Cellular and Molecular mechanisms of ATRA inhibition of osteoblast-induced MDS development

ABSTRACT Osteoblasts are critical components of the hematopoietic stem cell (HSC) niche that regulate hematopoiesis. More recently, they have emerged as critical regulators of the development of hematological myeloid malignancies. We showed that a single activating mutation in -catenin signaling in osteoblasts is

sufficient to lead to the development of MDS, eventuall progressing to AML in mice. The disease is transplantable and characterized by clonal evolution at the cytogenetic level. Activated -catenin signaling is present in osteoblasts of 38% of MDS patients suggesting that this pathway may sustain dysplastic

hematopoiesis and progression to MDS and AML in humans. Our initial observations support this indication and further suggest a novel means for treating this particular population of patients. In search of a potential FDA-approved compound with the ability to inhibit -catenin signaling we came across all-trans-retinoic acid

(ATRA). ATRA is used in the treatment of acute promyelocytic leukemia where its mechanism of action relies on its ability to dissociate the NCOR-HDACL complex from RAR and allow DNA transcription and differentiation of the immature leukemic promyelocytes into mature granulocytes. However, reports from in vitro

studies indicate that ATRA has another function: it inhibits -catenin functions. We have found that inhibition of -catenin signaling in 14 MDS/ patients with active -catenin in their osteoblasts with ATRA improved their hematologic phenotype, stabilized disease status and inhibited -catenin activity. It also treated MDS and

prevented disease transformation in MDS mice expressing constitutive active -catenin in osteoblasts. Based on these observations, we hypothesize that interrupting -catenin signaling in osteoblasts of MDS mouse models and MDS patients with active -catenin in their osteoblasts by pharmacological means will

improve disease outcome. This may be achieved with ATRA, which may find a new use specifically in the treatment of the portion of MDS patients with activated -catenin in their osteoblasts. To test this hypothesis we will examine whether ATRA inhibits -catenin-induced MDS in mouse models of activated -catenin in

osteoblasts; and whether this inhibition is independent of actions on HSCs. We will also dissect the molecular mechanism of -catenin inhibition by ATRA; and, verify the significance and specificity of ATRA inhibition in cytogenetically different types of human MDS with activated -catenin in osteoblasts in vitro and in xenograft

models we developed to examine interactions between human MDS and stromal cells.