Pancreatic cancer cells express 25-hydroxyvitamin D-1α-hydroxylase and their proliferation is inhibited by the prohormone 25-hydroxyvitamin D3

• Published in: Carcinogenesis (New York) Vol. 25; no. 6; pp. 1015 - 1026
• Main Authors: Schwartz, Gary G., Eads, Dawn, Rao, Anuradha, Cramer, Scott D., Willingham, Mark C., Chen, Tai C., Jamieson, Daniel P., Wang, Lilin, Burnstein, Kerry L., Holick, Michael F., Koumenis, Constantinos
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 01.06.2004
• Subjects: 1α(OH)ase; 25(OH)2D3; 25(OH)2D3 receptor; 25-dihydroxyvitamin D3; 25-hydroxyvitamin-1-α-hydroxylase; Base Sequence; Biological and medical sciences; Calcifediol - pharmacology; Carcinogenesis, carcinogens and anticarcinogens; Cell Cycle - drug effects; Cell Division - drug effects; Cell Line, Tumor; Cytochrome P-450 Enzyme System - genetics; Cytochrome P-450 Enzyme System - metabolism; DNA Primers; Humans; Medical sciences; Pancreatic Neoplasms - enzymology; Pancreatic Neoplasms - pathology; PBS; phosphate-buffered saline; RNA, Messenger - genetics; RNA, Messenger - metabolism; Steroid Hydroxylases - genetics; Steroid Hydroxylases - metabolism; Tumors; VDR; VDR response element; VDRE; Vitamin D3 24-Hydroxylase; Cell proliferation; Enzyme; Hydroxylase; Pancreas cancer; Digestive diseases; Inhibitor; Oxidoreductases; Malignant tumor; Prohormone; Tumor cell; Pancreatic disease
• ISSN: 0143-3334; 1460-2180
• DOI: 10.1093/carcin/bgh086

The steroid hormone 1,25-dihydroxyvitamin D3, [1,25(OH)2D3, calcitriol], the active metabolite of vitamin D, exerts pleiotropic antitumor effects against several malignancies. However, the clinical use of this hormone is limited by hypercalcemia. 25-Hydroxyvitamin D3, the prohormone of 1,25(OH)2D3, is hydroxylated to the active hormone by the enzyme 25-hydroxyvitamin-1-α-hydroxylase [1α(OH)ase]. 1α(OH)ase is found primarily in the kidney, but also is expressed in the prostate, colon and other tissues. Using immunohistochemistry, we report that 1α(OH)ase is highly expressed in both normal and malignant pancreatic tissue. Expression of this enzyme and enzymatic activity was also detected in four pancreatic tumor cell lines. 25(OH)D3 inhibited the growth of three of four pancreatic cell lines in a manner that correlated with the level of induction of the cyclin-dependent kinase inhibitors p21 and p27 and with the induction of cell cycle arrest at the G1/S checkpoint. The growth of a cell line stably transfected with a mutant Ki-ras allele and of a second cell line with an endogenous Ki-ras activating mutation was also inhibited by 25(OH)D3, indicating that activating Ki-Ras mutations, which occur in almost 90% of pancreatic adenocarcinomas, do not interfere with the growth-inhibitory effects of 25(OH)D3. The expression of 1α(OH)ase in normal and malignant pancreatic tissue and the antiproliferative effects of the prohormone in these cells, suggest that 25(OH)D3 may offer possible therapeutic and chemopreventive options for pancreatic cancer.