentiates Tyrosine Kinase Inhibitors STI571 and Dasatinib Cytotoxic Effect
JF Anticancer Research
JO Anticancer Res
FD International Institute of Anticancer Research
SP 3347
OP 3356
VO 34
IS 7
A1 ARACELI TOBÍO
A1 AMPARO ALFONSO
A1 LUIS M. BOTANA
YR 2014
UL http://ar.iiarjournals.org/content/34/7/3347.abstract
AB Aim: The aim of the present study was to determine the relationship between the tyrosine kinase inhibitors, STI571 and dasatinib effects and protein kinase C (PKC) status in HMC-1560 and HMC-1560,816 cell lines. Material and Methods: Viability results were obtained by two different methods: MTT and a flow cytometry with Annexin V-FITC/PI double-staining protocol. The lipid-based transfection method was used to silence PKC. Results: Long-term PKC activation induces apoptosis in both HMC-1 cell lines. Moreover, PKC activation potentiates STI571 and dasatinib cytotoxic effects in HMC-1560 and HMC-1560,816 cells, respectively, by increasing necrotic populations. To investigate this PKC effect, the role of PKCδ, an isoform intimately related with apoptotic cell death, was studied. The results obtained evidence that either STI571 or dasatinib apoptotic cell death are PKCδ-dependent. Particularly, STI571 showed less dependence to PKCδ than dasatinib. Conclusion: PKCδ modulation is essential and determines mastocytosis treatment effectiveness, since STI571 and dasatinib effects are PKCδ-dependent.