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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...

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Autores principales: Kowalski, Michal, Przybylowska, Karolina, Rusin, Pawel, Olszewski, Jurek, Morawiec-Sztandera, Alina, Bielecka-Kowalska, Anna, Pietruszewska, Wioletta, Mlynarski, Wojciech, Szemraj, Janusz, Majsterek, Ireneusz
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
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.
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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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