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ALDH3B2 Polymorphism Is Associated with Colorectal Cancer Susceptibility

Colorectal cancer (CRC) is the 5(th) leading cancer in China. Alcohol consumption has been reported to be one of the risk factors of CRC. However, it remains unclear whether genetic variants of alcohol metabolic genes are associated with CRC risk. In this study, we tested the coding variants in the...

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Autores principales: Gao, Zhi-Gang, Yang, Yong, Han, Xiao-Feng, Wang, Yun-Lei, Wang, Zhen-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7199530/
https://www.ncbi.nlm.nih.gov/pubmed/32377192
http://dx.doi.org/10.1155/2020/5179635
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author Gao, Zhi-Gang
Yang, Yong
Han, Xiao-Feng
Wang, Yun-Lei
Wang, Zhen-Jun
author_facet Gao, Zhi-Gang
Yang, Yong
Han, Xiao-Feng
Wang, Yun-Lei
Wang, Zhen-Jun
author_sort Gao, Zhi-Gang
collection PubMed
description Colorectal cancer (CRC) is the 5(th) leading cancer in China. Alcohol consumption has been reported to be one of the risk factors of CRC. However, it remains unclear whether genetic variants of alcohol metabolic genes are associated with CRC risk. In this study, we tested the coding variants in the alcohol metabolic genes and the risk of CRC, by using 485 cases and 516 controls. A total of 16 germline coding variants in 10 alcohol metabolic genes were genotyped. We identified that rs3741178 in ALDH3B2 was significantly associated with CRC risk with odds ratio being 2.13 (95% CI: 1.24–3.68, P=0.0064). Further functional annotation suggested that this variant may damage the protein function of ALDH3B2. Our results suggested that ALDH3B2 in the alcohol metabolism pathway contributed to the development of CRC, which may contribute to the prevention of this disease in the future.
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spelling pubmed-71995302020-05-06 ALDH3B2 Polymorphism Is Associated with Colorectal Cancer Susceptibility Gao, Zhi-Gang Yang, Yong Han, Xiao-Feng Wang, Yun-Lei Wang, Zhen-Jun J Oncol Research Article Colorectal cancer (CRC) is the 5(th) leading cancer in China. Alcohol consumption has been reported to be one of the risk factors of CRC. However, it remains unclear whether genetic variants of alcohol metabolic genes are associated with CRC risk. In this study, we tested the coding variants in the alcohol metabolic genes and the risk of CRC, by using 485 cases and 516 controls. A total of 16 germline coding variants in 10 alcohol metabolic genes were genotyped. We identified that rs3741178 in ALDH3B2 was significantly associated with CRC risk with odds ratio being 2.13 (95% CI: 1.24–3.68, P=0.0064). Further functional annotation suggested that this variant may damage the protein function of ALDH3B2. Our results suggested that ALDH3B2 in the alcohol metabolism pathway contributed to the development of CRC, which may contribute to the prevention of this disease in the future. Hindawi 2020-01-04 /pmc/articles/PMC7199530/ /pubmed/32377192 http://dx.doi.org/10.1155/2020/5179635 Text en Copyright © 2020 Zhi-Gang Gao et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gao, Zhi-Gang
Yang, Yong
Han, Xiao-Feng
Wang, Yun-Lei
Wang, Zhen-Jun
ALDH3B2 Polymorphism Is Associated with Colorectal Cancer Susceptibility
title ALDH3B2 Polymorphism Is Associated with Colorectal Cancer Susceptibility
title_full ALDH3B2 Polymorphism Is Associated with Colorectal Cancer Susceptibility
title_fullStr ALDH3B2 Polymorphism Is Associated with Colorectal Cancer Susceptibility
title_full_unstemmed ALDH3B2 Polymorphism Is Associated with Colorectal Cancer Susceptibility
title_short ALDH3B2 Polymorphism Is Associated with Colorectal Cancer Susceptibility
title_sort aldh3b2 polymorphism is associated with colorectal cancer susceptibility
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7199530/
https://www.ncbi.nlm.nih.gov/pubmed/32377192
http://dx.doi.org/10.1155/2020/5179635
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