IndraLab

Statements

USP13 deubiquitinates SNAI1. 5 / 5
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"Further evidence showed that EMT might be the primary mechanism for the enhanced metastatic property in GC cells: USP13 and USP29 promoted TGF-β1-induced EMT through interacting with and deubiquitinating Snail, while USP3 facilitated this process by deubiquitinating SUZ12 (Wu et al. 2021; Zhang et al. 2022a, b; Qian et al. 2020)."
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"The report from Zhang et al. revealed that USP13 promotes the epithelial-mesenchymal transition (EMT) and metastasis in GC by deubiquitinating and stabilizing Snail in GC [10]."
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"The transcriptional activator PLAGL2 activates the ubiquitin-specific peptidase 13 (USP13), which deubiquitinates and maintains Snail to influence the metastatic power of GC cells [64]."
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"USP13 interacted with Snail to deubiquitinate and stabilize Snail in GC cells."
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"USP13, USP29, and USP37 were reported to promote the metastasis of GC by deubiquitinating and stabilizing Snail [35,36,54,59]."
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