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Association study between XPG Asp1104His polymorphism and colorectal cancer risk in a Chinese population
Previous studies have reported that the Asp1104His polymorphism in Xeroderma Pigmentosum complementation group G (XPG) was associated with the susceptibility to colorectal cancer (CRC), although the results were inconsistent. This study was aim to investigate whether there existed an association bet...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4204027/ https://www.ncbi.nlm.nih.gov/pubmed/25332048 http://dx.doi.org/10.1038/srep06700 |
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author | Du, Haina Zhang, Xizhi Du, Mulong Guo, Nannan Chen, Zhipeng Shu, Yongqian Zhang, Zhengdong Wang, Meilin Zhu, Lingjun |
author_facet | Du, Haina Zhang, Xizhi Du, Mulong Guo, Nannan Chen, Zhipeng Shu, Yongqian Zhang, Zhengdong Wang, Meilin Zhu, Lingjun |
author_sort | Du, Haina |
collection | PubMed |
description | Previous studies have reported that the Asp1104His polymorphism in Xeroderma Pigmentosum complementation group G (XPG) was associated with the susceptibility to colorectal cancer (CRC), although the results were inconsistent. This study was aim to investigate whether there existed an association between XPG Asp1104His polymorphism and CRC risk in the Chinese population, and a further meta-analysis was performed to consolidate the results. We found that XPG Asp1104His polymorphism was associated with a significantly increased CRC risk (dominant model: His/His + Asp/His vs. Asp/Asp, adjusted OR = 1.39, 95% CI = 1.14–1.69). Stratification analysis by clinical characteristics indicated that the His/His + Asp/His genotypes were associated with increased CRC susceptibility in patients with moderately differentiated grade, but not in poorly and well differentiated grade. Furthermore, a total of 5 eligible studies, including 2,649 CRC cases and 2,848 controls, were recruited for the meta-analysis. We identified that the meta-analysis reported a similar result in dominant model (OR = 1.35; 95% CI = 1.20–1.51). Especially, when stratified by ethnicity, an evidently increased risk was identified in the Asian population. In conclusion, our findings suggest that XPG Asp1104His polymorphism may increase the susceptibility of CRC, especially in Asian populations. |
format | Online Article Text |
id | pubmed-4204027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42040272014-10-21 Association study between XPG Asp1104His polymorphism and colorectal cancer risk in a Chinese population Du, Haina Zhang, Xizhi Du, Mulong Guo, Nannan Chen, Zhipeng Shu, Yongqian Zhang, Zhengdong Wang, Meilin Zhu, Lingjun Sci Rep Article Previous studies have reported that the Asp1104His polymorphism in Xeroderma Pigmentosum complementation group G (XPG) was associated with the susceptibility to colorectal cancer (CRC), although the results were inconsistent. This study was aim to investigate whether there existed an association between XPG Asp1104His polymorphism and CRC risk in the Chinese population, and a further meta-analysis was performed to consolidate the results. We found that XPG Asp1104His polymorphism was associated with a significantly increased CRC risk (dominant model: His/His + Asp/His vs. Asp/Asp, adjusted OR = 1.39, 95% CI = 1.14–1.69). Stratification analysis by clinical characteristics indicated that the His/His + Asp/His genotypes were associated with increased CRC susceptibility in patients with moderately differentiated grade, but not in poorly and well differentiated grade. Furthermore, a total of 5 eligible studies, including 2,649 CRC cases and 2,848 controls, were recruited for the meta-analysis. We identified that the meta-analysis reported a similar result in dominant model (OR = 1.35; 95% CI = 1.20–1.51). Especially, when stratified by ethnicity, an evidently increased risk was identified in the Asian population. In conclusion, our findings suggest that XPG Asp1104His polymorphism may increase the susceptibility of CRC, especially in Asian populations. Nature Publishing Group 2014-10-21 /pmc/articles/PMC4204027/ /pubmed/25332048 http://dx.doi.org/10.1038/srep06700 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Du, Haina Zhang, Xizhi Du, Mulong Guo, Nannan Chen, Zhipeng Shu, Yongqian Zhang, Zhengdong Wang, Meilin Zhu, Lingjun Association study between XPG Asp1104His polymorphism and colorectal cancer risk in a Chinese population |
title | Association study between XPG Asp1104His polymorphism and colorectal cancer risk in a Chinese population |
title_full | Association study between XPG Asp1104His polymorphism and colorectal cancer risk in a Chinese population |
title_fullStr | Association study between XPG Asp1104His polymorphism and colorectal cancer risk in a Chinese population |
title_full_unstemmed | Association study between XPG Asp1104His polymorphism and colorectal cancer risk in a Chinese population |
title_short | Association study between XPG Asp1104His polymorphism and colorectal cancer risk in a Chinese population |
title_sort | association study between xpg asp1104his polymorphism and colorectal cancer risk in a chinese population |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4204027/ https://www.ncbi.nlm.nih.gov/pubmed/25332048 http://dx.doi.org/10.1038/srep06700 |
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