Prevention of renal cell carcinoma by active vitamin D-3

We studied the serum levels of 1,25-dihydroxyvitamin I) [1,25(OH)(2)D (Vit D)] in patients with renal cell carcinoma (RCC) and the influence of 1,25(O H)(2) D-3 (Vit D-3) on gap junctional intercellular communication (GJIC) du ring carcinogenesis. The serum Vit D levels were measured by a competitive protein-binding assay using the chromatographic method. Using the [3-(4,5-d imethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] (MIT) assay, noncytot oxic concentrations of Vit D-3 and the tumor promoters N-nitrosodimethylami ne (NDMA) and N-ethyl-N-hydroxyethylnitrosamine (EHEN) were tested against cultured human renal proximal tubular cells (HRPTCs). GJIC function was ass ayed by the scrape-loading dye transfer technique. Cx43 mRNA expression was also examined by the reverse transcriptase-polymerase chain reaction (RT-P CR). Serum Vit D levels in patients with RCC were lower than those in contr ols (p<0.001). Patients with T3 to T4 (rapid-growth) tumors had lower level s of Vit D than did patients with T1 to T2 (slow-growth) tumors (p<0.001). Vit D-3 enhanced the GJIC function of HRPTCs (p<0.05), whereas NDMA and EHE N suppressed it (p<0.05). When the cells were treated with tumor promoters and Vit D-3 simultaneously, the GJIC functions remained at pretreatment lev els. We also demonstrated Cx43 mRNA expression in RPTECs treated with EHEN and VitD(3) simultaneously. These data suggest that a decrease in the serum Vit D level is one of the risk factors for development and progression of RCC, and Vit D-3 may prevent RCC by preserving GJIC during carcinogenesis.