Corrigendum: PKM2-Induced the Phosphorylation of Histone H3 Contributes to EGF-Mediated PD-L1 Transcription in HCC

In the original article, there were several errors in Figures and Figure legends. In Figure 2 as published, the letters of B and C which indicated the figure order were marked reverse. In Figure 4, the letters of B to E which indicated the figure order were marked reverse, and figure label "EGF" was missed in the second and third bands in Western blots in Figure 4B. In Figure 6B Lamin B1 was used as internal control and β-actin was used as negative control. **p < 0.01, a two-tailed unpaired t-test, n = 8 rats per group. (D) The phosphorylational level of H3-Thr 11 was increased in the livers of DEN-treated rats. **p < 0.01, a two-tailed unpaired t-test, n = 8 rats per group (E and F) The expression of PD-L1 mRNA (E) and protein (F) was increased in the livers of DEN-treated rats. **p < 0.01, ***p < 0.001, a two-tailed unpaired t-test, n =8 rats per group. (G) ChIP analyses showed that DEN administration resulted in enhanced H3-Thr 11 phosphorylation at the PD-L1 promoter in rats. **p < 0.01, a two-tailed unpaired t-test, n =8 per group.

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