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. 2020 May 6;69(9):1891–1903. doi: 10.1007/s00262-020-02586-9

Table 1.

IRF-1, IRF-2, and PD-L1 mRNA in relationship with clinical characteristics of 31 HCC patients included in this study

Variable IRF-1 IRF-2 PD-L1
N Mean ± SEM p Mean ± SEM p Mean ± SEM p
Age
  ≤ 71 17 1.48 ± 0.41 0.106 1.52 ± 0.31 0.105 0.59 ± 0.16 0.329
  > 71 14 0.67 ± 0.14 0.90 ± 0.15 0.40 ± 0.07
Sex
 Male 23 1.23 ± 0.32 0.403 1.32 ± 0.24 0.481 0.52 ± 0.13 0.702
 Female 8 0.76 ± 0.24 1.01 ± 0.23 0.44 ± 0.10
HBs Ag
  +  4 0.70 ± 0.33 0.531 1.42 ± 0.53 0.719 0.61 ± 0.35 0.667
 − 27 1.17 ± 0.27 1.21 ± 0.20 0.48 ± 0.10
HCV Ab
  +  7 1.45 ± 0.49 0.462 1.06 ± 0.13 0.617 0.50 ± 0.25 0.9886
 − 24 1.01 ± 0.28 1.29 ± 0.24 0.50 ± 0.10
Differentiation
 Well 6 2.31 ± 0.95 0.037* 1.91 ± 0.83 0.218 0.76 ± 0.31 0.269
 Moderate 22 0.84 ± 0.18 1.09 ± 0.13 0.46 ± 0.10
 Poor 3 0.55 ± 0.03 1.07 ± 0.13 0.18 ± 0.07
TNM stage
 I 8 2.49 ± 0.72 0.004** 1.73 ± 0.62 0.514 0.75 ± 0.21 0.159
 II 13 0.54 ± 0.10 1.10 ± 0.18 0.38 ± 0.12
 IIIA 6 0.58 ± 0.23 1.01 ± 0.30 0.37 ± 0.11
 IIIB 4 1.01 ± 0.30 1.07 ± 0.27 0.22 ± 0.07

Bold indicates *p < 0.05, **p < 0.01

HBs Ag, hepatitis; B, surface antigen; HCV Ab, hepatitis C virus antibody; TNM, Tumor Node Metastasis