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The future of vitamin D analogs

The active form of vitamin D(3), 1,25-dihydroxyvitamin D(3), is a major regulator of bone and calcium homeostasis. In addition, this hormone also inhibits the proliferation and stimulates the differentiation of normal as well as malignant cells. Supraphysiological doses of 1,25-dihydroxyvitamin D(3)...

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Autores principales: Leyssens, Carlien, Verlinden, Lieve, Verstuyf, Annemieke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982071/
https://www.ncbi.nlm.nih.gov/pubmed/24772087
http://dx.doi.org/10.3389/fphys.2014.00122
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author Leyssens, Carlien
Verlinden, Lieve
Verstuyf, Annemieke
author_facet Leyssens, Carlien
Verlinden, Lieve
Verstuyf, Annemieke
author_sort Leyssens, Carlien
collection PubMed
description The active form of vitamin D(3), 1,25-dihydroxyvitamin D(3), is a major regulator of bone and calcium homeostasis. In addition, this hormone also inhibits the proliferation and stimulates the differentiation of normal as well as malignant cells. Supraphysiological doses of 1,25-dihydroxyvitamin D(3) are required to reduce cancer cell proliferation. However, these doses will lead in vivo to calcemic side effects such as hypercalcemia and hypercalciuria. During the last 25 years, many structural analogs of 1,25-dihydroxyvitamin D(3) have been synthesized by the introduction of chemical modifications in the A-ring, central CD-ring region or side chain of 1,25-dihydroxyvitamin D(3) in the hope to find molecules with a clear dissociation between the beneficial antiproliferative effects and adverse calcemic side effects. One example of such an analog with a good dissociation ratio is calcipotriol (Daivonex®), which is clinically used to treat the hyperproliferative skin disease psoriasis. Other vitamin D analogs were clinically approved for the treatment of osteoporosis or secondary hyperparathyroidism. No vitamin D analog is currently used in the clinic for the treatment of cancer although several analogs have been shown to be potent drugs in animal models of cancer. Transcriptomics studies as well as in vitro cell biological experiments unraveled basic mechanisms involved in the antineoplastic effects of vitamin D and its analogs. 1,25-dihydroxyvitamin D(3) and analogs act in a cell type- and tissue-specific manner. Moreover, a blockade in the transition of the G0/1 toward S phase of the cell cycle, induction of apoptosis, inhibition of migration and invasion of tumor cells together with effects on angiogenesis and inflammation have been implicated in the pleiotropic effects of 1,25-dihydroxyvitamin D(3) and its analogs. In this review we will give an overview of the action of vitamin D analogs in tumor cells and look forward how these compounds could be introduced in the clinical practice.
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spelling pubmed-39820712014-04-25 The future of vitamin D analogs Leyssens, Carlien Verlinden, Lieve Verstuyf, Annemieke Front Physiol Physiology The active form of vitamin D(3), 1,25-dihydroxyvitamin D(3), is a major regulator of bone and calcium homeostasis. In addition, this hormone also inhibits the proliferation and stimulates the differentiation of normal as well as malignant cells. Supraphysiological doses of 1,25-dihydroxyvitamin D(3) are required to reduce cancer cell proliferation. However, these doses will lead in vivo to calcemic side effects such as hypercalcemia and hypercalciuria. During the last 25 years, many structural analogs of 1,25-dihydroxyvitamin D(3) have been synthesized by the introduction of chemical modifications in the A-ring, central CD-ring region or side chain of 1,25-dihydroxyvitamin D(3) in the hope to find molecules with a clear dissociation between the beneficial antiproliferative effects and adverse calcemic side effects. One example of such an analog with a good dissociation ratio is calcipotriol (Daivonex®), which is clinically used to treat the hyperproliferative skin disease psoriasis. Other vitamin D analogs were clinically approved for the treatment of osteoporosis or secondary hyperparathyroidism. No vitamin D analog is currently used in the clinic for the treatment of cancer although several analogs have been shown to be potent drugs in animal models of cancer. Transcriptomics studies as well as in vitro cell biological experiments unraveled basic mechanisms involved in the antineoplastic effects of vitamin D and its analogs. 1,25-dihydroxyvitamin D(3) and analogs act in a cell type- and tissue-specific manner. Moreover, a blockade in the transition of the G0/1 toward S phase of the cell cycle, induction of apoptosis, inhibition of migration and invasion of tumor cells together with effects on angiogenesis and inflammation have been implicated in the pleiotropic effects of 1,25-dihydroxyvitamin D(3) and its analogs. In this review we will give an overview of the action of vitamin D analogs in tumor cells and look forward how these compounds could be introduced in the clinical practice. Frontiers Media S.A. 2014-04-03 /pmc/articles/PMC3982071/ /pubmed/24772087 http://dx.doi.org/10.3389/fphys.2014.00122 Text en Copyright © 2014 Leyssens, Verlinden and Verstuyf. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Leyssens, Carlien
Verlinden, Lieve
Verstuyf, Annemieke
The future of vitamin D analogs
title The future of vitamin D analogs
title_full The future of vitamin D analogs
title_fullStr The future of vitamin D analogs
title_full_unstemmed The future of vitamin D analogs
title_short The future of vitamin D analogs
title_sort future of vitamin d analogs
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982071/
https://www.ncbi.nlm.nih.gov/pubmed/24772087
http://dx.doi.org/10.3389/fphys.2014.00122
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