Association of CYP1A1, GSTM1 and GSTT1 gene polymorphisms with risk of prostate cancer in Algerian population

• Published in: African journal of urology 2020-12, Vol.26 (1), p.44-8, Article 44
• Main Authors: Medjani, Somia, Chellat-Rezgoune, Djalila, Kezai, Taher, Chidekh, Mohammed, Abadi, Noureddine, Satta, Dalila
• Format: Article
• Language: English
• Subjects: Cancer; Cytochrome P-450; Cytochrome P4501A1 T3801C; Development and progression; Disease susceptibility; Enzymes; Genes; Genetic aspects; Genetic polymorphism; Genetic polymorphisms; Genetic research; Glutathione S-transferase (GST), GSTM1, GSTT, PCR-RFLP, multiplex PCR; Glutathione transferase; Health aspects; Health care; Imaging; Medicine; Medicine & Public Health; Metabolism; Oncology, Experimental; Original Research; Physiological aspects; Polymorphism; Prostate cancer; Radiology; Regression analysis; Risk factors; Smoking; Statistical analysis; Surgery; Tobacco; Urology; Xenobiotics
• ISSN: 1110-5704; 1961-9987
• DOI: 10.1186/s12301-020-00049-2

Background Prostate cancer is the most common cancer in the world, and its etiology involves the interaction of genetic and environmental factors. Interindividual differences observed in the metabolism of xenobiotics may be due to polymorphisms of genes encoding the detoxification enzymes. This genetic variability seems to be associated with differences in susceptibility to certain types of cancers, including prostate cancer. Our study has been made in order to investigate a possible genetic predisposition to prostate cancer in an Algerian population, through the analysis of genetic polymorphisms of three enzymes metabolizing xenobiotics namely cytochrome P450 (CYP) 1A1, glutathione S - transferase mu 1 ( GSTM1 ) and GST theta 1 (GSTT1). Methods The current case–control study included 101 prostate cancer patients and 101 healthy controls. Genotyping of CYP1A1 T3801C polymorphisms and GSTM1/GSTT - null was made, respectively, by PCR-RFLP and multiplex PCR. Results No significantly positive associations were found for the CYP1A1 T3801C [ p  = 0.71, OR = 1.23 (0.56–2.72)] and GSTM1 - null [ p  = 0.26, OR = 1.37 (0.76–2.4)] polymorphisms and prostate cancer susceptibility. However, we detect a highly significant association between GSTT1 - null genotype [ p  = 0.03, OR = 2.03 (1.06–3.99)], GSTM1/GSTT1 -double null genotype [ p  = 0.027, OR = 2.6; CI (1.07–6.5)] and prostate cancer risk. Furthermore, no statistically significant differences between the studied polymorphisms and tumor parameters (the Gleason score and clinical stages of aggressiveness) at diagnosis of PCa. Conclusions The risk of developing prostate cancer in Algeria does not appear to be associated with CYP1A1 T3801C genotypes and GSTM1 - null , but GSTT1 - null and GSTM1/GSTT1 -double null genotypes increased the risk of prostate cancer.