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https://hdl.handle.net/11499/6197
Title: | Frequencies of ADH1C alleles and genotypes ina Turkish head and neck cancer population | Authors: | Kortunay, S. Köseler, Aylin Kara, Cüneyt Orhan Topuz, Bülent Atalay, Erol Ömer |
Keywords: | alcohol dehydrogenase alcohol dehydrogenase 1C genomic DNA restriction endonuclease Sspl protein unclassified drug ADH1C protein, human adult aged article cell isolation clinical article controlled study disease association female gene frequency genetic variability genotype head and neck carcinoma head and neck squamous cell carcinoma human leukocyte male restriction fragment length polymorphism squamous cell carcinoma Turkey (republic) upper respiratory tract infection wild type allele case control study genetic polymorphism genetics head and neck tumor metabolism middle aged Adult Aged Alcohol Dehydrogenase Alleles Carcinoma, Squamous Cell Case-Control Studies Female Gene Frequency Genotype Head and Neck Neoplasms Humans Leukocytes Male Middle Aged Polymorphism, Genetic Polymorphism, Restriction Fragment Length Turkey Young Adult |
Abstract: | Squamous cell carcinoma of the head and neck (SCCHN) have been reported to be related to both genetic and environmental factors, including alcohol consumption and alcohol-metabolizing enzymes such as alcohol dehydrogenase (ADH). We conducted a hospital-based, case-control study including 50 cases with diagnosed SCCHN and 100 controls with non-neoplastic conditions such as upper respiratory tract infection. The genomic DNA was isolated from peripheral blood leukocytes. The ADH1C*1 wild-type and ADH1C*2 variant alleles were analyzed with an RFLP method by using SspI as restriction enzyme. The ADH1C*1 allele frequencies were 0.89 (CI95% = 0.84-0.91) in controls and 0.77 (CI95% = 0.71-0.83) in cases, and respective frequencies of the ADH1C*2 allele were 0.11 (CI95% = 0.07-0.14) and 0.23 (CI95% = 0.17-0.29) among controls and cases (P = 0.01). The ADH1C*1/*1 genotype frequency was significantly higher in the control group (77%) compared to that of the cases (58%) (P = 0.02).These findings suggest that a lower presence of ADH1C*1 allele is associated with SCCHN, but larger numbers are needed to more precisely estimate the interaction, if any, with ADH1C. Interestingly, the ADH1C allele and genotype frequencies in our control group living in Denizli were significantly different compared to a previously published report from healthy volunteers living in Ankara (P < 0.0001). © 2010 Prous Science, S.A.U. or its licensors. | URI: | https://hdl.handle.net/11499/6197 https://doi.org/10.1358/mf.2010.32.3.1440739 |
ISSN: | 0379-0355 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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