After lung cancer, prostate cancer has the highest mortality rate. Early and accurate diagnosis of this heterogeneous cancer promises more effective treatment. At present biopsy is the only definitive method of diagnosing the disease. Many gene loci are associated with increased susceptibility to this cancer. Here, the relationship between tumor necrosis factor alpha (TNF-α) gene variants and glucuronidation pathway gene variants with increased risk of prostate cancer in a population of Iranian men has been investigated.
Materials and methods:Blood samples were collected from 360 men including 120 healthy, 120 with benign prostate hyperplasia (BPH), and 120 patients with prostate cancer (PCa). DNA was extracted and tested for each variant with specific primers and PCR based methods. Data were analyzed using agarose and polyacrylamide gel electrophoresis, SPSS software, SNP Stats and Student's t-test.Results: UGT2B17 and UGT2B15 polymorphisms were associated with BPH in comparison to the control group (P value = <0.0001 and P value = 0.007). The only significant association in the cancer group was between G Score and UGT2B15, so that 90% of patients with PCa and G score less than or equal to 6, had GG genotype (0.01). Other variants had no significant relationship with the cause of the disease. Ins Del G haplotype was more common in BPH compared to the control group (P value = 0.011).