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Glutathione S-transferase enzymes are active in detoxifying a wide number of endogenous and exogenous chemical carcinogens and subsequently, are crucial in protecting the DNA. Several studies show some differences in association of glutathione S-transferase M1, T1 and P1 genetic polymorphisms with the risk of prostate cancer in various populations. The current study was done with Iranian subjects to evaluate the association of the polymorphism of glutathione S-transferase subtypes (T, M and P) and the susceptibility of prostate cancer in Iranian patients as compared to controls. Blood samples were collected from 65 prostate cancer patients and 65 unrelated health individuals as controls from Milad hospital, Tehran, Iran. The polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method was used to determine the polymorphism of glutathione S-transferase pi (GSTP1) -313 A/G gene, while multiplex PCR method was utilized to detect the glutathione S-transferase teta (GSTT) 1 and glutathione S-transferase mμ (GSTM) 1 null allele. There was no significant association in the -313 G allele (Val) of GSTP1 gene olymorphism and prostate cancer risk (odds ratio 0.61, 95% confidence intervals (CI) 0.08 - 4.60, p = 0.627). Moreover, no relationship was found between the polymorphism of GSTT1 (odds ratio 0.66, 95% CI 0.27 - 1.62) and GSTM1 (odds ratio 0.54, 95% CI 0.27 - 1.08) genes and higher risk of prostate cancer among Iranian subjects (p > 0.05). This study showed that either GSTP1-313 G polymorphism or GSTT1 and GSTM1 genes cannot be predisposing risk factors for prostate cancer among Iranian subjects.Key words: Glutathione S-transferase, prostate cancer, polymorphism.

Genetic polymorphisms were associated with an increase in the risk of developing disease and they are integral to the development of genetic marker to identify the individuals at risk. The genotypic distribution of various genetic polymorphisms involved in essential hypertension (EHT) and type 2 diabetes mellitus (T2DM) in Malaysian subjects has not been well characterized. The main objective of this study was to determine the association of S477X polymorphism of LPL gene, A6244G polymorphism of IRS-1 gene and C825T polymorphism of GN3 gene with EHT and T2DM in Malaysian subjects. This study includes 70 EHT, 60 T2DM, 65 EHT with T2DM and 75 control subjects. Genotyping of all the three polymorphisms was performed by PCR-RFLP method with the respective primers and restriction enzymes. The genotypic and allelic frequencies of the respective polymorphisms of the genes did not differ significantly (p>0.05) with EHT and T2DM in Malaysian subjects. The results of this study suggested that, S477X genotypes of LPL gene, A6244G genotypes of IRS-1 gene and C825Tgenotypes of GN3 gene was not associated with EHT and T2DM in Malaysian subjects.