Prostatic compensation of the vitamin D axis in African American men
Zachary Richards, … , Rick Kittles, Larisa Nonn
Zachary Richards, … , Rick Kittles, Larisa Nonn
Published January 26, 2017
Citation Information: JCI Insight. 2017;2(2):e91054. https://doi.org/10.1172/jci.insight.91054.
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Clinical Research and Public Health Endocrinology Oncology

Prostatic compensation of the vitamin D axis in African American men

Abstract

BACKGROUND. 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.

METHODS. We studied a cross sectional group of 60 PCa patients (AA, n = 31; EA, n = 29) who underwent radical prostatectomy. Vitamin D metabolites 25-hydroxyvitamin D (25(OH)D) and 1,25-dihydroxyvitamin D (1,25(OH)2D) 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.

RESULTS. Serum concentrations of 25(OH)D were lower in AAs, but concentrations of 1,25(OH)2D 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, LRP2, was positively associated with West African ancestry and inversely associated with tissue 25(OH)D concentrations in AAs.

CONCLUSIONS. The relationships between vitamin D binding protein LRP2 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.

FUNDING. Department of Defense Prostate Cancer Research Program Idea Award for Disparities Research PC121923 (LN and RK) and the NIH 1R01MD007105 (RK).

Authors

Zachary Richards, Ken Batai, Rachael Farhat, Ebony Shah, Andrew Makowski, Peter H. Gann, Rick Kittles, Larisa Nonn

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Figure 4

Megalin is present in prostate epithelium, and gene expression of Megalin (LRP2) correlates with ancestry and prostatic 25-hydroxyvitamin D.

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Megalin is present in prostate epithelium, and gene expression of Megali...
(A) Affymetrix array expression (reported as log2) of Megalin (LRP2) in benign epithelium collected from fresh frozen radical prostatectomy specimens by laser capture microdissection (European American [EA], n = 13; African American [AA], n = 13). Comparison of gene expression by ancestry group and correlation to percent West African ancestry for LRP2. P < 0.1; differences between ancestry determined by 2-sided Wilcoxon signed-rank test, and correlations determined by Spearman’s rank. (B) Comparison by ancestry group of correlation between LRP2 and 25(OH)D in the serum and prostate tissue. (C) Comparison by ancestry group of correlation between the vitamin D metabolites 25(OH)D (EA, n = 28; AA, n = 28) and 1,25(OH)2D (EA, n = 18; AA, n = 15) between the serum and prostate tissue. (D) Benign and cancer areas of prostate tissue from a radical prostatectomy tissue specimen immunofluorescently stained for Megalin (green) and DAPI (blue) nuclear counterstain.