Background: Both the multi-kinase inhibitor Sorafenib and the small molecule inhibitor of the MDM2/p53 interaction Nutlin-3, used alone, have shown promising anti-leukemic activity in acute myeloid leukemia cells. Thus, in this study we have investigated the effect of Sorafenib plus Nutlin-3 combination in acute myeloid leukemia. Design and Methods: Primary acute myeloid leukemia blasts (n=13) and FLT3wild-type/p53wild-type (OCI-AML3), FLT3mutated/p53wild-type (MOLM), FLT3mutated/p53mutated (MV4-11), FLT3wild-type/p53deleted (HL60) or FLT3wild-type/p53mutated (NB4) acute myeloid cell lines were exposed to Sorafenib, used alone or in association with Nutlin-3 at 1:1 ratio, in a range of clinically achievable concentrations (1-10 uM). Induction of apoptosis and autophagy was evaluated by transmission electron microscopy and by specific flow cytometry analyses. The levels of Mcl-1, p53 and Bak proteins were analyzed by Western blot; knock-down of Bax and Bak gene expression was performed in transfection experiments with specific siRNA.Results: The Sorafenib+Nutlin-3 drug combination exhibits synergistic cytotoxicity in primary acute myeloid leukemia blasts and in acute myeloid leukemia cell lines with maximal cytotoxicity in FLT3mutated MV4-11 and MOLM, followed by the FLT3wild-type OCI-AML3, HL60 and NB4. The cytotoxic activity of Sorafenib+Nutlin-3 was characterized by an increase of both apoptosis and autophagy. Moreover, Bax and Bak showed a prominent role in mediating the decrease of cell viability in response to the drug combination in p53wild-type OCI-AML3 and p53deleted HL-60 cells, respectively, as demonstrated in transfection experiments performed with specific siRNA.Conclusions: Our data demonstrate that acute myeloid leukemia cells show a variable but overall good susceptibility to the innovative therapeutic combination Sorafenib+Nutlin-3, which differentially involves the pro-apoptotic Bcl-2 family members Bax and Bak in p53wild-type and p53deleted cells.
ZAULI, G., Celeghini C, MELLONI, E., VOLTAN, R., Ongari M, Tiribelli M, et al. (2012). The Sorafenib plus Nutlin-3 combination promotes synergistic cytotoxicity in acute myeloid leukemic cells irrespectively of the FLT3 and p53 status. HAEMATOLOGICA, 97(11), 1722-1730 [10.3324/haematol.2012.062083].
The Sorafenib plus Nutlin-3 combination promotes synergistic cytotoxicity in acute myeloid leukemic cells irrespectively of the FLT3 and p53 status
Celeghini C;MELLONI, Elisabetta;Lanza FValidation
;
2012
Abstract
Background: Both the multi-kinase inhibitor Sorafenib and the small molecule inhibitor of the MDM2/p53 interaction Nutlin-3, used alone, have shown promising anti-leukemic activity in acute myeloid leukemia cells. Thus, in this study we have investigated the effect of Sorafenib plus Nutlin-3 combination in acute myeloid leukemia. Design and Methods: Primary acute myeloid leukemia blasts (n=13) and FLT3wild-type/p53wild-type (OCI-AML3), FLT3mutated/p53wild-type (MOLM), FLT3mutated/p53mutated (MV4-11), FLT3wild-type/p53deleted (HL60) or FLT3wild-type/p53mutated (NB4) acute myeloid cell lines were exposed to Sorafenib, used alone or in association with Nutlin-3 at 1:1 ratio, in a range of clinically achievable concentrations (1-10 uM). Induction of apoptosis and autophagy was evaluated by transmission electron microscopy and by specific flow cytometry analyses. The levels of Mcl-1, p53 and Bak proteins were analyzed by Western blot; knock-down of Bax and Bak gene expression was performed in transfection experiments with specific siRNA.Results: The Sorafenib+Nutlin-3 drug combination exhibits synergistic cytotoxicity in primary acute myeloid leukemia blasts and in acute myeloid leukemia cell lines with maximal cytotoxicity in FLT3mutated MV4-11 and MOLM, followed by the FLT3wild-type OCI-AML3, HL60 and NB4. The cytotoxic activity of Sorafenib+Nutlin-3 was characterized by an increase of both apoptosis and autophagy. Moreover, Bax and Bak showed a prominent role in mediating the decrease of cell viability in response to the drug combination in p53wild-type OCI-AML3 and p53deleted HL-60 cells, respectively, as demonstrated in transfection experiments performed with specific siRNA.Conclusions: Our data demonstrate that acute myeloid leukemia cells show a variable but overall good susceptibility to the innovative therapeutic combination Sorafenib+Nutlin-3, which differentially involves the pro-apoptotic Bcl-2 family members Bax and Bak in p53wild-type and p53deleted cells.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
