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CXCL12-G801A polymorphism modulates risk of colorectal cancer in Taiwan

INTRODUCTION: The chemokine CXCL12, designated stromal cell-derived factor-1 (SDF-1), plays a significant role in many cancer metastases. Previous studies have shown that CXCL12-G801A, a single nucleotide polymorphism (SNP) in the 3’ untranslated region, correlates with breast and lung cancer in Ira...

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Autores principales: Shi, Ming-Der, Chen, Jing-Hsien, Sung, Hsin-Te, Lee, Jung-Shin, Tsai, Li-Yu, Lin, Hui-Hsuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902706/
https://www.ncbi.nlm.nih.gov/pubmed/24482642
http://dx.doi.org/10.5114/aoms.2013.39211
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author Shi, Ming-Der
Chen, Jing-Hsien
Sung, Hsin-Te
Lee, Jung-Shin
Tsai, Li-Yu
Lin, Hui-Hsuan
author_facet Shi, Ming-Der
Chen, Jing-Hsien
Sung, Hsin-Te
Lee, Jung-Shin
Tsai, Li-Yu
Lin, Hui-Hsuan
author_sort Shi, Ming-Der
collection PubMed
description INTRODUCTION: The chemokine CXCL12, designated stromal cell-derived factor-1 (SDF-1), plays a significant role in many cancer metastases. Previous studies have shown that CXCL12-G801A, a single nucleotide polymorphism (SNP) in the 3’ untranslated region, correlates with breast and lung cancer in Iran. The aim of this study was to evaluate the association of the gene variant CXCL12-G801A with colorectal cancer (CRC) in a Taiwanese cohort. MATERIAL AND METHODS: In this study, we used a denaturing high performance liquid chromatography (DHPLC) method to analyze the frequencies of CXCL12-G801A polymorphic variants between CRC patients (n = 258) and healthy controls (n = 300) in Taiwan. RESULTS: The SNP distribution was higher in CRC patients with TNM stage II (117/258) than healthy controls (52/300). We observed a significant increase in the G/A plus A/A genotype of the CXCL12-G801A polymorphism in CRC patients (45.35%) compared with healthy controls (17.33%). The analysis of allelic frequencies in both groups revealed that CRC patients have a higher frequency of A allele (23.45%) than healthy controls (8.67%). Furthermore, among older CRC patients, the frequency of the CXCL12-G801A genotype was significantly increased (p = 0.0148). CONCLUSIONS: Our observations suggest that the CXCL12-G801A genotype may be associated with some clinical manifestations in CRC patients in Taiwan.
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spelling pubmed-39027062014-01-30 CXCL12-G801A polymorphism modulates risk of colorectal cancer in Taiwan Shi, Ming-Der Chen, Jing-Hsien Sung, Hsin-Te Lee, Jung-Shin Tsai, Li-Yu Lin, Hui-Hsuan Arch Med Sci Basic Research INTRODUCTION: The chemokine CXCL12, designated stromal cell-derived factor-1 (SDF-1), plays a significant role in many cancer metastases. Previous studies have shown that CXCL12-G801A, a single nucleotide polymorphism (SNP) in the 3’ untranslated region, correlates with breast and lung cancer in Iran. The aim of this study was to evaluate the association of the gene variant CXCL12-G801A with colorectal cancer (CRC) in a Taiwanese cohort. MATERIAL AND METHODS: In this study, we used a denaturing high performance liquid chromatography (DHPLC) method to analyze the frequencies of CXCL12-G801A polymorphic variants between CRC patients (n = 258) and healthy controls (n = 300) in Taiwan. RESULTS: The SNP distribution was higher in CRC patients with TNM stage II (117/258) than healthy controls (52/300). We observed a significant increase in the G/A plus A/A genotype of the CXCL12-G801A polymorphism in CRC patients (45.35%) compared with healthy controls (17.33%). The analysis of allelic frequencies in both groups revealed that CRC patients have a higher frequency of A allele (23.45%) than healthy controls (8.67%). Furthermore, among older CRC patients, the frequency of the CXCL12-G801A genotype was significantly increased (p = 0.0148). CONCLUSIONS: Our observations suggest that the CXCL12-G801A genotype may be associated with some clinical manifestations in CRC patients in Taiwan. Termedia Publishing House 2013-11-29 2013-12-30 /pmc/articles/PMC3902706/ /pubmed/24482642 http://dx.doi.org/10.5114/aoms.2013.39211 Text en Copyright © 2013 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Basic Research
Shi, Ming-Der
Chen, Jing-Hsien
Sung, Hsin-Te
Lee, Jung-Shin
Tsai, Li-Yu
Lin, Hui-Hsuan
CXCL12-G801A polymorphism modulates risk of colorectal cancer in Taiwan
title CXCL12-G801A polymorphism modulates risk of colorectal cancer in Taiwan
title_full CXCL12-G801A polymorphism modulates risk of colorectal cancer in Taiwan
title_fullStr CXCL12-G801A polymorphism modulates risk of colorectal cancer in Taiwan
title_full_unstemmed CXCL12-G801A polymorphism modulates risk of colorectal cancer in Taiwan
title_short CXCL12-G801A polymorphism modulates risk of colorectal cancer in Taiwan
title_sort cxcl12-g801a polymorphism modulates risk of colorectal cancer in taiwan
topic Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902706/
https://www.ncbi.nlm.nih.gov/pubmed/24482642
http://dx.doi.org/10.5114/aoms.2013.39211
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