IndraLab

Statements


USP24 activates HYCC1. 11 / 11
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"Taken together, USP24 can be employed as a promising target to restrain tumor growth and increase the efficacy of HCC immunotherapy."

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"The results indicated that USP24 overexpression decreased wound-healing ability (Fig. 5F and Supplementary Fig. 3A, B) and inhibited the migration of HCC cells (Fig. 5G, H)."

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"Depletion of USP24 significantly suppressed the proliferation of HCC cells in vitro, which could be rescued by restoration of YAP1."

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"Knocking down USP24 promotes HCC proliferation and migration, whereas USP24 overexpression inhibits HCC in vitro and in vivo."

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"We find that increased autophagy is accompanied by ferroptosis in USP24 overexpressed HCC cells and USP24 increases the susceptibility of HCC to sorafenib."

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"These results suggested that USP24 promotes ferroptosis of HCC cells.Taking into account that ferroptosis is a type of autophagic cell death, which we called ferritinophagy , the Fe level was measured using a colorimetric assay and a fluorescence probe."

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"Altogether, these results demonstrate that USP24 levels are significantly elevated in HCC and that its expression also plays an important role in predicting the clinical outcomes of patients with HCC."

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"The results indicated that overexpression of USP24 decreased GSH while increased the level of MDA in HCC cells (Fig. 7H, I and Supplementary Fig. 4G, H), further confirming that USP24 promotes ferroptosis in HCC cells."

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"To investigate whether USP24 knockdown suppressed the tumorigenesis of HCC cells in vivo, we injected Bel-7402 cells which were stably knockdown USP24 (shUSP24-2) or the negative control (shNC) into the subcutaneous of the nude mice."

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"USP24 markedly promoted HCC proliferation and progression in vitro and in vivo."

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"In addition, we also found that USP24 promoted cell proliferation and tumor growth of HCC in vitro and in vivo."