IndraLab

Statements


USP28 activates MYC. 26 / 26
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"USP28 has also been reported to antagonize ubiquitin-dependent degradation of the oncogene product MYC as well as JUN and Notch ."

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"FBXW7-185aa reduced the half-life of c-Myc by antagonizing USP28 induced c-Myc stabilization."

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"This peptide supposes to repress glioma malignancy through USP28 induced c-Myc stabilization."

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"Circ-FBXW7, highly expressed in normal human brain, has been reported to encode a novel 21-kDa protein, named FBXW7-185aa, that reduces the half-life of c-Myc by antagonizing USP28-induced c-Myc stabilization, thus acting as tumor suppressor in glioblastoma cells (34)."

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"Since FBW7gamma lacks the USP28 interaction motif of FBW7alpha, Usp28 selectively antagonize nucleoplasmic MYC degradation while not affecting nucleolar degradation."

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"In a previous study, circFBXW7 was found to be downregulated in glioma, where it is translated into a 185-amino acid (aa) protein (FBXW7-185aa) that competitively interacts with the deubiquitinating enzyme USP28, preventing USP28 from binding to FBXW7 and antagonizing USP28 induced c-Myc stabilization."

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"FBXW7-185aa reduced the half-life of c-Myc by antagonizing USP28-induced c-Myc stabilization."

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"A study by Zhang et al demonstrated that circ-FBXW7 encodes FBXW7-185aa, a protein consisting of 185 amino acids that can significantly inhibit tumour cell processes in vivo and reduce the half-life of c-Myc by antagonizing the stabilization effect of c-Myc induced by USP28."

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"Here, using murine genetic models, we determined that USP28 antagonizes the ubiquitin dependent degradation of c-MYC, a known USP28 substrate, as well as 2 additional oncogenic factors, c-JUN and NOTCH1, in the intestine."

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"Upregulation of FBXW7-185aa inhibited proliferation and cell cycle progression and reduced the half-life of c-Myc by antagonizing USP28 induced c-Myc stabilization in glioblastoma, while knockdown of FBXW7-185aa promoted malignant phenotypes in vitro and in vivo [XREF_BIBR]."
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"Usp28, an ubiquitin-specific protease, binds to myc through an interaction with fbw7alpha, an f-box protein that is part of an scf-type ubiquitin ligase. Therefore, it stabilizes myc."

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"The protein FBXW7-185aa functions as a tumor suppressor by competitively binding with USP28, and preventing USP28 binding to FBXW7α, subsequently inhibiting USP28-induced c-myc stabilization."

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"Independently, USP28 has been reported to modulate the activity of the Myc proto-oncogene [XREF_BIBR]."

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"A previous study in glioma implicated that the short protein FBXW7-185aa interacts with the deubiquitinating enzyme USP28, preventing USP28 from binding to FBXW7 and antagonizing USP28 induced c-Myc stabilization [XREF_BIBR]."

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"Knockdown of Usp28 results in a decrease of c-MYC while overexpression of the enzyme and leads to stabilization of the transcription factor ."

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"Besides, knockdown of USP28 blocked the effect of c-Myc on activation of ataxia telangiectasia-mutated and ataxia telangiectasia and Rad3 related DNA damage checkpoint after irradiation."

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"In this study FBXW7-185aa reduced the half-life of c-Myc by antagonizing USP28 induced c-Myc stabilization."

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"USP28 has also been reported to antagonize ubiquitin-dependent degradation of the oncogene product MYC as well as JUN and Notch 105 ."

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"Independently, USP28 has been reported to modulate the activity of the Myc proto-oncogene [126]."

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"Additionally, a deubiquitinase, USP28, has been reported to antagonize ubiquitin dependent proteasomal degradation of c-Myc."

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"In one study, FBXW7-185aa reduced the half-life of c-Myc by antagonizing USP28 induced c-Myc stabilization 43."

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"Interestingly, Yang et al. [75] identified a circular RNA encoding circ-FBXW7, whose expression in GBM samples was lower compared to the surrounding normal tissue, being capable of antagonizing the stabilization of the oncoprotein c-MYC initiated by the deubiquitinase USP28; circ-FBXW7 expression was linked to greater survival in patients."

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"USP28 can counteract the activity of FBW7 and promote c-MYC stability in cancer cells."

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"The FBXW7-185aa protein can reduce the half-life of the c-Myc oncoprotein, which is known to regulate the transcription of numerous genes and pathways, via antagonizing ubiquitin carboxyl-terminal hydrolase 28 (USP28) induced c-Myc stabilization in glioma cells (Yang et al., 2018)."

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"Therefore, FBXW-185aa prevents FBXW7alpha induced degradation by antagonizing USP28 induced c-Myc stabilization."

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"55 Usp28 mediated Myc stabilization is required for tumor cell proliferation and has shown clinical significance in non small cell lung cancer, breast cancer, intestinal cancer, gliomas, and bladder cancer."