Belorusova Anna Y, Suh Nanjoo, Lee Hong Jin, So Jae Young, Maehr Hubert, Rochel Natacha
Department of Integrated Structural Biology, IGBMC (Institute of Genetics and of Molecular and Cellular Biology), 1 rue Laurent Fries, Illkirch, France; Centre National de la Recherche Scientifique (CNRS) UMR 7104, Illkirch, France; Institut National de la Santé et de la Recherche Médicale (INSERM) U964, Illkirch, France; Université de Strasbourg, Strasbourg, France.
Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA; Rutgers Cancer Institute of New Jersey, New Brunswick, NJ 08903, USA.
J Steroid Biochem Mol Biol. 2017 Oct;173:69-74. doi: 10.1016/j.jsbmb.2016.09.015. Epub 2016 Sep 17.
Gemini analogs of calcitriol, characterized by the extension of the C21-methyl group of calcitriol with a second chain, act as agonists of the vitamin D receptor (VDR). This second side chain of gemini is accommodated in a new cavity inside the VDR created by the structural rearrangement of the protein core. The resulting conformational change preserves the active state of the receptor and bestows gemini compounds with biological activities that exceed those of calcitriol. Of particular interest are gemini's anti-cancer properties, and in this study we demonstrate anti-proliferative and tumor-reducing abilities of BXL0124 and BXL0097, differing only by the presence or absence, respectively, of the methylene group on the A ring. BXL0124 acts as a more potent VDR agonist than its 19-nor counterpart by activating VDR-mediated transcription at lower concentrations. In a similar manner, BXL0124 is more active than BXL0097 in growth inhibition of breast cancer cells and reduction of tumor volume. Structural comparisons of BXL0097 and BXL0124, as their VDR complexes, explain the elevated activity of the latter.
骨化三醇的 Gemini 类似物,其特征在于骨化三醇的 C21 - 甲基基团通过第二条链进行延伸,可作为维生素 D 受体(VDR)的激动剂。Gemini 的这条第二条侧链容纳在由蛋白质核心结构重排形成的 VDR 内部的一个新腔中。由此产生的构象变化保持了受体的活性状态,并赋予 Gemini 化合物超过骨化三醇的生物活性。特别值得关注的是 Gemini 的抗癌特性,在本研究中,我们证明了 BXL0124 和 BXL0097 的抗增殖和肿瘤缩小能力,它们的区别仅在于 A 环上分别有无亚甲基。BXL0124 通过在较低浓度下激活 VDR 介导的转录,比其 19 - 去甲类似物更有效地作为 VDR 激动剂。以类似的方式,BXL0124 在抑制乳腺癌细胞生长和减小肿瘤体积方面比 BXL0097 更具活性。BXL0097 和 BXL0124 作为它们的 VDR 复合物的结构比较,解释了后者活性的提高。