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. 2016 Sep 8;7(40):64910–64920. doi: 10.18632/oncotarget.11912

Table 1. Immunohistochemical expression characteristics of TP53 mutations.

Mutation features p53 immunohistochemistry p-valuea
Total (n = 7878) Negative (%) (n = 1852) Positive (%) (n = 6026)
Exons/introns
exons 7690 1745 (22.69) 5945 (77.31) 0.001
introns 186 105 (56.45) 2086 (43.55)
NA 2 2 (100.00) 0 (0.00)
CpG site
no 5373 1433 (26.67) 3940 (73.33) < 0.0001
yes 2505 419 (16.73) 2086 (83.27) < 0.0001
Splice site
alternative 71 12 (16.90) 59 (83.10) 0.1872
consensus 112 72 (64.29) 40 (35.71) < 0.0001
criptic 62 16 (25.81) 46 (74.19) 0.6684
no 7633 1752 (22.95) 5881 (77.05) < 0.0001
Type
Single nucleotide mutationsb 6860 1324 (19.30) 5536 (80.70) <0.0001
tandem 97 6 (6.19) 91 (93.81) 5.16E-05
complex 48 18 (37.50) 30 (72.50) 0.0219
deletion 667 380 (56.97) 287 (43.03) <0.0001
insertion 196 117 (59.69) 79 (40.31) <0.0001
NA 10 7 (70.00) 3 (30.00) 0.000522
Effects
frameshift 677 451 (66.62) 226 (33.38) <0.0001
intronic 53 25 (47.17) 28 (52.83) 4.58E-05
large deletion 2 2 (100.00) 0 (0.00) 0.0107
missense 5889 707 (12.01) 5182 (87.99) <0.0001
nonsense 552 393 (71.20) 159 (28.80) <0.0001
silent 367 136 (37.06) 231 (62.94) 3.64E-10
splice 131 86 (65.65) 45 (34.35) <0.0001
other 177 44 (24.86) 133 (75.14) 0.6683
NA 30 8 (26.67) 22 (73.33) 0.6828
Structural motif
C-terminal 234 104 (44.44) 130 (55.56) <0.0001
C- terminal/NLS 31 13 (41.94) 18 (58.06) 0.0153
C- terminal/tetramerization 101 39 (38.61) 62 (61.39) 3.15E-04
L1/S/H2 1693 234 (13.82) 1459 (86.18) <0.0001
L2/L3 2765 434 (15.70) 2331 (84.30) <0.0001
N- terminal 34 26 (76.47) 8 (23.53) <0.0001
N- terminal/Transactivation 33 20 (60.61) 13 (39.39) <0.0001
N- terminal/Transactivation/ NES 5 2 (40.00) 3 (60.00) 0.3844
NDBL/β-sheets 2657 795 (29.92) 1862 (70.08) <0.0001
SH3-like/Proline-rich 101 60 (59.41) 41 (40.59) <0.0001
NA 224 125 (55.80) 99 (44.20) <0.0001
a

Comparisons between groups were performed with Pearson's Chi-square (χ2), Significant p-values are marked in bold;

b

Containing the following point mutations: A:T>C:G, A:T>G:C, A:T>T:A, G:C>A:T, G:C>A:T at CpG, G:C>C:G and G:C>T:A)