GSTM1 GSTT1 and GSTP1 Genetic Variants in Multiple Urologic Cancers
D. N. Chirilă, R. Popp, Ș. Vesa, O. Bălăcescu, I. Coman, N. A. Constantea, C. CiuceOriginal article, no. 3, 2015
Introduction: Glutathione S-transferases (GSTs) are phase 2enzymes responsible for catalyzing the biotransformation of awide variety of electrophilic compounds, having a crucial rolein the detoxification of active metabolites of procarcinogens produced by phase 1 reactions, tying them to glutathione and promoting their excretion in the urine.
Objectives: we evaluated GSTM1, GSTT1 and GSTP1 genotypesin patients diagnosed with multiple malignancies, ofwhich at least one was found in the prostate, bladder orkidney.
Materials and methods: GSTM1, GSTT1 and GSTP1 genotypeswere genetically assessed in 34 patients with multiple urologiccancers and 23 patients with urologic cancer associated with another type of cancer.
Results: in the group of patients with multiple urologic cancers,GSTT1 null genotype was found in 26.4% of patientscompared to 0% in controls, 82.35 % of patients and 47% of witnesses carried at least one GSTM1 or GSTT1 null genotype, and in the group with different cancers, GSTM1 null genotype was found in 52.1% of patients compared to 4.3% witnesses in the control group; GSTT1 null genotype wasfound in 34.7% of patients compared to 4.3% of witnesses, atleast one GSTM1 or GSTT1 null genotype was found in73.9% of patients compared to 8.6% of controls.
Conclusions: GSTT1 null genotype is a risk factor for patients with more primitive urologic malignancies (bladder, prostate and kidney); GSTM1 or GSTT1 null genotype is more frequent in patients with multiple urologic tumors; GSTM1and GSTT1 null genotypes are risk factors in patients with different types of cancer, with at least one affecting the urinarysystem.



