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http://purl.uniprot.org/citations/33461373http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/33461373http://www.w3.org/2000/01/rdf-schema#comment"Triple-negative breast cancer (TNBC) is the most aggressive histological subtype of breast cancer and is characterized by poor outcomes and a lack of specific-targeted therapies. Transforming growth factor-β (TGF-β) acts as the key cytokine in the epithelial-mesenchymal transition (EMT) and the metastasis of TNBC. However, the regulatory mechanisms of the TGF-β signaling pathway remain largely unknown. In this study, we identified that the USP1/WDR48 complex could effectively enhance TGF-β-mediated EMT and migration of TNBC cells. Furthermore, lower phosphorylation of Smad2/3, Erk, Jnk, and p38 was noted on the suppression of the expression of endogenous USP1 or WDR48. Moreover, the USP1-WDR48 complex was found to downregulate the polyubiquitination of TAK1 and mediate its in vitro stability. Therefore, our findings have shed a light on the novel role of the USP1/WDR48 complex in promoting TGF-β-induced EMT and migration in TNBC via in vitro stabilization of TAK1."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.org/dc/terms/identifier"doi:10.1080/15384101.2021.1874695"xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Chen B."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Chen T."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Han D."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Li C."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Liu Y."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Li Z."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Li Y."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Liang Y."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Luo D."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Song X."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Yang Q."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Zhang H."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Wang L."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Wang X."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/author"Zhao W."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/name"Cell Cycle"xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/pages"320-331"xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/title"USP1-WDR48 deubiquitinase complex enhances TGF-beta induced epithelial-mesenchymal transition of TNBC cells via stabilizing TAK1."xsd:string
http://purl.uniprot.org/citations/33461373http://purl.uniprot.org/core/volume"20"xsd:string
http://purl.uniprot.org/citations/33461373http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/33461373
http://purl.uniprot.org/citations/33461373http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/33461373