Literature DB >> 15225833

Plasma levels of 25-hydroxyvitamin D, 1,25-dihydroxyvitamin D and the risk of prostate cancer.

Elizabeth T Jacobs1, Anna R Giuliano, María Elena Martínez, Bruce W Hollis, Mary E Reid, James R Marshall.   

Abstract

In the US, prostate cancer (PCa) has the highest incidence rate of all cancers in males, with few known modifiable risk factors. Some studies support an association between the Vitamin D metabolites, 1,25-dihydroxyvitamin D (1alpha,25(OH)(2)D(3)) and/or 25-hydroxyvitamin D (25(OH)D(3)), and prostate cancer, while others have yielded conflicting results. 1alpha,25(OH)(2)D(3) has anti-proliferative and pro-differentiating effects in prostate cancer cell lines, and levels of circulating 25(OH)D(3) may be important as PCa cells possess 1-alpha-hydroxylase activity. Using a nested case-control design, we evaluated whether plasma levels of 25(OH)D(3) and 1alpha,25(OH)(2)D(3) were associated with prostate cancer risk in participants from the Nutritional Prevention of Cancer (NPC) trial. With 83 cases and 166 matched controls, we calculated the adjusted odds ratios for increasing plasma levels of 25(OH)D(3) and 1alpha,25(OH)(2)D(3). Compared to the lowest tertile of plasma 25(OH)D(3) levels, the adjusted odds ratios were 1.71 (0.68-4.34) and 0.75 (0.29-1.91); the corresponding odds ratios for 1alpha,25(OH)(2)D(3) were 1.44 (0.59-3.52) and 1.06 (0.42-2.66). Given the pivotal effects of the Vitamin D receptor on gene transcription, it is likely that the anti-carcinogenic effects of Vitamin D that have previously been described are related to the activity and expression of the Vitamin D receptor and should be investigated further.

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Year:  2004        PMID: 15225833     DOI: 10.1016/j.jsbmb.2004.03.063

Source DB:  PubMed          Journal:  J Steroid Biochem Mol Biol        ISSN: 0960-0760            Impact factor:   4.292


  28 in total

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Authors:  Ruth C Travis; Aurora Perez-Cornago; Paul N Appleby; Demetrius Albanes; Corinne E Joshu; Pamela L Lutsey; Alison M Mondul; Elizabeth A Platz; Stephanie J Weinstein; Tracy M Layne; Kathy J Helzlsouer; Kala Visvanathan; Domenico Palli; Petra H Peeters; Bas Bueno-de-Mesquita; Antonia Trichopoulou; Marc J Gunter; Konstantinos K Tsilidis; Maria-Jose Sánchez; Anja Olsen; Hermann Brenner; Ben Schöttker; Laura Perna; Bernd Holleczek; Paul Knekt; Harri Rissanen; Bu B Yeap; Leon Flicker; Osvaldo P Almeida; Yuen Yee Elizabeth Wong; June M Chan; Edward L Giovannucci; Meir J Stampfer; Giske Ursin; Randi E Gislefoss; Tone Bjørge; Haakon E Meyer; Rune Blomhoff; Shoichiro Tsugane; Norie Sawada; Dallas R English; Darryl W Eyles; Alicia K Heath; Elizabeth J Williamson; Jonas Manjer; Johan Malm; Martin Almquist; Loic Le Marchand; Christopher A Haiman; Lynne R Wilkens; Jeannette M Schenk; Cathy M Tangen; Amanda Black; Michael B Cook; Wen-Yi Huang; Regina G Ziegler; Richard M Martin; Freddie C Hamdy; Jenny L Donovan; David E Neal; Mathilde Touvier; Serge Hercberg; Pilar Galan; Mélanie Deschasaux; Timothy J Key; Naomi E Allen
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7.  Effect of interval between serum draw and follow-up period on relative risk of cancer incidence with respect to 25-hydroxyvitamin D level: Implications for meta-analyses and setting vitamin D guidelines.

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9.  Serum levels of vitamin D metabolites and breast cancer risk in the prostate, lung, colorectal, and ovarian cancer screening trial.

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10.  Serum vitamin D and risk of prostate cancer in a case-control analysis nested within the European Prospective Investigation into Cancer and Nutrition (EPIC).

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Journal:  Am J Epidemiol       Date:  2009-04-09       Impact factor: 4.897

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