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Review

Promise of vitamin D analogues in the treatment of hyperproliferative conditions

Department of Biochemistry, Queen's University, Kingston, Ontario, Canada

Requests for reprints: Glenville Jones, Department of Biochemistry, Queen's University, Kingston, Ontario, Canada K7L 3N6. Phone: 613-533-2494; Fax: 613-533-2022. E-mail: gj1{at}post.queensu.ca

1,25-Dihydroxyvitamin D₃ [1,25-(OH)₂D₃; calcitriol] is best known as a hormone involved in calcium homeostasis but is also a potent antiproliferative agent in many cell types, particularly epithelial cells. 1,25(OH)₂D₃ mediates its actions through a classic steroid hormone-like transcriptional mechanism by influencing the expression of hundreds of genes. Effects of 1,25(OH)₂D₃ have been observed on expression of cell cycle regulators, growth factors and their receptors, apoptotic machinery, metastatic potential, and angiogenesis; all of which have some effect on hyperproliferative conditions. This minireview focuses on the anticancer potential of 1,25(OH)₂D₃ and its analogues by summarizing the promising data from animal and human trials of 1,25(OH)₂D₃ and some of the more interesting synthetic vitamin D analogues in the treatment of a variety of different animal cancer models and in human patients with advanced cancer. Optimal administration of vitamin D analogues is only just being achieved with high-dose intermittent administration overcoming bioavailability and hypercalcemia problems and combination therapy with cytotoxic agents (taxols and cisplatins), antiresorptive agents (bisphosphonates), or cytochrome P450 inhibitors being attempted. Although the potential of vitamin D as an antiproliferative drug has been realized in the treatment of psoriasis and in parathyroid cell hyperplasia associated with secondary hyperparathyroidism, the search for an anticancer treatment incorporating a vitamin D analogue remains elusive. [Mol Cancer Ther 2006;5(4):797–808]

Received 12/27/05; revised 1/31/06; accepted 2/16/06.

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