Department of Pathology, University of Illinois at Chicago (UIC), Chicago, Illinois, USA.
Division of Urology, Department of Surgery, University of Arizona College of Medicine, Tucson, Arizona, USA.
JCI Insight. 2017 Jan 26;2(2):e91054. doi: 10.1172/jci.insight.91054.
African American (AA) men are disproportionately affected by both prostate cancer (PCa) and vitamin D deficiency compared with European American (EA) men. Vitamin D deficiency is linked to increased PCa aggressiveness and mortality. Therefore, it has been hypothesized that vitamin D deficiency may contribute to the PCa disparity between AA and EA men. We studied a cross sectional group of 60 PCa patients (AA, = 31; EA, = 29) who underwent radical prostatectomy. Vitamin D metabolites 25-hydroxyvitamin D (25(OH)D) and 1,25-dihydroxyvitamin D (1,25(OH)D) were measured in the serum and tissue by uHPLC-MS-MS. Tissue was laser capture microdissected, and gene expression was quantified by microarray. DNA isolated from whole blood was genotyped for West African ancestry markers and vitamin D-related SNPs. Serum concentrations of 25(OH)D were lower in AAs, but concentrations of 1,25(OH)D in the prostate tissue were higher compared with EAs. Expression of the vitamin D receptor was higher in prostate tissue from AAs. Expression of the extracellular receptor of vitamin D binding protein, , was positively associated with West African ancestry and inversely associated with tissue 25(OH)D concentrations in AAs. The relationships between vitamin D binding protein and vitamin D metabolites suggest that the prohormone is actively transported into the prostate, followed by intraprostatic conversion to the active hormone, rather than passive diffusion. These findings support the presence of a compensatory response in prostate tissue to vitamin D deficiency in AAs and reveal a previously unknown complexity involving tissue distribution of vitamin D metabolites. Department of Defense Prostate Cancer Research Program Idea Award for Disparities Research PC121923 (LN and RK) and the NIH 1R01MD007105 (RK).
非裔美国男性(AA)患前列腺癌(PCa)和维生素 D 缺乏症的比例明显高于欧洲裔美国男性(EA)。维生素 D 缺乏与 PCa 侵袭性和死亡率增加有关。因此,有人假设维生素 D 缺乏可能导致 AA 和 EA 男性之间的 PCa 差异。
我们研究了一组 60 名接受根治性前列腺切除术的 PCa 患者(AA,n=31;EA,n=29)的横断面研究。通过 uHPLC-MS-MS 法在血清和组织中测量维生素 D 代谢物 25-羟维生素 D(25(OH)D)和 1,25-二羟维生素 D(1,25(OH)D)。使用激光捕获显微切割技术对组织进行微解剖,并用微阵列定量基因表达。从全血中提取 DNA,用于检测西非祖源标记物和维生素 D 相关 SNP 的基因型。
AA 患者血清 25(OH)D 浓度较低,但前列腺组织中 1,25(OH)D 浓度较高。AA 患者前列腺组织中维生素 D 受体表达较高。维生素 D 结合蛋白的细胞外受体的表达与西非祖源呈正相关,与 AA 患者组织 25(OH)D 浓度呈负相关。
维生素 D 结合蛋白与维生素 D 代谢物之间的关系表明,该前激素被主动转运到前列腺中,然后在前列腺内转化为活性激素,而不是被动扩散。这些发现支持 AA 中前列腺组织存在维生素 D 缺乏的代偿反应,并揭示了一种以前未知的涉及维生素 D 代谢物组织分布的复杂性。
美国国防部前列腺癌研究计划差异研究 Idea 奖 PC121923(LN 和 RK)和 NIH 1R01MD007105(RK)。