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ELAVL1 binds USP8. 14 / 14
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"Given our most recent studies indicating that HUR protein binds to USP8 mRNA and stabilizes USP8 mRNA [ xref ], and lncRNAs binds to their targeted protein and affects their bound protein function [ xref – xref ], we further probed the potential interaction between SNHG1 and HUR protein and the data obtained from the online analyses using catRAPID, RPISeq, StarBase V2.0 did suggest their interaction."
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"Further studies revealed that ChlA-F treatment induces HuR protein expression and that the increased HuR interacts with USP8 mRNA, resulting in elevation of USP8 mRNA stability and protein expression."
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"In non-small cell lung cancer, lncRNA SNHG12 bridges the interaction between USP8 mRNA and HuR, thereby enhancing the stability of HuR and achieving an increase in the expression of USP8 [ xref ]."
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"Based on the HUR interaction with USP8 mRNA or SNHG1 , we postulated that SNHG1 might serve as a competitive endogenous RNA for USP8 mRNA by binding with HUR protein."
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"Direct binding of SNHG12 to HuR, as well as binding of PD-L1 and USP8 to HuR, was predicted using RNA–protein interaction prediction (RPISeq) (http://pridb.gdcb.iastate.edu/RPISeq/, accessed on 19 June 2023) and validated by RIP assay [151]."
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"The database prediction indicated a comparatively high probability of HuR binding to USP8 (Fig.  xref A)."
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"RIP assay further verified that HuR could bind to USP8 mRNA in NSCLC cells ( P  < 0.01, Fig.  xref B)."
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"Additionally, ChlA-F induced the expression of HuR, which binds to USP8 mRNA and increases its stability."
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"Additionally, ChlA-F induced the expression of HuR, which binds to USP8 mRNA and increases its stability."
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"The scores of SNHG12 binding to HuR, and HuR binding to PD-L1 and USP8 were predicted using RNA–Protein Interaction Prediction (RPISeq) (http://pridb.gdcb.iastate.edu/RPISeq/) [29]."
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No evidence text available
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"The database prediction indicated a comparatively high probability of HuR binding to USP8 (Fig. 5A)."
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"This interaction reduced HUR binding to ubiquitin-specific peptidase 8 (USP8) mRNA, causing degradation of USP8 mRNA and a subsequent decrease in USP8 protein expression."
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"Based on the HUR interaction with USP8 mRNA or SNHG1, we postulated that SNHG1 might serve as a competitive endogenous RNA for USP8 mRNA by binding with HUR protein."
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