However, it is notable that among the candidates that potentially bind to MNSFβ, ribosomal protein S3A (RPS3A) was reported to promote the biological processes related to tumourigenesis, metastasis and immunosuppression in hepatocellular carcinoma patients,31 human zinc finger RNA‐binding protein (ZFR) repressed the interferon response by preventing aberrant splicing and nonsense‐mediated decay of histone variant macroH2A1/H2AFY mRNAs to regulate macrophage differentiation.32 Here, MACROH2A1 is linked to hepatocellular carcinoma.