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Genetic polymorphisms in DNA base excision repair gene XRCC1 and the risk of squamous cell carcinoma of the head and neck
BACKGROUND: The genes of base excision repair (BER) pathway have been extensively studied in the association with various human cancers. We performed a case-control study to test the association between two common single nucleotide polymorphisms (SNPs) of XRCC1 gene with human head and neck squamous...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2660298/ https://www.ncbi.nlm.nih.gov/pubmed/19284666 http://dx.doi.org/10.1186/1756-9966-28-37 |
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author | Kowalski, Michal Przybylowska, Karolina Rusin, Pawel Olszewski, Jurek Morawiec-Sztandera, Alina Bielecka-Kowalska, Anna Pietruszewska, Wioletta Mlynarski, Wojciech Szemraj, Janusz Majsterek, Ireneusz |
author_facet | Kowalski, Michal Przybylowska, Karolina Rusin, Pawel Olszewski, Jurek Morawiec-Sztandera, Alina Bielecka-Kowalska, Anna Pietruszewska, Wioletta Mlynarski, Wojciech Szemraj, Janusz Majsterek, Ireneusz |
author_sort | Kowalski, Michal |
collection | PubMed |
description | BACKGROUND: The genes of base excision repair (BER) pathway have been extensively studied in the association with various human cancers. We performed a case-control study to test the association between two common single nucleotide polymorphisms (SNPs) of XRCC1 gene with human head and neck squamous cell carcinoma (HNSCC). METHODS: The genotype analysis of Arg194Trp and Arg399Gln gene polymorphisms for 92 HNSCC patients and 124 controls of cancer free subjects, in Polish population were performed using the PCR-based restriction fragment length polymorphism (PCR-RFLP) with endonuclease MspI. RESULTS: No altered risk has been found individually for these SNPs, however haplotypes analysis showed high association with head and neck cancer. The highest frequency, according to wild-type of Arg194Arg and Arg399Arg genotypes, was identified for Arg194Trp-Arg399Arg haplotype (OR, 2.96; 95% CI, 1.01–8.80). CONCLUSION: Finally, we identified the combined Arg194Trp-Arg399Arg genotype of base excision repair gene XRCC1 that was associated with HNSCC and may have an impact on identification of a high-risk cancer population. |
format | Text |
id | pubmed-2660298 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26602982009-03-25 Genetic polymorphisms in DNA base excision repair gene XRCC1 and the risk of squamous cell carcinoma of the head and neck Kowalski, Michal Przybylowska, Karolina Rusin, Pawel Olszewski, Jurek Morawiec-Sztandera, Alina Bielecka-Kowalska, Anna Pietruszewska, Wioletta Mlynarski, Wojciech Szemraj, Janusz Majsterek, Ireneusz J Exp Clin Cancer Res Research BACKGROUND: The genes of base excision repair (BER) pathway have been extensively studied in the association with various human cancers. We performed a case-control study to test the association between two common single nucleotide polymorphisms (SNPs) of XRCC1 gene with human head and neck squamous cell carcinoma (HNSCC). METHODS: The genotype analysis of Arg194Trp and Arg399Gln gene polymorphisms for 92 HNSCC patients and 124 controls of cancer free subjects, in Polish population were performed using the PCR-based restriction fragment length polymorphism (PCR-RFLP) with endonuclease MspI. RESULTS: No altered risk has been found individually for these SNPs, however haplotypes analysis showed high association with head and neck cancer. The highest frequency, according to wild-type of Arg194Arg and Arg399Arg genotypes, was identified for Arg194Trp-Arg399Arg haplotype (OR, 2.96; 95% CI, 1.01–8.80). CONCLUSION: Finally, we identified the combined Arg194Trp-Arg399Arg genotype of base excision repair gene XRCC1 that was associated with HNSCC and may have an impact on identification of a high-risk cancer population. BioMed Central 2009-03-13 /pmc/articles/PMC2660298/ /pubmed/19284666 http://dx.doi.org/10.1186/1756-9966-28-37 Text en Copyright © 2009 Kowalski 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 Kowalski, Michal Przybylowska, Karolina Rusin, Pawel Olszewski, Jurek Morawiec-Sztandera, Alina Bielecka-Kowalska, Anna Pietruszewska, Wioletta Mlynarski, Wojciech Szemraj, Janusz Majsterek, Ireneusz Genetic polymorphisms in DNA base excision repair gene XRCC1 and the risk of squamous cell carcinoma of the head and neck |
title | Genetic polymorphisms in DNA base excision repair gene XRCC1 and the risk of squamous cell carcinoma of the head and neck |
title_full | Genetic polymorphisms in DNA base excision repair gene XRCC1 and the risk of squamous cell carcinoma of the head and neck |
title_fullStr | Genetic polymorphisms in DNA base excision repair gene XRCC1 and the risk of squamous cell carcinoma of the head and neck |
title_full_unstemmed | Genetic polymorphisms in DNA base excision repair gene XRCC1 and the risk of squamous cell carcinoma of the head and neck |
title_short | Genetic polymorphisms in DNA base excision repair gene XRCC1 and the risk of squamous cell carcinoma of the head and neck |
title_sort | genetic polymorphisms in dna base excision repair gene xrcc1 and the risk of squamous cell carcinoma of the head and neck |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2660298/ https://www.ncbi.nlm.nih.gov/pubmed/19284666 http://dx.doi.org/10.1186/1756-9966-28-37 |
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