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. 2020 Oct 2;11:540186. doi: 10.3389/fgene.2020.540186

TABLE 2.

Clinical and molecular characteristics of TCGA HCC patients according to the mutation/CNV status of m6A regulatory genes.

With mutation and/or CNV Without mutation or CNV P-value
Age ≤60 65 110 0.8699
>60 69 121
Gender male 106 142 0.0005
female 28 89
Histological grade G1 13 37 0.3807
G2 66 111
G3 48 72
G4 5 8
Pathological stage I 66 106 0.4808
II 35 50
III 24 56
IV 2 3
T stage T1 69 113 0.6385
T2 36 57
T3 24 51
T4 3 9
Tx 1 0
N stage N0 93 158 0.3010
N1 0 3
Nx 40 70
M stage M0 98 165 0.5584
M1 2 1
Mx 34 65
TP53 alteration 55 65 0.0114
wt 79 166

With mutation and/or CNV: cases have mutation or CNV or mutation + CNV. Without mutation or CNV: cases with neither mutation nor CNV. Ambiguous variables (Tx, Nx, and Mx) were excluded from chi-square test or Fisher’s exact test. Significant P values are in bold.