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Association Between Gstm1 and Gstt1 Polymorphisms and Esophageal Squamous Cell Carcinoma: Results From a Case-Control Study in Kashmir, India Publisher Pubmed



Makhdoomi MA1, 2, 3, 4, 5 ; Shah IA1, 2, 3, 4, 5 ; Bhat GA1, 2, 3, 4, 5 ; Amin S1, 2, 3, 4, 5 ; Lone MM1, 2, 3, 4, 5 ; Islami F1, 2, 3, 4, 5 ; Dar NA1, 2, 3, 4, 5
Authors
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Authors Affiliations
  1. 1. Department of Biochemistry, University of Kashmir, Hazratbal Srinagar, 190006, JK, India
  2. 2. Department of Radiation Oncology, SK Institute of Medical Sciences, Soura Srinagar, 190011, India
  3. 3. Digestive Oncology Research Center, Digestive Disease Research Institute, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Institute for Transitional Epidemiology, Mount Sinai School of Medicine, New York, NY, United States
  5. 5. Surveillance and Health Services Research, American Cancer Society, Atlanta, GA, United States

Source: Tumor Biology Published:2015


Abstract

Polymorphisms in glutathione-S-transferases (GSTs), the phase II xenobiotic detoxifying enzymes, have been associated with increased cancer risk. In this study, we assessed the association of functional polymorphisms in GSTM1 and GSTT1 with esophageal cancer in Kashmir, India, an area with a high incidence of esophageal squamous cell carcinoma (ESCC). We analyzed genotypes of GSTM1 and GSTT1 using a multiplex PCR in 492 pairs of ESCC cases and individually matched controls. The associations between polymorphisms in these genes and ESCC risk were examined by conditional logistic regression models adjusted for multiple potential confounders. In addition, the interaction between these genes and several environmental exposures with regard to ESCC risk was assessed. Our results showed an association between the GSTT1 null genotype and ESCC risk (odds ratio (OR) = 1.58; 95 % confidence interval (CI) 1.04–2.39). Although GSTM1 alone was not associated with ESCC risk, individuals with the GSTM1−/GSTT1+ genotype showed an inverse relation with ESCC risk (OR = 0.55; 95 % CI 0.32–0.93), compared to GSTM1+/GSTT1+ individuals. We found a significant interaction between the GSTT1 and GSTM1 genotypes with regard to ESCC risk (P = 0.001); however, there were no interactions between environmental factors and GSTT1 and GSTM1 genotypes. This study indicates that GSTT1 null genotype is associated with ESCC risk in Kashmiri population. The association between GSTM1 and ESCC risk needs further investigations. Interactions of these genotypes with environmental exposures should be examined in multicentric studies with bigger sample sizes. © 2014, International Society of Oncology and BioMarkers (ISOBM).
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