GSTT1, GSTM1, and CYP1B1 gene polymorphisms and susceptibility to sporadic renal cell cancer

作者:Salinas Sanchez Antonio S*; Sanchez Sanchez Francisco; Donate Moreno Maria J; Rubio del Campo Antonio; Serrano Oviedo Leticia; Gimenez Bachs Jose M; Martinez Sanchiz Carlos; Segura Martin Miguel; Escribano Julio
来源:Urologic Oncology-Seminars and Original Investigations, 2012, 30(6): 864-870.
DOI:10.1016/j.urolonc.2010.10.001

摘要

Purpose: To estimate the prevalence and importance of GSTT1, GSTM1, and CYP1B1 genotypes in renal cell carcinoma (RCC), and to identify their value as a prognostic factor. %26lt;br%26gt;Materials and methods: Cross-sectional study of a group of patients diagnosed with RCC (n = 133) and a control group (n = 208) with benign conditions and no history of tumor. Controls were selected by cumulative samples and mixed pairing. All subjects pertained to the catchment area for our hospital. Sociodemographic variables, anatomical pathology features, and presence of GSTT1, GSTM1, and CYP1B1 polymorphisms by multiplex PCR and sequencing techniques. %26lt;br%26gt;Results: There were no differences in the genotype distribution of the GSTT1 and GSTM1 genes between cases and controls. In the case of CYP1B1, the GO genotype (Ala119) was more prevalent in patients with RCC (OR = 2.08; 95% Cl: 1.32-2.28) and may be implicated in 34.3% (95% Cl: 16.3-52.2) of RCCs. In patients with GSTT I deletion, TNM stages III to IV were more common (39.1%); whereas in Val432 homozygous patients in CYP1B1, Fuhrman grades 3 to 4 (54.6%) were more common. Because this was a cross-sectional study, longitudinal studies are needed in the future to confirm these data. %26lt;br%26gt;Conclusions: No relationship between GSTT1 and GSTM1 genotypes and RCC risk was observed. Homozygous subjects with Ala 1 19 in CYP1B1 had twice the risk of RCC as homozygous for Ser119 or heterozygotes. Patients with GSTT1 deletion had tumors of more advanced stages, and those with Val432 polymorphism in CYP1B1 had tumors of higher Fuhrman grade.

  • 出版日期2012-12