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Association between EGF +61 G/A and glioma risk in a Chinese population

BACKGROUND: Epidermal growth factor (EGF) is critical in cancer process. EGF and EGF receptor (EGFR) interaction plays a pivotal role in cell proliferation, differentiation, and tumorigenesis of epithelial tissues. Variations of the EGF +61G/A (rs4444903) may lead to an alteration in EGF production...

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Autores principales: Wang, Shujie, Zhao, Yao, Ruan, Zhenchao, Chen, Hongyan, Fan, Weiwei, Chen, Juxiang, Wu, Qihan, Qian, Ji, Zhang, Tianbao, Huang, Yan, Lu, Daru
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2885363/
https://www.ncbi.nlm.nih.gov/pubmed/20487573
http://dx.doi.org/10.1186/1471-2407-10-221
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author Wang, Shujie
Zhao, Yao
Ruan, Zhenchao
Chen, Hongyan
Fan, Weiwei
Chen, Juxiang
Wu, Qihan
Qian, Ji
Zhang, Tianbao
Huang, Yan
Lu, Daru
author_facet Wang, Shujie
Zhao, Yao
Ruan, Zhenchao
Chen, Hongyan
Fan, Weiwei
Chen, Juxiang
Wu, Qihan
Qian, Ji
Zhang, Tianbao
Huang, Yan
Lu, Daru
author_sort Wang, Shujie
collection PubMed
description BACKGROUND: Epidermal growth factor (EGF) is critical in cancer process. EGF and EGF receptor (EGFR) interaction plays a pivotal role in cell proliferation, differentiation, and tumorigenesis of epithelial tissues. Variations of the EGF +61G/A (rs4444903) may lead to an alteration in EGF production and/or activity, which can result in individual susceptibility to brain glioma. The purpose of this study was to investigate the potential association between EGF +61G/A and brain glioma in a Chinese population. METHODS: In this study, we analyzed single nucleotide polymorphism of EGF +61G/A in 677 patients with glioma and 698 gender- and age-matched controls. Genotyping was performed by polymerase chain reaction-ligation detection reaction (PCR-LDR) method. RESULTS: The A allele (minor Allele) was 33.0% in cases and 27.3% in controls. The additive model was more powerful to reveal the association in our study than that of recessive and dominant model. Our data showed the genotype G/A and A/A was associated with increased risk for glioma (adjusted OR = 1.48, 95%CI: 1.17-1.87, p = 0.001 for G/A, adjusted OR = 1.81, 95%CI: 1.20-2.72, p = 0.005 for A/A, respectively), and for glioblastoma (adjusted OR = 1.51, 95%CI: 1.06-2.17, p = 0.024 and adjusted OR = 2.35, 95%CI: 1.34-4.15, p = 0.003, respectively). The A allele significantly increased glioma risk (OR = 1.31, 95%CI: 1.11-1.55, p = 0.001). The additive model (G/G vs G/A vs A/A) showed that both G/A and A/A genotype increased glioma risk (adjusted OR = 1.40, 95% CI: 1.17-1.66, p = 0.0002).G/A and A/A genotypes or EGF +61 A allele increased risk in both low and high WHO grade glioma. Non-smokers with G/A and A/A genotype showed increased glioma risk compared with G/G genotype (adjusted OR = 1.72, 95%CI: 1.29-2.30, p = 0.0002 and adjusted OR = 1.81, 95%CI: 1.10-2.99, p = 0.020, respectively). This association was not found in ever- or current-smokers. CONCLUSIONS: Our study indicated that G/A and A/A genotypes or EGF +61 A allele were associated with higher glioma risk in Chinese. This is in contrast with previous studies which reported G allele as a risk factor of glioma in Caucasian. The role of EGF +61 A/G polymorphism in glioma susceptibility needs further investigation.
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spelling pubmed-28853632010-06-15 Association between EGF +61 G/A and glioma risk in a Chinese population Wang, Shujie Zhao, Yao Ruan, Zhenchao Chen, Hongyan Fan, Weiwei Chen, Juxiang Wu, Qihan Qian, Ji Zhang, Tianbao Huang, Yan Lu, Daru BMC Cancer Research Article BACKGROUND: Epidermal growth factor (EGF) is critical in cancer process. EGF and EGF receptor (EGFR) interaction plays a pivotal role in cell proliferation, differentiation, and tumorigenesis of epithelial tissues. Variations of the EGF +61G/A (rs4444903) may lead to an alteration in EGF production and/or activity, which can result in individual susceptibility to brain glioma. The purpose of this study was to investigate the potential association between EGF +61G/A and brain glioma in a Chinese population. METHODS: In this study, we analyzed single nucleotide polymorphism of EGF +61G/A in 677 patients with glioma and 698 gender- and age-matched controls. Genotyping was performed by polymerase chain reaction-ligation detection reaction (PCR-LDR) method. RESULTS: The A allele (minor Allele) was 33.0% in cases and 27.3% in controls. The additive model was more powerful to reveal the association in our study than that of recessive and dominant model. Our data showed the genotype G/A and A/A was associated with increased risk for glioma (adjusted OR = 1.48, 95%CI: 1.17-1.87, p = 0.001 for G/A, adjusted OR = 1.81, 95%CI: 1.20-2.72, p = 0.005 for A/A, respectively), and for glioblastoma (adjusted OR = 1.51, 95%CI: 1.06-2.17, p = 0.024 and adjusted OR = 2.35, 95%CI: 1.34-4.15, p = 0.003, respectively). The A allele significantly increased glioma risk (OR = 1.31, 95%CI: 1.11-1.55, p = 0.001). The additive model (G/G vs G/A vs A/A) showed that both G/A and A/A genotype increased glioma risk (adjusted OR = 1.40, 95% CI: 1.17-1.66, p = 0.0002).G/A and A/A genotypes or EGF +61 A allele increased risk in both low and high WHO grade glioma. Non-smokers with G/A and A/A genotype showed increased glioma risk compared with G/G genotype (adjusted OR = 1.72, 95%CI: 1.29-2.30, p = 0.0002 and adjusted OR = 1.81, 95%CI: 1.10-2.99, p = 0.020, respectively). This association was not found in ever- or current-smokers. CONCLUSIONS: Our study indicated that G/A and A/A genotypes or EGF +61 A allele were associated with higher glioma risk in Chinese. This is in contrast with previous studies which reported G allele as a risk factor of glioma in Caucasian. The role of EGF +61 A/G polymorphism in glioma susceptibility needs further investigation. BioMed Central 2010-05-21 /pmc/articles/PMC2885363/ /pubmed/20487573 http://dx.doi.org/10.1186/1471-2407-10-221 Text en Copyright ©2010 Wang 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
Wang, Shujie
Zhao, Yao
Ruan, Zhenchao
Chen, Hongyan
Fan, Weiwei
Chen, Juxiang
Wu, Qihan
Qian, Ji
Zhang, Tianbao
Huang, Yan
Lu, Daru
Association between EGF +61 G/A and glioma risk in a Chinese population
title Association between EGF +61 G/A and glioma risk in a Chinese population
title_full Association between EGF +61 G/A and glioma risk in a Chinese population
title_fullStr Association between EGF +61 G/A and glioma risk in a Chinese population
title_full_unstemmed Association between EGF +61 G/A and glioma risk in a Chinese population
title_short Association between EGF +61 G/A and glioma risk in a Chinese population
title_sort association between egf +61 g/a and glioma risk in a chinese population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2885363/
https://www.ncbi.nlm.nih.gov/pubmed/20487573
http://dx.doi.org/10.1186/1471-2407-10-221
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