Data from A Unique Pharmacophore for Activation of the Nuclear Orphan Receptor Nur77 <i>In vivo</i> and <i>In vitro</i>

Abstract

<div>Abstract<p>Nur77 is a steroid orphan receptor that plays a critical role in regulating proliferation, differentiation, and apoptosis, including acting as a switch for Bcl-2 function. We previously reported that the octaketide cytosporone B (Csn-B) is a natural agonist for Nur77. In this study, we synthesized a series of Csn-B analogues and performed a structure-activity analysis that suggested criteria for the development of a unique pharmacophore to activate Nur77. The components of the pharmacophore necessary for binding Nur77 included the benzene ring, the phenolic hydroxyl group, and the acyl chain of the Csn-B scaffold, whereas the key feature for activating the biological function of Nur77 was the ester group. Csn-B analogues that bound Nur77 tightly not only stimulated its transactivation activity but also initiated mitochondrial apoptosis by means of novel cross-talk between Nur77 and BRE, an antiapoptotic protein regulated at the transcriptional level. Notably, the derivative n-amyl 2-[3,5-dihydroxy-2-(1-nonanoyl)phenyl]acetate exhibited greater antitumor activity <i>in vivo</i> than its parent compounds, highlighting particular interest in this compound. Our findings describe a pathway for rational design of Csn-B–derived Nur77 agonists as a new class of potent and effective antitumor agents. Cancer Res; 70(9); 3628–37. ©2010 AACR.</p></div>