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Association of Vascular Endothelial Growth Factor Gene Polymorphisms with Susceptibility and Clinicopathologic Characteristics of Colorectal Cancer

Since vascular endothelial growth factor (VEGF) is known to be a potent pro-angiogenic factor, we evaluated the potential association of two VEGF gene polymorphisms (-634G>C and 936C>T) with the susceptibility and the clinicopathologic characteristics of colorectal cancer (CRC). The VEGF genot...

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Autores principales: Chae, Yee Soo, Kim, Jong Gwang, Sohn, Sang Kyun, Cho, Yoon Young, Ahn, Byung Min, Moon, Joon Ho, Jeon, Seoung Woo, Park, Jae Yong, Lee, In Taek, Choi, Gyu Seog, Jun, Soo-Han
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2526538/
https://www.ncbi.nlm.nih.gov/pubmed/18583877
http://dx.doi.org/10.3346/jkms.2008.23.3.421
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author Chae, Yee Soo
Kim, Jong Gwang
Sohn, Sang Kyun
Cho, Yoon Young
Ahn, Byung Min
Moon, Joon Ho
Jeon, Seoung Woo
Park, Jae Yong
Lee, In Taek
Choi, Gyu Seog
Jun, Soo-Han
author_facet Chae, Yee Soo
Kim, Jong Gwang
Sohn, Sang Kyun
Cho, Yoon Young
Ahn, Byung Min
Moon, Joon Ho
Jeon, Seoung Woo
Park, Jae Yong
Lee, In Taek
Choi, Gyu Seog
Jun, Soo-Han
author_sort Chae, Yee Soo
collection PubMed
description Since vascular endothelial growth factor (VEGF) is known to be a potent pro-angiogenic factor, we evaluated the potential association of two VEGF gene polymorphisms (-634G>C and 936C>T) with the susceptibility and the clinicopathologic characteristics of colorectal cancer (CRC). The VEGF genotypes were determined using fresh colorectal tissue from 465 patients who had undergone a surgical resection and peripheral blood lymphocytes from 413 healthy controls by PCR/DHPLC assay. For the -634G>C polymorphism, the -634 GC or CC genotype was associated with a decreased risk of CRC (odds ratio [OR], 0.62; p=0.001) as a dominant model of C allele, whereas the 936 TT genotype correlated with advanced stage/ metastasis, a high serum level of CA19-9, and an higher grade in patients with CRC. In the haplotype analyses, haplotype -634C/936C and -634G/936T were associated with a decreased susceptibility of CRC (OR, 0.53 and 0.56; p<0.001, respectively). These observations imply that the VEGF gene polymorphisms may be associated with the susceptibility or clinicopathologic features of CRC. However, further studies of other VEGF sequence variants and their biological functions are needed to understand the role of the VEGF gene polymorphisms in the development and progression of CRC.
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spelling pubmed-25265382008-11-07 Association of Vascular Endothelial Growth Factor Gene Polymorphisms with Susceptibility and Clinicopathologic Characteristics of Colorectal Cancer Chae, Yee Soo Kim, Jong Gwang Sohn, Sang Kyun Cho, Yoon Young Ahn, Byung Min Moon, Joon Ho Jeon, Seoung Woo Park, Jae Yong Lee, In Taek Choi, Gyu Seog Jun, Soo-Han J Korean Med Sci Original Article Since vascular endothelial growth factor (VEGF) is known to be a potent pro-angiogenic factor, we evaluated the potential association of two VEGF gene polymorphisms (-634G>C and 936C>T) with the susceptibility and the clinicopathologic characteristics of colorectal cancer (CRC). The VEGF genotypes were determined using fresh colorectal tissue from 465 patients who had undergone a surgical resection and peripheral blood lymphocytes from 413 healthy controls by PCR/DHPLC assay. For the -634G>C polymorphism, the -634 GC or CC genotype was associated with a decreased risk of CRC (odds ratio [OR], 0.62; p=0.001) as a dominant model of C allele, whereas the 936 TT genotype correlated with advanced stage/ metastasis, a high serum level of CA19-9, and an higher grade in patients with CRC. In the haplotype analyses, haplotype -634C/936C and -634G/936T were associated with a decreased susceptibility of CRC (OR, 0.53 and 0.56; p<0.001, respectively). These observations imply that the VEGF gene polymorphisms may be associated with the susceptibility or clinicopathologic features of CRC. However, further studies of other VEGF sequence variants and their biological functions are needed to understand the role of the VEGF gene polymorphisms in the development and progression of CRC. The Korean Academy of Medical Sciences 2008-06 2008-06-20 /pmc/articles/PMC2526538/ /pubmed/18583877 http://dx.doi.org/10.3346/jkms.2008.23.3.421 Text en Copyright © 2008 The Korean Academy of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Chae, Yee Soo
Kim, Jong Gwang
Sohn, Sang Kyun
Cho, Yoon Young
Ahn, Byung Min
Moon, Joon Ho
Jeon, Seoung Woo
Park, Jae Yong
Lee, In Taek
Choi, Gyu Seog
Jun, Soo-Han
Association of Vascular Endothelial Growth Factor Gene Polymorphisms with Susceptibility and Clinicopathologic Characteristics of Colorectal Cancer
title Association of Vascular Endothelial Growth Factor Gene Polymorphisms with Susceptibility and Clinicopathologic Characteristics of Colorectal Cancer
title_full Association of Vascular Endothelial Growth Factor Gene Polymorphisms with Susceptibility and Clinicopathologic Characteristics of Colorectal Cancer
title_fullStr Association of Vascular Endothelial Growth Factor Gene Polymorphisms with Susceptibility and Clinicopathologic Characteristics of Colorectal Cancer
title_full_unstemmed Association of Vascular Endothelial Growth Factor Gene Polymorphisms with Susceptibility and Clinicopathologic Characteristics of Colorectal Cancer
title_short Association of Vascular Endothelial Growth Factor Gene Polymorphisms with Susceptibility and Clinicopathologic Characteristics of Colorectal Cancer
title_sort association of vascular endothelial growth factor gene polymorphisms with susceptibility and clinicopathologic characteristics of colorectal cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2526538/
https://www.ncbi.nlm.nih.gov/pubmed/18583877
http://dx.doi.org/10.3346/jkms.2008.23.3.421
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