Table 4. Somatic mutations in each subtype.
Somatic mutations | EBV (N=7) | MSI (N=19) | CIN (N=46) | GS (N=35) | P value | ||||
---|---|---|---|---|---|---|---|---|---|
Cases | (%) | Cases | (%) | Cases | (%) | Cases | (%) | ||
TP53 | 0 | 0.0% | 5 | 26.3% | 26 | 56.5% | 10 | 28.6% | 0.003a |
ACVR1B | 0 | 0.0% | 1 | 5.3% | 1 | 2.2% | 0 | 0.0% | 0.534 |
ALK | 0 | 0.0% | 3 | 15.8% | 2 | 4.3% | 1 | 2.9% | 0.232 |
APC | 2 | 28.6% | 1 | 5.3% | 8 | 17.4% | 1 | 2.9% | 0.050 |
ARID1A | 4 | 57.1% | 14 | 73.7% | 12 | 26.1% | 9 | 25.7% | 0.000a |
BCOR | 1 | 14.3% | 9 | 47.4% | 2 | 4.3% | 0 | 0.0% | 0.016a |
BRAF | 0 | 0.0% | 3 | 15.8% | 0 | 0.0% | 0 | 0.0% | 0.003a |
CBWD1 | 0 | 0.0% | 0 | 0.0% | 1 | 2.2% | 1 | 2.9% | 1.000 |
CCND1 | 0 | 0.0% | 3 | 15.8% | 2 | 4.3% | 2 | 5.7% | 0.323 |
CD274 | 1 | 14.3% | 0 | 0.0% | 0 | 0.0% | 0 | 0.0% | 0.065 |
CDH1 | 3 | 42.9% | 1 | 5.3% | 3 | 6.5% | 4 | 11.4% | 0.052 |
CIC | 0 | 0.0% | 5 | 26.3% | 3 | 6.5% | 2 | 5.7% | 0.082 |
CR1 | 0 | 0.0% | 5 | 26.3% | 2 | 4.3% | 8 | 22.9% | 0.220 |
CTNNB1 | 1 | 14.3% | 2 | 10.5% | 0 | 0.0% | 2 | 5.7% | 0.054 |
EGFR | 0 | 0.0% | 4 | 21.1% | 0 | 0.0% | 1 | 2.9% | 0.005a |
ERBB2 | 0 | 0.0% | 5 | 26.3% | 2 | 4.3% | 1 | 2.9% | 0.028a |
ERBB3 | 0 | 0.0% | 5 | 26.3% | 2 | 4.3% | 2 | 5.7% | 0.049a |
FBXW7 | 0 | 0.0% | 3 | 15.8% | 3 | 6.5% | 1 | 2.9% | 0.301 |
FGFR2 | 0 | 0.0% | 2 | 10.5% | 0 | 0.0% | 0 | 0.0% | 0.057 |
HLA-B | 0 | 0.0% | 3 | 15.8% | 2 | 4.3% | 0 | 0.0% | 0.088 |
IRF2 | 0 | 0.0% | 2 | 10.5% | 1 | 2.2% | 1 | 2.9% | 0.429 |
JAK2 | 0 | 0.0% | 1 | 5.3% | 1 | 2.2% | 0 | 0.0% | 0.534 |
KDR | 0 | 0.0% | 3 | 15.8% | 1 | 2.2% | 0 | 0.0% | 0.046a |
KRAS | 0 | 0.0% | 5 | 26.3% | 1 | 2.2% | 0 | 0.0% | 0.002a |
LARP4B | 0 | 0.0% | 3 | 15.8% | 1 | 2.2% | 0 | 0.0% | 0.046a |
MDM2 | 0 | 0.0% | 1 | 5.3% | 0 | 0.0% | 0 | 0.0% | 0.243 |
MEDAG | 0 | 0.0% | 2 | 10.5% | 0 | 0.0% | 0 | 0.0% | 0.057 |
MLH1 | 0 | 0.0% | 2 | 10.5% | 0 | 0.0% | 0 | 0.0% | 0.057 |
MSH2 | 0 | 0.0% | 4 | 21.1% | 1 | 2.2% | 0 | 0.0% | 0.009a |
MTOR | 0 | 0.0% | 3 | 15.8% | 3 | 6.5% | 0 | 0.0% | 0.111 |
MVK | 0 | 0.0% | 4 | 21.1% | 0 | 0.0% | 0 | 0.0% | 0.002a |
MYC | 1 | 14.3% | 0 | 0.0% | 0 | 0.0% | 0 | 0.0% | 0.065 |
PGM5 | 1 | 14.3% | 4 | 21.1% | 0 | 0.0% | 0 | 0.0% | 0.001a |
PIK3CA | 2 | 28.6% | 7 | 36.8% | 1 | 2.2% | 0 | 0.0% | 0.000a |
PTEN | 0 | 0.0% | 2 | 10.5% | 0 | 0.0% | 1 | 2.9% | 0.096 |
RHOA | 2 | 28.6% | 1 | 5.3% | 2 | 4.3% | 4 | 11.4% | 0.139 |
SMAD4 | 0 | 0.0% | 1 | 5.3% | 1 | 2.2% | 0 | 0.0% | 0.534 |
STK11 | 0 | 0.0% | 1 | 5.3% | 1 | 2.2% | 0 | 0.0% | 0.534 |
ZBTB20 | 0 | 0.0% | 5 | 26.3% | 0 | 0.0% | 0 | 0.0% | 0.000a |
Mutation rate | 2.6 | 6.6 | 1.8 | 1.5 |
ap value less than 0.05.
Abbreviations: CIN, chromosomal instability, EBV, Epstein-Barr virus; GS, genomically stable; MSI, microsatellite instability. Fisher`s exact test was performed to evaluate differences in the respective proportions of somatic mutations between subgroups.