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Genetic Association Between PER3 Genetic Polymorphisms and Cancer Susceptibility: A Meta-Analysis
The genes along the circadian pathways control and modulate circadian rhythms essential for the maintenance of physiological homeostasis through self-sustained transcription-translation feedback loops. PER3 (period 3) is a circadian pathway gene and its variants (rs1012477, 4/5-repeat) have frequent...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554033/ https://www.ncbi.nlm.nih.gov/pubmed/25837749 http://dx.doi.org/10.1097/MD.0000000000000568 |
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author | Geng, Peiliang Ou, Juanjuan Li, Jianjun Wang, Ning Xie, Ganfeng Sa, Rina Liu, Chen Xiang, Lisha Liang, Houjie |
author_facet | Geng, Peiliang Ou, Juanjuan Li, Jianjun Wang, Ning Xie, Ganfeng Sa, Rina Liu, Chen Xiang, Lisha Liang, Houjie |
author_sort | Geng, Peiliang |
collection | PubMed |
description | The genes along the circadian pathways control and modulate circadian rhythms essential for the maintenance of physiological homeostasis through self-sustained transcription-translation feedback loops. PER3 (period 3) is a circadian pathway gene and its variants (rs1012477, 4/5-repeat) have frequently been associated with human cancer. The mixed findings, however, make the role of the 2 variants in cancer susceptibility elusive. We aimed in this article to clarify the association of PER3 variants with cancer. We collected genetic data from 8 studies, providing 6149 individuals for rs1012477 and 5241 individuals for 4/5-repeat. Based on the genotype and allele frequency, we chose the fixed-effects model to estimate risk of cancer. Overall analysis did not suggest a global role of rs1012477 in cancer susceptibility. For PER3 4/5-repeat variant, we found a moderate increase in risk of cancer among individuals with the 5-allele compared to individuals with the 4-allele, although this association was not statistically significant (homozygous model: odds ratio [OR] 1.17, 95% confidence interval [CI] 0.81–1.67; recessive model: OR 1.17, 95% CI 0.82–1.67). No substantial heterogeneity was revealed in this analysis. Our meta-analysis provides no evidence supporting a global association of PER3 genetic variants with the incidence of cancer. |
format | Online Article Text |
id | pubmed-4554033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-45540332015-10-27 Genetic Association Between PER3 Genetic Polymorphisms and Cancer Susceptibility: A Meta-Analysis Geng, Peiliang Ou, Juanjuan Li, Jianjun Wang, Ning Xie, Ganfeng Sa, Rina Liu, Chen Xiang, Lisha Liang, Houjie Medicine (Baltimore) 5700 The genes along the circadian pathways control and modulate circadian rhythms essential for the maintenance of physiological homeostasis through self-sustained transcription-translation feedback loops. PER3 (period 3) is a circadian pathway gene and its variants (rs1012477, 4/5-repeat) have frequently been associated with human cancer. The mixed findings, however, make the role of the 2 variants in cancer susceptibility elusive. We aimed in this article to clarify the association of PER3 variants with cancer. We collected genetic data from 8 studies, providing 6149 individuals for rs1012477 and 5241 individuals for 4/5-repeat. Based on the genotype and allele frequency, we chose the fixed-effects model to estimate risk of cancer. Overall analysis did not suggest a global role of rs1012477 in cancer susceptibility. For PER3 4/5-repeat variant, we found a moderate increase in risk of cancer among individuals with the 5-allele compared to individuals with the 4-allele, although this association was not statistically significant (homozygous model: odds ratio [OR] 1.17, 95% confidence interval [CI] 0.81–1.67; recessive model: OR 1.17, 95% CI 0.82–1.67). No substantial heterogeneity was revealed in this analysis. Our meta-analysis provides no evidence supporting a global association of PER3 genetic variants with the incidence of cancer. Wolters Kluwer Health 2015-04-03 /pmc/articles/PMC4554033/ /pubmed/25837749 http://dx.doi.org/10.1097/MD.0000000000000568 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 5700 Geng, Peiliang Ou, Juanjuan Li, Jianjun Wang, Ning Xie, Ganfeng Sa, Rina Liu, Chen Xiang, Lisha Liang, Houjie Genetic Association Between PER3 Genetic Polymorphisms and Cancer Susceptibility: A Meta-Analysis |
title | Genetic Association Between PER3 Genetic Polymorphisms and Cancer Susceptibility: A Meta-Analysis |
title_full | Genetic Association Between PER3 Genetic Polymorphisms and Cancer Susceptibility: A Meta-Analysis |
title_fullStr | Genetic Association Between PER3 Genetic Polymorphisms and Cancer Susceptibility: A Meta-Analysis |
title_full_unstemmed | Genetic Association Between PER3 Genetic Polymorphisms and Cancer Susceptibility: A Meta-Analysis |
title_short | Genetic Association Between PER3 Genetic Polymorphisms and Cancer Susceptibility: A Meta-Analysis |
title_sort | genetic association between per3 genetic polymorphisms and cancer susceptibility: a meta-analysis |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554033/ https://www.ncbi.nlm.nih.gov/pubmed/25837749 http://dx.doi.org/10.1097/MD.0000000000000568 |
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