Please use this identifier to cite or link to this item: 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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