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USP47 activates SATB1. 8 / 8
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"The deficiency of USP47 impaired the transcriptional activity of SATB1 target genes and inhibited cell proliferation, migration, and tumorigenesis in a mouse model of colon cancer."

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"These results suggested that USP47 could mediate EMT by stabilizing SATB1 (Yu et al., 2019)."

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"USP47 deficiency impairs transcriptional activity of SATB1 target genes and inhibits proliferation, migration, and tumorigenesis (68, 69)."

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"As shown in Fig. 2 G and H, and S3B , the catalytically inactive USP47/CS mutant failed to protect SATB1 from degradation, implying that deubiquitinase activity is required for USP47-mediated SATB1 st[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

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"Likewise, knockdown of USP47 in HCT116 cells promoted SATB1 degradation ( Fig. S3C )."

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"In addition, we determined whether USP47-mediated SATB1 stability is achieved via proteasomes."

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"As seen from Fig. 2 I, MG132 (proteasome inhibitor) treatment could rescue the USP47 knockout-mediated degradation of the SATB1 protein."

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"We also provided evidence that USP47 positively regulated SATB1 stability."