GSTM1 and GSTT1 polymorphism and susceptibility to esophageal cancer in high- and low-risk regions of India

被引:16
|
作者
Sharma, Anita [1 ]
Das, Bhudev Chander [2 ]
Sehgal, Ashok [3 ]
Mehrotra, Ravi [4 ]
Kar, Premashish [5 ]
Sardana, Sarita [3 ]
Phukan, Rup [6 ]
Mahanta, Jagdish [6 ]
Purkayastha, Joydeep [7 ]
Saxena, Sunita [8 ]
Kapur, Sujala [8 ]
Chatterjee, Indranil [9 ]
Sharma, Joginder Kumar [1 ]
机构
[1] Inst Cytol & Prevent Oncol ICMR, Div Mol Diagnost, Noida 201301, India
[2] Univ Delhi, BR Ambedkar Ctr Biomed Res, Delhi 11007, India
[3] Inst Cytol & Prevent Oncol ICMR, Div Epidemiol & Biostat, Noida 201301, India
[4] Inst Cytol & Prevent Oncol ICMR, Noida 201301, India
[5] Maulana Azad Med Coll, Dept Med, New Delhi 110002, India
[6] Reg Med Res Ctr, Dibrugarh 786001, Assam, India
[7] Dr Bhubaneswar Borooah Canc Inst BBCI, Gauhati 781016, Assam, India
[8] Safdarjang Hosp, Natl Inst Pathol ICMR, New Delhi 110029, India
[9] Roswell Pk Canc Inst, Canc Genet Dept, Buffalo, NY 14263 USA
关键词
Glutathione transferase; Polymorphism; GSTM1; GSTT1; Esophageal cancer; GLUTATHIONE-S-TRANSFERASE; SQUAMOUS-CELL CARCINOMA; GENETIC POLYMORPHISMS; METABOLIZING ENZYMES; CYTOCHROME-P450; 2E1; GASTRIC-CANCER; LUNG-CANCER; CYP1A1; POPULATION; CHINA;
D O I
10.1007/s13277-013-0897-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glutathione transferases, a super family of dimeric phase II metabolic enzymes play a vital role in biotransformation of many substances. This study evaluates the influence of genetic polymorphism of GSTM1 and GSTT1 gene loci on esophageal cancer risk in Assam and Delhi from India. DNA from blood samples of esophageal cancer cases (203,112) and controls (286,150) from Assam and Delhi, respectively, were extracted. GSTM1 and GSTT1 polymorphisms were analyzed by multiplex PCR procedure. Differences in proportions were tested using Pearson's chi-square test with odds ratio (OR) and 95 % confidence interval (CI). Risk of esophageal cancer was approximately twice in individuals having homozygous GSTM1 (OR-2.1, 95 % CI, 1.44-3.13) and GSTT1 null genotypes (OR-1.7,95 % CI, 0.99-2.77) in Assam, and around three times in GSTT1 null genotype (OR-2.9, 95 % CI, 1.56-5.27) in Delhi population. GSTM1 null genotype seems to play a protective role (OR-0.7, 95 % CI, 0.39-1.27) in Delhi. A significant association of GSTM1 null genotype with esophageal cancer was observed in a younger age group in Assam (OR-2.7, 95 % CI, 1.48-5.01), and in Delhi population association was observed in smokers with GSTT1 null genotype (OR-2.5, 95 % CI, 1.04-6.07), and alcoholics having GSTM1 null genotype (OR-2.6, 95 % CI, 0.99-6.77). Significant association of GSTM1 null genotype in Assam was observed between cancer cases and controls in fermented betel nut chewers only (OR-2.8, 95 % CI, 1.19-6.72), whereas, smoking and alcohol failed to show any correlation with GSTM1/GSTT1 genotypes. Cancer development is not only due to exogenous or endogenous carcinogens but depends on their interaction with genes that are involved in the detoxification of these carcinogens.
引用
收藏
页码:3249 / 3257
页数:9
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