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Kallikrein 3 and vitamin D receptor polymorphisms: potentials environmental risk factors for prostate cancer

OBJECTIVE: To investigate the relationship and interaction of the single nucleotide polymorphisms (SNPs) of KLK3 and VDR and environmental factors with the predisposition to prostate cancer within Chinese population. METHODS: The comparison between 108 patients and 242 healthy people was carried out...

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Autores principales: Hu, Jianpeng, Qiu, Zhen, Zhang, Liansheng, Cui, Feilun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022449/
https://www.ncbi.nlm.nih.gov/pubmed/24755043
http://dx.doi.org/10.1186/1746-1596-9-84
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author Hu, Jianpeng
Qiu, Zhen
Zhang, Liansheng
Cui, Feilun
author_facet Hu, Jianpeng
Qiu, Zhen
Zhang, Liansheng
Cui, Feilun
author_sort Hu, Jianpeng
collection PubMed
description OBJECTIVE: To investigate the relationship and interaction of the single nucleotide polymorphisms (SNPs) of KLK3 and VDR and environmental factors with the predisposition to prostate cancer within Chinese population. METHODS: The comparison between 108 patients and 242 healthy people was carried out by using the TaqMan/MGB Probe Technology to determine the genotypes of KLK3(rs2735839 is located between KLK2 and KLK3) and VDR (rs731236 is located exon 9). Univariate and multivariate logistic regression model were used to assess the connection of genetic polymorphisms and environmental risk factors with PCa by collecting demographic information, as well as BMI, consumption of cigarettes, alcohol, and tea, exercise, and other environmental risk factors. RESULTS: The appearing frequencies of AA, AG, and GG genotypes at the SNPs rs2735839 (A/G) for KLK3 were 13.89%, 62.96% and 23.15% in PCa and 37.19%, 44.63%, 18.18% in control, respectively; these two groups are statistically different (P = 0.00). While the appearing frequencies of TT, TC, and CC genotypes at the SNPs rs731236 (T/C) for VDR were 88.89%, 9, 26%, 1.85% and 90.50%, 9.10%, 0.40% in control, respectively, with no significant statistical difference between the two group. The study confirmed decreasing risk in tea drinkers (OR = 0.58, 95% CI = 0.35-0.96). CONCLUSIONS: Our studies indicate that environmental factor-tea drinking is associated with the development of PCa. The habit of drinking tea is a protective factor against PCa. The SNPs rs2735839 for KLK3 is strongly related to the development of PCa, while the SNPs rs731236 for VDR is not. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/9759981571058803.
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spelling pubmed-40224492014-05-16 Kallikrein 3 and vitamin D receptor polymorphisms: potentials environmental risk factors for prostate cancer Hu, Jianpeng Qiu, Zhen Zhang, Liansheng Cui, Feilun Diagn Pathol Research OBJECTIVE: To investigate the relationship and interaction of the single nucleotide polymorphisms (SNPs) of KLK3 and VDR and environmental factors with the predisposition to prostate cancer within Chinese population. METHODS: The comparison between 108 patients and 242 healthy people was carried out by using the TaqMan/MGB Probe Technology to determine the genotypes of KLK3(rs2735839 is located between KLK2 and KLK3) and VDR (rs731236 is located exon 9). Univariate and multivariate logistic regression model were used to assess the connection of genetic polymorphisms and environmental risk factors with PCa by collecting demographic information, as well as BMI, consumption of cigarettes, alcohol, and tea, exercise, and other environmental risk factors. RESULTS: The appearing frequencies of AA, AG, and GG genotypes at the SNPs rs2735839 (A/G) for KLK3 were 13.89%, 62.96% and 23.15% in PCa and 37.19%, 44.63%, 18.18% in control, respectively; these two groups are statistically different (P = 0.00). While the appearing frequencies of TT, TC, and CC genotypes at the SNPs rs731236 (T/C) for VDR were 88.89%, 9, 26%, 1.85% and 90.50%, 9.10%, 0.40% in control, respectively, with no significant statistical difference between the two group. The study confirmed decreasing risk in tea drinkers (OR = 0.58, 95% CI = 0.35-0.96). CONCLUSIONS: Our studies indicate that environmental factor-tea drinking is associated with the development of PCa. The habit of drinking tea is a protective factor against PCa. The SNPs rs2735839 for KLK3 is strongly related to the development of PCa, while the SNPs rs731236 for VDR is not. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/9759981571058803. BioMed Central 2014-04-22 /pmc/articles/PMC4022449/ /pubmed/24755043 http://dx.doi.org/10.1186/1746-1596-9-84 Text en Copyright © 2014 Hu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research
Hu, Jianpeng
Qiu, Zhen
Zhang, Liansheng
Cui, Feilun
Kallikrein 3 and vitamin D receptor polymorphisms: potentials environmental risk factors for prostate cancer
title Kallikrein 3 and vitamin D receptor polymorphisms: potentials environmental risk factors for prostate cancer
title_full Kallikrein 3 and vitamin D receptor polymorphisms: potentials environmental risk factors for prostate cancer
title_fullStr Kallikrein 3 and vitamin D receptor polymorphisms: potentials environmental risk factors for prostate cancer
title_full_unstemmed Kallikrein 3 and vitamin D receptor polymorphisms: potentials environmental risk factors for prostate cancer
title_short Kallikrein 3 and vitamin D receptor polymorphisms: potentials environmental risk factors for prostate cancer
title_sort kallikrein 3 and vitamin d receptor polymorphisms: potentials environmental risk factors for prostate cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022449/
https://www.ncbi.nlm.nih.gov/pubmed/24755043
http://dx.doi.org/10.1186/1746-1596-9-84
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