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Association between interleukin-22 genetic polymorphisms and bladder cancer risk
OBJECTIVE: The cytokine interleukin-22 (IL-22), which is produced by T cells and natural killer cells, is associated with tumorigenesis and tumor progression in cancers. However, the role of IL-22 in bladder cancer has not been investigated. MATERIALS AND METHODS: A prospective hospital-based case-c...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602377/ https://www.ncbi.nlm.nih.gov/pubmed/26598081 http://dx.doi.org/10.6061/clinics/2015(10)05 |
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author | Zhao, Tao Wu, XiaoHou Liu, JiaJi |
author_facet | Zhao, Tao Wu, XiaoHou Liu, JiaJi |
author_sort | Zhao, Tao |
collection | PubMed |
description | OBJECTIVE: The cytokine interleukin-22 (IL-22), which is produced by T cells and natural killer cells, is associated with tumorigenesis and tumor progression in cancers. However, the role of IL-22 in bladder cancer has not been investigated. MATERIALS AND METHODS: A prospective hospital-based case-control study comprising 210 patients with pathologically proven bladder cancer and 210 age- and gender-matched healthy controls was conducted. The genotypes of 3 common polymorphisms (-429 C/T, +1046 T/A and +1995 A/C) of the IL-22 gene were determined with fluorogenic 5' exonuclease assays. RESULTS: Patients with bladder cancer had a significantly higher frequency of the IL-22 -429 TT genotype [odds ratio (OR)=2.04, 95% confidence interval (CI)=1.19, 3.49; p=0.009] and -429 T allele (OR=1.42, 95% CI=1.08, 1.87; p=0.01) than the healthy controls. These findings were still significant after a Bonferroni correction. When stratifying according to the stage of bladder cancer, we found that patients with superficial bladder cancer had a significantly lower frequency of the IL-22 -429 TT genotype (OR=0.48, 95% CI=0.23, 0.98; p=0.04). When stratifying according to the grade and histological type of bladder cancer, we found no statistical association. The IL-22 +1046 T/A and IL-22 +1995 A/C gene polymorphisms were not associated with the risk of bladder cancer. CONCLUSION: To the authors' knowledge, this is the first report documenting that the IL-22 -429 C/T gene polymorphism is associated with bladder cancer risk. Additional studies are required to confirm this finding. |
format | Online Article Text |
id | pubmed-4602377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo |
record_format | MEDLINE/PubMed |
spelling | pubmed-46023772015-12-07 Association between interleukin-22 genetic polymorphisms and bladder cancer risk Zhao, Tao Wu, XiaoHou Liu, JiaJi Clinics (Sao Paulo) Clinical Science OBJECTIVE: The cytokine interleukin-22 (IL-22), which is produced by T cells and natural killer cells, is associated with tumorigenesis and tumor progression in cancers. However, the role of IL-22 in bladder cancer has not been investigated. MATERIALS AND METHODS: A prospective hospital-based case-control study comprising 210 patients with pathologically proven bladder cancer and 210 age- and gender-matched healthy controls was conducted. The genotypes of 3 common polymorphisms (-429 C/T, +1046 T/A and +1995 A/C) of the IL-22 gene were determined with fluorogenic 5' exonuclease assays. RESULTS: Patients with bladder cancer had a significantly higher frequency of the IL-22 -429 TT genotype [odds ratio (OR)=2.04, 95% confidence interval (CI)=1.19, 3.49; p=0.009] and -429 T allele (OR=1.42, 95% CI=1.08, 1.87; p=0.01) than the healthy controls. These findings were still significant after a Bonferroni correction. When stratifying according to the stage of bladder cancer, we found that patients with superficial bladder cancer had a significantly lower frequency of the IL-22 -429 TT genotype (OR=0.48, 95% CI=0.23, 0.98; p=0.04). When stratifying according to the grade and histological type of bladder cancer, we found no statistical association. The IL-22 +1046 T/A and IL-22 +1995 A/C gene polymorphisms were not associated with the risk of bladder cancer. CONCLUSION: To the authors' knowledge, this is the first report documenting that the IL-22 -429 C/T gene polymorphism is associated with bladder cancer risk. Additional studies are required to confirm this finding. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2015-10 2015-10 /pmc/articles/PMC4602377/ /pubmed/26598081 http://dx.doi.org/10.6061/clinics/2015(10)05 Text en Copyright © 2015 CLINICS http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Science Zhao, Tao Wu, XiaoHou Liu, JiaJi Association between interleukin-22 genetic polymorphisms and bladder cancer risk |
title | Association between interleukin-22 genetic polymorphisms and bladder cancer risk |
title_full | Association between interleukin-22 genetic polymorphisms and bladder cancer risk |
title_fullStr | Association between interleukin-22 genetic polymorphisms and bladder cancer risk |
title_full_unstemmed | Association between interleukin-22 genetic polymorphisms and bladder cancer risk |
title_short | Association between interleukin-22 genetic polymorphisms and bladder cancer risk |
title_sort | association between interleukin-22 genetic polymorphisms and bladder cancer risk |
topic | Clinical Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602377/ https://www.ncbi.nlm.nih.gov/pubmed/26598081 http://dx.doi.org/10.6061/clinics/2015(10)05 |
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