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Vitamin D receptor as a therapeutic target for benign prostatic hyperplasia
The bioactive form of vitamin D, 1α, 25-dihydroxyvitamin D3 (1α, 25(OH)2D3), is a secosteroid hormone that binds to the vitamin D receptor (VDR), a member of the nuclear receptor super-family expressed in many cell types, and modulates a variety of biological functions. 1α, 25(OH)2D3 is essential fo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3579114/ https://www.ncbi.nlm.nih.gov/pubmed/23450267 http://dx.doi.org/10.4103/0970-1591.105745 |
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author | Manchanda, Parmeet Kaur Kibler, Aaron J Zhang, Mei Ravi, Janani Bid, Hemant K. |
author_facet | Manchanda, Parmeet Kaur Kibler, Aaron J Zhang, Mei Ravi, Janani Bid, Hemant K. |
author_sort | Manchanda, Parmeet Kaur |
collection | PubMed |
description | The bioactive form of vitamin D, 1α, 25-dihydroxyvitamin D3 (1α, 25(OH)2D3), is a secosteroid hormone that binds to the vitamin D receptor (VDR), a member of the nuclear receptor super-family expressed in many cell types, and modulates a variety of biological functions. 1α, 25(OH)2D3 is essential for bone and mineral homeostasis, but also regulates growth and differentiation of multiple cell types, and displays immunoregulatory and anti-inflammatory activities. The antiproliferative, prodifferentiative, antibacterial, immunomodulatory and anti-inflammatory properties of synthetic VDR agonists could be exploited to treat a variety of chronic inflammatory and autoimmune diseases, including benign prostatic hyperplasia (BPH). It has been hypothesized that VDR may influence both the risk of a variety of diseases and their occurrence and prognosis. However, earlier studies investigating the associations between specific VDR polymorphisms and various diseases often show controversial results. We performed a systematic review of the current literature on vitamin D and BPH using the PubMed and Web of Knowledge databases. The aim of this review is to summarize the current knowledge on the utility of the VDR gene regarding prostate growth as well as the pathogenesis and treatment of BPH, a complex syndrome characterized by a static component related to prostate overgrowth, a dynamic component responsible for urinary storage symptoms, and an inflammatory component. Despite the massive advances in recent decades, further research is needed to fully characterize the exact underlying mechanisms of VDR action on BPH and to comprehend how these cellular changes translate into clinical development in physical concert. |
format | Online Article Text |
id | pubmed-3579114 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-35791142013-02-28 Vitamin D receptor as a therapeutic target for benign prostatic hyperplasia Manchanda, Parmeet Kaur Kibler, Aaron J Zhang, Mei Ravi, Janani Bid, Hemant K. Indian J Urol Review Article The bioactive form of vitamin D, 1α, 25-dihydroxyvitamin D3 (1α, 25(OH)2D3), is a secosteroid hormone that binds to the vitamin D receptor (VDR), a member of the nuclear receptor super-family expressed in many cell types, and modulates a variety of biological functions. 1α, 25(OH)2D3 is essential for bone and mineral homeostasis, but also regulates growth and differentiation of multiple cell types, and displays immunoregulatory and anti-inflammatory activities. The antiproliferative, prodifferentiative, antibacterial, immunomodulatory and anti-inflammatory properties of synthetic VDR agonists could be exploited to treat a variety of chronic inflammatory and autoimmune diseases, including benign prostatic hyperplasia (BPH). It has been hypothesized that VDR may influence both the risk of a variety of diseases and their occurrence and prognosis. However, earlier studies investigating the associations between specific VDR polymorphisms and various diseases often show controversial results. We performed a systematic review of the current literature on vitamin D and BPH using the PubMed and Web of Knowledge databases. The aim of this review is to summarize the current knowledge on the utility of the VDR gene regarding prostate growth as well as the pathogenesis and treatment of BPH, a complex syndrome characterized by a static component related to prostate overgrowth, a dynamic component responsible for urinary storage symptoms, and an inflammatory component. Despite the massive advances in recent decades, further research is needed to fully characterize the exact underlying mechanisms of VDR action on BPH and to comprehend how these cellular changes translate into clinical development in physical concert. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3579114/ /pubmed/23450267 http://dx.doi.org/10.4103/0970-1591.105745 Text en Copyright: © Indian Journal of Urology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Manchanda, Parmeet Kaur Kibler, Aaron J Zhang, Mei Ravi, Janani Bid, Hemant K. Vitamin D receptor as a therapeutic target for benign prostatic hyperplasia |
title | Vitamin D receptor as a therapeutic target for benign prostatic hyperplasia |
title_full | Vitamin D receptor as a therapeutic target for benign prostatic hyperplasia |
title_fullStr | Vitamin D receptor as a therapeutic target for benign prostatic hyperplasia |
title_full_unstemmed | Vitamin D receptor as a therapeutic target for benign prostatic hyperplasia |
title_short | Vitamin D receptor as a therapeutic target for benign prostatic hyperplasia |
title_sort | vitamin d receptor as a therapeutic target for benign prostatic hyperplasia |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3579114/ https://www.ncbi.nlm.nih.gov/pubmed/23450267 http://dx.doi.org/10.4103/0970-1591.105745 |
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