Research Article

The Association of Polymorphisms in Nrf2 and Genes Involved in Redox Homeostasis in the Development and Progression of Clear Cell Renal Cell Carcinoma

Table 3

Combined effect of Nrf2, SOD2, GPX1, and GSTP1 genotypes in relation to the risk of ccRCC carriers of at least one variant allele.

GenotypesNrf2 (rs6721961)SOD2 (rs4880)GSTP1 (rs1695)GSTP1 (rs1138272)
C/CcC/A and A/AdAla/AlaeAla/Val and Val/ValfIle/IleiIle/Val+Val/ValjAla/AlakAla/Val+Val/Vall

Nrf2 (rs6721961) C/Cc
 OR (95% CI)a1.00b3.211 (1.513-6.814)1.00b1.067 (0.41-2.779)
0.0020.894
Nrf2 (rs6721961) C/A and A/Ad
 OR (95% CI)a0.385 (0.095-1.564)2.731 (1.107-6.739)0.835 (0.430-1.621)0.162 (0.019-1.408)
0.1820.0290.5940.099
SOD2 (rs4880) Ala/Alae
 OR (95% CI)a1.00b0.308 (0.059-1.599)1.00b4.796 (0.927-24.81)1.00b0.594 (0.064-5.504)
0.1610.0620.646
SOD2 (rs4880) Ala/Val and Val/Valf
 OR (95% CI)a3.234 (1.436-7.280)2.918 (1.131-7.532)5.875 (1.190-29.00)19.724 (4.267-91.16)4.374 (2.012-9.508)3.290 (1.054-10.26)
0.0050.0270.030<0.001<0.0010.040
GPX1 (rs1050450) Pro/Prog
 OR (95% CI)a1.00b0.423 (0.158-1.133)1.00b3.653 (1.148-11.63)1.00b5.476 (2.127-14.10)1.00b0.826 (0.238-2.868)
0.0870.028<0.0010.763
GPX1 (rs1050450) Pro/Leu and Leu/Leuh
 OR (95% CI)a0.440 (0.223-0.868)0.456 (0.188-1.057)0.553 (0.144-2.120)2.533 (0.793-8.094)0.720 (0.239-2.165)2.194 (0.912-5.287)0.585 (0.322-1.063)0.372 (0.115-1.199)
0.0180.0670.3880.1170.5580.0790.0790.098

aOR: odds ratio adjusted for age, gender, BMI, pack-years, and hypertension; CI: confidence interval; breference group; cC/C: carriers of both referent alleles; dC/A and A/A: carriers of both referent alleles; eAla/Ala: carriers of both referent alleles; fAla/Val and Val/Val: carriers of at least one variant allele; gPro/Pro: carriers of both referent alleles; hPro/Leu and Leu/Leu: carriers of at least one variant allele; iIle/Ile: carriers of both referent alleles; jIle/Val and Val/Val: carriers of at least one variant allele; kAla/Ala: carriers of both referent alleles; lAla/Val and Val/Val: carriers of at least one variant allele.