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학술저널
저자정보
Anil, Sukumaran (Department of Preventive Dental Sciences, College of Dentistry, Prince Sattam Bin Abdulaziz University) Gopikrishnan, PB (Department of Conservative Dentistry and Endodontist, PSM College of Dental Sciences and Research) Basheer, Ashik Bin (Department of Oral and Maxillofacial Pathology, PSM College of Dental Sciences and Research) Vidyullatha, BG (Department of Oral and Maxillofacial Surgery and Diagnostic sciences, King Saud Bin Abdulaziz University for Health Sciences) Alogaibi, Yahya A (Department of Orthodontics, Faculty of Dentistry, King Abdulaziz University) Chalisserry, Elna P (Department of Maxillofacial Surgery & Diagnostic Sciences, College of Dentistry, College of Dentistry, Jazan University) Javed, Fawad (Department of General Dentistry, Eastman Institute for Oral Health, University of Rochester) Dalati, MHN (Consultant Orthodontist and Restorative Dentist, Springs Dental Care) Vellappally, Sajith (Dental Biomaterials Research Chair, Dental Health Department, College of Applied Medical Sciences, King Saud University) Hashem, Mohamed Ibrahim (Dental Biomaterials Research Chair, Dental Health Department, College of Applied Medica) Divakar, Darshan Devang
저널정보
아시아태평양암예방학회 Asian Pacific journal of cancer prevention : APJCP Asian Pacific journal of cancer prevention : APJCP 제17권 제8호
발행연도
2016.1
수록면
4,107 - 4,111 (5page)

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Background: Oral cancers account for approximately 2% of all cancers diagnosed each year; however, the vast majority (80%) of the affected individuals are smokers whose risk of developing a lesion is five to nine times greater than that of non-smokers. Tobacco smoke contains numerous carcinogens that cause DNA damage, including oxidative lesions that are removed effectively by the base-excision repair (BER) pathway, in which poly (ADP-ribose) polymerase 1 (PARP-1), plays key roles. Genetic variations in the genes encoding DNA repair enzymes may alter their functions. Several studies reported mixed effects on the association between PARP-1 variants and the risk of cancer development. Till now no reported studies have investigated the association between PARP-1 variants and oral squamous cell carcinoma (OSCC) risk in an Indian population. Materials and Methods: In the present case control study 100 OSCC patients and 100 matched controls were genotyped using PARP1 single nucleotide peptides (SNP's) rs1136410 and rs3219090 using TaqMan assays. Results: The results indicated significantly higher risk with PARP1 rs1136410 minor allele "C" (OR=1.909; p=0.02942; CI, 1.060-3.439). SNP rs1136410 also showed significantly increased risk in patients with smoking habit at C/C genotype and at minor allele C. Conclusions: The PAPR-1 Ala762Val polymorphism may play a role in progression of OSCC. Larger studies with a greater number of samples are needed to verify these findings.

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