Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1782182378476666880 |
---|---|
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. |
format | Text |
id | pubmed-2885363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT wangshujie associationbetweenegf61gaandgliomariskinachinesepopulation AT zhaoyao associationbetweenegf61gaandgliomariskinachinesepopulation AT ruanzhenchao associationbetweenegf61gaandgliomariskinachinesepopulation AT chenhongyan associationbetweenegf61gaandgliomariskinachinesepopulation AT fanweiwei associationbetweenegf61gaandgliomariskinachinesepopulation AT chenjuxiang associationbetweenegf61gaandgliomariskinachinesepopulation AT wuqihan associationbetweenegf61gaandgliomariskinachinesepopulation AT qianji associationbetweenegf61gaandgliomariskinachinesepopulation AT zhangtianbao associationbetweenegf61gaandgliomariskinachinesepopulation AT huangyan associationbetweenegf61gaandgliomariskinachinesepopulation AT ludaru associationbetweenegf61gaandgliomariskinachinesepopulation |