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P53 Activation of Mesenchymal Stromal Cells Partially Abrogates Microenvironment-mediated Resistance to FLT3 Inhibition in AML Through HIF-1α-mediated Down-regulation of CXCL12

Overview
Journal Blood
Publisher Elsevier
Specialty Hematology
Date 2011 Aug 27
PMID 21868571
Citations 61
Authors
Affiliations
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Abstract

Fms-like tyrosine kinase-3 (FLT3) inhibitors have been used to overcome the dismal prognosis of acute myeloid leukemia (AML) with FLT3 mutations. Clinical results with FLT3 inhibitor monotherapy have shown that bone marrow responses are commonly less pronounced than peripheral blood responses. We investigated the role of p53 in bone marrow stromal cells in stromal cell-mediated resistance to FLT3 inhibition in FLT3 mutant AML. While the FLT3 inhibitor FI-700 induced apoptosis in FLT3 mutant AML cells, apoptosis induction was diminished under stromal coculture conditions. Protection appeared to be mediated, in part, by CXCL12 (SDF-1)/CXCR4 signaling. The protective effect of stromal cells was significantly reduced by pre-exposure to the HDM2 inhibitor Nutlin-3a. p53 activation by Nutlin-3a was not cytotoxic to stromal cells, but reduced CXCL12 mRNA levels and secretion of CXCL12 partially through p53-mediated HIF-1α down-regulation. Results show that p53 activation in stroma cells blunts stroma cell-mediated resistance to FLT3 inhibition, in part through down-regulation of CXCL12. This is the first report of Nutlin effect on the bone marrow environment. We suggest that combinations of HDM2 antagonists and FLT3 inhibitors may be effective in clinical trials targeting mutant FLT3 leukemias.

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References
1.
Ceradini D, Kulkarni A, Callaghan M, Tepper O, Bastidas N, Kleinman M . Progenitor cell trafficking is regulated by hypoxic gradients through HIF-1 induction of SDF-1. Nat Med. 2004; 10(8):858-64. DOI: 10.1038/nm1075. View

2.
Whitman S, Ruppert A, Radmacher M, Mrozek K, Paschka P, Langer C . FLT3 D835/I836 mutations are associated with poor disease-free survival and a distinct gene-expression signature among younger adults with de novo cytogenetically normal acute myeloid leukemia lacking FLT3 internal tandem duplications. Blood. 2007; 111(3):1552-9. PMC: 2214747. DOI: 10.1182/blood-2007-08-107946. View

3.
Sato T, Yang X, Knapper S, White P, Smith B, Galkin S . FLT3 ligand impedes the efficacy of FLT3 inhibitors in vitro and in vivo. Blood. 2011; 117(12):3286-93. PMC: 3069670. DOI: 10.1182/blood-2010-01-266742. View

4.
Fukuda S, Broxmeyer H, Pelus L . Flt3 ligand and the Flt3 receptor regulate hematopoietic cell migration by modulating the SDF-1alpha(CXCL12)/CXCR4 axis. Blood. 2004; 105(8):3117-26. DOI: 10.1182/blood-2004-04-1440. View

5.
Moskovits N, Kalinkovich A, Bar J, Lapidot T, Oren M . p53 Attenuates cancer cell migration and invasion through repression of SDF-1/CXCL12 expression in stromal fibroblasts. Cancer Res. 2006; 66(22):10671-6. DOI: 10.1158/0008-5472.CAN-06-2323. View