TY - JOUR ID - 32519 TI - Roles of CYP1A1 and CYP2E1 Gene Polymorphisms in Oral Submucous Fibrosis JO - Asian Pacific Journal of Cancer Prevention JA - APJCP LA - en SN - 1513-7368 AU - Yaming, Punyo AU - Urs, Aadithya Basavaraj AU - Saxena, Alpana AU - Zuberi, Mariyam AD - Department of Oral Pathology and Microbiology, Maulana Azad Institute of Dental Sciences, New Delhi, India Email : draadithyaburs@gmail.com AD - Y1 - 2016 PY - 2016 VL - 17 IS - 7 SP - 3335 EP - 3340 DO - N2 - Background: Oral submucous fibrosis (OSF) is a precancerous condition with a 4 to13% malignant transformation rate. Related to the habit of areca nut chewing it is mainly prevalent in Southeast Asian countries where the habit of betel quid chewing is frequently practised. On chewing, alkaloids and polyphenols are released which undergo nitrosation and give rise to Nnitrosamines which are cytotoxic agents. CYP450 is a microsomal enzyme group which metabolizes various endogenous and exogenous chemicals including those released by areca nut chewing. CYP1A1 plays a central role in metabolic activation of these xenobiotics, whereas CYP2E1 metabolizes nitrosamines and tannins. Polymorphisms in genes that code for these enzymes may alter their expression or function and may therefore affect an individuals susceptibility regarding OSF and oral cancer. The present study was therefore undertaken to investigate the association of polymorphisms in CYP1A1 m2 and CYP2E1 (RsaI/PstI) sites with risk of OSF among areca nut chewers in the Northern India population. A total of 95 histopathologically confirmed cases of OSF with history of areca nut chewing not less than 1 year and 80, age and sex matched controls without any clinical signs and symptoms of OSF with areca nut chewing habit not less than 1 year were enrolled. DNA was extracted from peripheral blood samples and polymorphisms were analyzed by PCRRFLP method. Gene polymorphism of CYP1A1 at NcoI site was observed to be significantly higher (p 0.016) in cases of OSF when compared to controls. Association of CYP1A1 gene polymorphism at NcoI site and the risk of OSF (Odds Ratio 2.275) was also observed to be significant. However, no such association was observed for the CYP2E1 gene polymorphism (Odds Ratio 0.815). Our results suggest that the CYP1A1 gene polymorphism at the NcoI site confers an increased risk for OSF. UR - https://journal.waocp.org/article_32519.html L1 - https://journal.waocp.org/article_32519_e08c1ab16f35cf0a6338de90ff0a4d51.pdf ER -