Department of Biological Sciences, Hockmeyer Hall of Structural Biology, Purdue University, West Lafayette, IN, USA.
IUBMB Life. 2013 Sep;65(9):787-92. doi: 10.1002/iub.1199. Epub 2013 Aug 5.
Calcitriol, the biologically active form of vitamin D, is known to function as an important anticancer agent. The exact mechanism by which calcitriol exerts its effects remains unknown. Recent evidence suggests a link between calcitriol-induced, free-radical-mediated DNA damage and cell death, in the presence of elevated levels of copper, such as those observed in malignant cells. As calcitriol is a lipid-soluble molecule, its interaction with DNA and copper would require a "chaperone"-like molecule, which binds the relatively hydrophobic calcitriol and polar DNA. A candidate protein is the vitamin D receptor (VDR), which binds both molecules. Using the recently elucidated full-length structure of the VDR molecule, we present and discuss three possible mechanisms to explain the interaction between calcitriol and DNA, as mediated by VDR.
骨化三醇,维生素 D 的生物活性形式,已知具有重要的抗癌作用。骨化三醇发挥作用的确切机制尚不清楚。最近的证据表明,在铜水平升高的情况下,如在恶性细胞中观察到的那样,骨化三醇诱导的自由基介导的 DNA 损伤和细胞死亡之间存在联系。由于骨化三醇是一种脂溶性分子,因此它与 DNA 和铜的相互作用需要一种“伴侣”样分子,该分子结合相对疏水性的骨化三醇和极性 DNA。候选蛋白是维生素 D 受体 (VDR),它结合这两种分子。利用最近阐明的全长 VDR 分子结构,我们提出并讨论了三种可能的机制来解释 VDR 介导的骨化三醇与 DNA 之间的相互作用。