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. 2017 Feb 8;8(12):19298–19309. doi: 10.18632/oncotarget.15197

Table 2. Genetic variants in the RhoA/ROCK1 pathway associated with the PCa risk.

Genetic Variants Case (n = 830) Control (n = 869) Pa Adjusted OR (95% CI)b
n % n %
RhoA rs2410
AA 199 24.0 233 26.8 0.059 1.00 (reference)
AC 378 45.5 415 47.8 0.591 1.06 (0.84–1.35)
CC 253 30.5 221 25.4 0.028 1.11 (1.01–1.21)
AC+CC 631 76.0 636 73.2 0.180 1.11 (1.02–1.21)
A allele 776 46.8 881 50.7 0.022 1.00 (reference)
C allele 884 53.2 857 49.3 1.18 (1.03–1.35)
RhoA rs2625955
AA 325 39.2 348 40.1 0.849 1.00 (reference)
AC 376 45.3 394 45.3 0.938 0.99 (0.80–1.22)
CC 129 15.5 127 14.6 0.567 1.01 (0.92–1.12)
AC+CC 505 60.8 521 59.9 0.708 1.01 (0.92–1.12)
A allele 1026 61.8 1090 62.7 0.585 1.00 (reference)
C allele 634 38.2 648 37.2 1.01 (0.88–1.17)
RhoA rs2269736
AA 186 22.4 116 13.3 < 0.001 1.00 (reference)
AG 399 48.1 404 46.5 < 0.001 0.63 (0.48–0.82)
GG 245 29.5 349 40.2 < 0.001 0.76 (0.69–0.83)
AG+GG 644 77.6 753 86.7 < 0.001 0.79 (0.72–0.86)
A allele 771 46.5 636 36.6 < 0.001 1.00 (reference)
G allele 889 53.5 1102 63.4 0.66 (0.57–0.76)
ROCK1 rs11874761
AA 12 1.4 11 1.3 0.914 1.00 (reference)
AG 169 20.4 182 20.9 0.708 0.80 (0.34–1.90)
GG 649 78.2 676 77.8 0.761 0.93 (0.71–1.23)
AG+GG 818 98.6 858 98.7 0.748 0.99 (0.88–1.11)
A allele 193 11.6 204 11.7 0.920 1.00 (reference)
G allele 1467 88.4 1534 88.3 0.97 (0.79–1.20)
ROCK1 rs35996865
GG 16 1.9 15 1.8 0.140 1.00 (reference)
GT 179 21.6 155 17.8 0.833 1.03 (0.48–2.18)
TT 635 76.5 699 80.4 0.658 0.94 (0.74–1.20)
GT+TT 814 98.1 854 98.2 0.756 0.89 (0.80–0.99)
G allele 211 12.7 185 10.6 0.061 1.00 (reference)
T allele 1449 87.3 1553 89.4 0.80 (0.65–0.99)
ROCK1 rs8089974
GG 8 1.0 14 1.6 0.119 1.00 (reference)
GT 174 20.9 153 17.6 0.126 2.01 (0.80–5.08)
TT 648 78.1 702 80.8 0.278 1.16 (0.86–1.56)
GT+TT 822 99.0 855 98.4 0.238 0.93 (0.83–1.04)
G allele 190 11.5 181 10.4 0.335 1.00 (reference)
T allele 1470 88.5 1557 89.6 0.89 (0.71–1.10)

Bold values indicated significant differences between two groups.

aTwo-sided χ2 test for either genotype distributions or allele frequencies between the cases and controls. All P values were Bonferroni corrected, and statistical significance was set at P < 0.01667 (0.05/3).

bAdjusted for age, bmi, pack-years of smoking, drinking status, tea drinking, hypertension and diabetes in logistic regression model.