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Effects of genetic variations in the Adiponectin pathway genes on the risk of colorectal cancer in the Chinese population

BACKGROUND: Decreased expression of adiponectin (ADIPOQ) is associated with an increased risk for developing colorectal cancer (CRC) in humans. This study was designed to determine whether polymorphisms present in the ADIPOQ and its type 1 receptor (ADIPOR1) could affect the risk of CRC. METHODS: We...

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Autores principales: He, Bangshun, Pan, Yuqin, Zhang, Ying, Bao, Qian, Chen, Liping, Nie, Zhenlin, Gu, Ling, Xu, Yeqiong, Wang, Shukui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166913/
https://www.ncbi.nlm.nih.gov/pubmed/21749709
http://dx.doi.org/10.1186/1471-2350-12-94
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author He, Bangshun
Pan, Yuqin
Zhang, Ying
Bao, Qian
Chen, Liping
Nie, Zhenlin
Gu, Ling
Xu, Yeqiong
Wang, Shukui
author_facet He, Bangshun
Pan, Yuqin
Zhang, Ying
Bao, Qian
Chen, Liping
Nie, Zhenlin
Gu, Ling
Xu, Yeqiong
Wang, Shukui
author_sort He, Bangshun
collection PubMed
description BACKGROUND: Decreased expression of adiponectin (ADIPOQ) is associated with an increased risk for developing colorectal cancer (CRC) in humans. This study was designed to determine whether polymorphisms present in the ADIPOQ and its type 1 receptor (ADIPOR1) could affect the risk of CRC. METHODS: We measured five polymorphisms in the ADIPOQ and two polymorphisms in ADIPOR1, and analyzed their associations with CRC risk in 420 CRC patients and 555 age- and gender-matched healthy individuals. RESULTS: Multivariate logistic regression analyses revealed that the CRC risks (adjusted odds ratio and 95% confidence interval) associated with the ADIPOR1 genotypes were 0.53 (95% CI, 0.35-0.81) for rs12733285C/T, 0.59 (95% CI, 0.45-0.78) for rs1342387A/G, and 0.59 (95% CI, 0.39-0.89) for rs1342387A/A, respectively. Furthermore, the risks were more significant in carriers of the allele A of rs1342387A/G (adjusted OR, 0.59; 95% CI, 0.46-0.77) than noncarriers (G/G). In a further subgroup analysis, we observed that rs266729G/C was associated with an increased risk for colon cancer (adjusted OR, 1.50; 95% CI, 1.05-2.14) but not for rectal cancer (adjusted OR, 0.88; 95% CI, 0.63-1.22), and that carriers of the G allele had an increased risk for developing colon cancer (adjusted OR, 1.45; 95% CI, 1.03-2.05). CONCLUSIONS: We conclude that the rs12733285C/T genotype and the carriage of the A allele of rs1342387 (A/G or A/A) in ADIPOR1 are the protective factors for CRC, while that rs266729G/C and G allele of ADIPOQ are the risk factors for colon cancer after excluding rectal cancer cases.
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spelling pubmed-31669132011-09-06 Effects of genetic variations in the Adiponectin pathway genes on the risk of colorectal cancer in the Chinese population He, Bangshun Pan, Yuqin Zhang, Ying Bao, Qian Chen, Liping Nie, Zhenlin Gu, Ling Xu, Yeqiong Wang, Shukui BMC Med Genet Research Article BACKGROUND: Decreased expression of adiponectin (ADIPOQ) is associated with an increased risk for developing colorectal cancer (CRC) in humans. This study was designed to determine whether polymorphisms present in the ADIPOQ and its type 1 receptor (ADIPOR1) could affect the risk of CRC. METHODS: We measured five polymorphisms in the ADIPOQ and two polymorphisms in ADIPOR1, and analyzed their associations with CRC risk in 420 CRC patients and 555 age- and gender-matched healthy individuals. RESULTS: Multivariate logistic regression analyses revealed that the CRC risks (adjusted odds ratio and 95% confidence interval) associated with the ADIPOR1 genotypes were 0.53 (95% CI, 0.35-0.81) for rs12733285C/T, 0.59 (95% CI, 0.45-0.78) for rs1342387A/G, and 0.59 (95% CI, 0.39-0.89) for rs1342387A/A, respectively. Furthermore, the risks were more significant in carriers of the allele A of rs1342387A/G (adjusted OR, 0.59; 95% CI, 0.46-0.77) than noncarriers (G/G). In a further subgroup analysis, we observed that rs266729G/C was associated with an increased risk for colon cancer (adjusted OR, 1.50; 95% CI, 1.05-2.14) but not for rectal cancer (adjusted OR, 0.88; 95% CI, 0.63-1.22), and that carriers of the G allele had an increased risk for developing colon cancer (adjusted OR, 1.45; 95% CI, 1.03-2.05). CONCLUSIONS: We conclude that the rs12733285C/T genotype and the carriage of the A allele of rs1342387 (A/G or A/A) in ADIPOR1 are the protective factors for CRC, while that rs266729G/C and G allele of ADIPOQ are the risk factors for colon cancer after excluding rectal cancer cases. BioMed Central 2011-07-12 /pmc/articles/PMC3166913/ /pubmed/21749709 http://dx.doi.org/10.1186/1471-2350-12-94 Text en Copyright ©2011 He 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 cited.
spellingShingle Research Article
He, Bangshun
Pan, Yuqin
Zhang, Ying
Bao, Qian
Chen, Liping
Nie, Zhenlin
Gu, Ling
Xu, Yeqiong
Wang, Shukui
Effects of genetic variations in the Adiponectin pathway genes on the risk of colorectal cancer in the Chinese population
title Effects of genetic variations in the Adiponectin pathway genes on the risk of colorectal cancer in the Chinese population
title_full Effects of genetic variations in the Adiponectin pathway genes on the risk of colorectal cancer in the Chinese population
title_fullStr Effects of genetic variations in the Adiponectin pathway genes on the risk of colorectal cancer in the Chinese population
title_full_unstemmed Effects of genetic variations in the Adiponectin pathway genes on the risk of colorectal cancer in the Chinese population
title_short Effects of genetic variations in the Adiponectin pathway genes on the risk of colorectal cancer in the Chinese population
title_sort effects of genetic variations in the adiponectin pathway genes on the risk of colorectal cancer in the chinese population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166913/
https://www.ncbi.nlm.nih.gov/pubmed/21749709
http://dx.doi.org/10.1186/1471-2350-12-94
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