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IL-1 ubiquitylation on lysine K133 promotes IL-1 turnover, and loss of IL-1 K133 ubiquitylation via the generation of Il1b K133R/K133R mice enhances i) pro-IL-1 protein levels, ii) the capacity of IL-1 to be activated following NLRP3 triggering, and iii) increases levels of precursor and activated IL-1 following LPS injection

This leads to an increased synthesis of GH, effectively expanding the pool of GH available for secretion within the somatotroph

Similar findings were also observed in rat hepatoma tissues [18] and human HCC tissue [19,20] as compared to non-HCC tissues

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