DNA repair gene ERCC2 polymorphisms and risk of squamous cell carcinoma of the head and neck
Autor: | Thomas C. Wascher, Gerhard Friedrich, Markus Gugatschka, Wilfried Renner, Dadbeh Dehchamani |
---|---|
Rok vydání: | 2010 |
Předmět: |
Male
DNA Repair DNA repair Clinical Biochemistry Single-nucleotide polymorphism Biology Polymorphism Single Nucleotide Pathology and Forensic Medicine XRCC1 XRCC3 Gene Frequency Risk Factors Genotype Carcinoma medicine Odds Ratio Humans Genetic Predisposition to Disease Molecular Biology Allele frequency Aged Xeroderma Pigmentosum Group D Protein Homozygote Middle Aged medicine.disease stomatognathic diseases Head and Neck Neoplasms Cancer research Carcinoma Squamous Cell ERCC2 Female |
Zdroj: | Experimental and molecular pathology. 91(1) |
ISSN: | 1096-0945 |
Popis: | Introduction Genetic aberrations of DNA repair enzymes are known to be common events and to be associated with different cancer entities. Aim of the following study was to analyze the genetic association of single nucleotide polymorphisms (SNP) of the DNA repair genes with the risk of squamous cell carcinoma of the head and neck (HNSCC). Materials and methods Genetic variants ERCC2 Lys751Gln (rs13181), ERCC2 Asp312Asn (rs1799793), XRCC1 Arg194Trp (rs1799782); XRCC1 Gln399Arg (rs25487), XRCC1 Arg280His (rs25489) and XRCC3 Thr241Met (rs861539) were analyzed in a primary study group comprising 169 patients with histologically confirmed HNSCC and 463 healthy control subjects. Polymorphisms associated with HNSCC were furthermore analyzed in an independent replication study including 125 HNSCC. Results Only the ERCC2 751 Gln/Gln genotype was associated with HNSCC in the primary study ( p = 0.033) and in the replication study ( p = 0.023), resulting in an overall odds ratio of 0.54 (95% confidence interval 0.35–0.92; p = 0.006). Conclusion Carriers of the homozygous ERCC2 751 Gln/Gln genotype may be at lower risk for HNSCC. |
Databáze: | OpenAIRE |
Externí odkaz: |