Nitric Oxide Suppresses Tumor Cell Migration through N-Myc Downstream-regulated Gene-1 (NDRG1) Expression ROLE OF CHELATABLE IRON

N-Myc downstream-regulated gene 1 (NDRG1) is a ubiquitous cellular protein that is up-regulated under a multitude of stress and growth-regulatory conditions. Although the exact cellular functions of this protein have not been elucidated, mutations in this gene or aberrant expression of this protein have been linked to both tumor suppressive and oncogenic phenotypes. Previous reports have demonstrated that NDRG1 is strongly up-regulated by chemical iron chelators and hypoxia, yet its regulation by the free radical nitric oxide ((NO)-N-center dot) has never been demonstrated. Herein, we examine the chemical biology that confers NDRG1 responsiveness at the mRNA and protein levels to (NO)-N-center dot. We demonstrate that the interaction of (NO)-N-center dot with the chelatable iron pool (CIP) and the appearance of dinitrosyliron complexes (DNIC) are key determinants. Using HCC 1806 triple negative breast cancer cells, we find that NDRG1 is up-regulated by physiological (NO)-N-center dot concentrations in a dose- and time-dependant manner. Tumor cell migration was suppressed by NDRG1 expression and we excluded the involvement of HIF-1 alpha, sGC, N-Myc, and c-Myc as upstream regulatory targets of (NO)-N-center dot. Augmenting the chelatable iron pool abolished (NO)-N-center dot-mediated NDRG1 expression and the associated phenotypic effects. These data, in summary, reveal a link between (NO)-N-center dot, chelatable iron, and regulation of NDRG1 expression and signaling in tumor cells.