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. 2014 May 12;9(5):e96958. doi: 10.1371/journal.pone.0096958

Table 3. Logistic regression analyses of associations between p21, p53, TP53BP1 and p73 polymorphisms and risk of ESCC.

Genotype Cases (n = 629) Controls (n = 686) Crude OR (95%CI) p Adjusted OR a (95%CI) p
n % n %
p21 rs2395655 G>A
GG 148 24.7 184 28.3 1.00 1.00
GA 327 54.5 318 48.8 1.28 (0.98–1.67) 0.070 1.23 (0.94–1.62) 0.128
AA 125 20.8 149 22.9 1.04 (0.76–1.44) 0.798 1.00 (0.72–1.39) 0.982
GA+AA 452 75.3 467 71.7 1.20 (0.94–1.55) 0.150 1.16 (0.90–1.50) 0.256
GG+GA 475 79.2 502 77.1 1.00 1.00
AA 125 20.8 149 22.9 0.89 (0.68–1.16) 0.381 0.87 (0.66–1.15) 0.332
p21 rs1059234 C>T
CC 172 28.7 170 26.1 1.00 1.00
CT 321 53.5 340 52.2 0.93 (0.72–1.21) 0.604 0.88 (0.67–1.15) 0.334
TT 107 17.8 141 21.7 0.75 (0.54–1.04) 0.086 0.72 (0.51–1.00) 0.050
CT+TT 428 71.3 481 73.9 0.88 (0.69–1.13) 0.311 0.83 (0.64–1.07) 0.149
CC+CT 493 82.2 510 78.3 1.00 1.00
TT 107 17.8 141 21.7 0.79 (0.59–1.04) 0.090 0.78 (0.59–1.04) 0.089
p21 rs3176352 G>C
GG 191 31.8 239 35.5 1.00 1.00
GC 258 43.0 316 47.0 1.02 (0.79–1.31) 0.868 0.98 (0.76–1.27) 0.866
CC 151 25.2 118 17.5 1.60 (1.182.18) 0.0026 1.61 (1.182.20) 0.0030
GC+CC 409 68.2 434 64.5 1.18 (0.93–1.49) 0.166 1.15 (0.91–1.46) 0.255
GG+GC 449 74.8 555 82.5 1.00 1.00
CC 151 25.2 118 17.5 1.58 (1.212.07) 0.0009 1.63 (1.232.15) 0.0006
p21 rs1801270 C>A
CC 179 29.1 182 26.7 1.00 1.00
CA 322 52.3 346 50.8 0.95 (0.73–1.22) 0.672 0.89 (0.68–1.15) 0.373
AA 115 18.7 153 22.5 0.76 (0.56–1.05) 0.097 0.72 (0.520.99) 0.044
CA+AA 437 70.9 499 73.3 0.89 (0.70–1.14) 0.349 0.84 (0.65–1.07) 0.154
CC+CA 501 81.3 528 77.5 1.00 1.00
AA 115 18.7 153 22.5 0.79 (0.60–1.04) 0.092 0.77 (0.59–1.02) 0.070
p21 rs762623 G>A
GG 480 77.9 537 78.9 1.00 1.00
GA 129 20.9 136 20.0 1.06 (0.81–1.39) 0.667 1.06 (0.81–1.40) 0.675
AA 7 1.1 8 1.2 0.98 (0.35–2.72) 0.967 0.95 (0.33–2.70) 0.923
GA+AA 136 22.1 144 21.1 1.06 (0.81–1.38) 0.683 1.06 (0.81–1.38) 0.700
GG+GA 609 98.9 673 98.8 1.00 1.00
AA 7 1.1 8 1.2 0.97 (0.35–2.68) 0.949 0.94 (0.33–2.67) 0.905
p53 rs1042522 G>C
GG 177 28.8 213 32.6 1.00 1.00
GC 321 52.3 310 47.5 1.25 (0.97–1.61) 0.089 1.19 (0.92–1.54) 0.186
CC 116 18.9 130 19.9 1.07 (0.78–1.48) 0.663 1.04 (0.75–1.44) 0.810
GC+CC 437 71.2 440 67.4 1.20 (0.94–1.52) 0.144 1.15 (0.90–1.46) 0.273
GG+GC 498 81.1 523 80.1 1.00 1.00
CC 116 18.9 130 19.9 0.94 (0.71–1.24) 0.648 0.93 (0.70–1.24) 0.639
TP53BP1 rs560191 G>C
GG 213 34.6 216 33.1 1.00 1.00
GC 291 47.3 290 44.4 1.02 (0.79–1.31) 0.891 1.01 (0.78–1.30) 0.959
CC 111 18.0 147 22.5 0.77 (0.56–1.05) 0.092 0.76 (0.56–1.05) 0.093
GC+CC 402 65.4 437 66.9 0.93 (0.74–1.18) 0.558 0.92 (0.73–1.17) 0.515
GG+GC 504 82.0 506 77.5 1.00 1.00
CC 111 18.0 147 22.5 0.76 (0.581.00) 0.049 0.76 (0.57–1.01) 0.055
p73 rs1801173 C>T
CC 311 51.8 401 59.6 1.00 1.00
CT 251 41.8 235 34.9 1.38 (1.091.74) 0.007 1.39 (1.101.76) 0.006
TT 38 6.3 37 5.5 1.32 (0.82–2.13) 0.248 1.27 (0.78–2.07) 0.337
CT+TT 289 48.2 272 40.4 1.37 (1.101.71) 0.006 1.37 (1.101.72) 0.006
CC+CT 562 93.7 636 94.5 1.00 1.00
TT 38 6.3 37 5.5 1.16 (0.73–1.85) 0.527 1.11 (0.69–1.79) 0.667
p21 rs3176352 G>C and p73 rs1801173 C>T combinations
No risk variant genotypeb 226 37.7 323 48.0 1.00 1.00
Either one risk variant genotype 308 51.3 310 46.1 1.42 (1.131.79) 0.0030 1.42 (1.121.80) 0.0035
Both risk variant genotypes 66 11.0 40 5.9 2.36 (1.543.62) <0.0001 2.47 (1.603.82) <0.0001
a

Adjusted for age, sex, smoking status and alcohol consumption;

b

Risk variant genotype means p21 rs3176352 CC or p73 rs1801173 CT/TT; p21 rs3176352 C vs. G OR = 1.26, 95% CI = 1.08–1.47, p = 0.0041; p73 rs1801173 T vs. C OR = 1.26, 95% CI = 1.05–1.50, p = 0.0126. Bonferroni correction (number of mutiple test = 32) was performed to correct the p value (p correct); for p21 rs3176352 G>C, the p correct = 0.096 for CC vs. GG after adjusted for age et al., p correct = 0.0192 for CC vs. GG/GC. For p73 rs1801173 C>T, the p correct = 0.202 for CT vs. CC after adjusted for age et al., p correct = 0.195 for CT/TT vs. CC. For the rest 6 SNPs, p correct>0.05 in all comparison models; Bold values are statistically significant (p<0.05).