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http://purl.uniprot.org/citations/31048362http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31048362http://www.w3.org/2000/01/rdf-schema#comment"Protein tyrosine phosphatase 1B (PTP1B) has been reported as an oncogene in hepatocellular carcinoma (HCC). However, how PTP1B is regulated in HCC remains unclear. MicroRNAs (miRNAs) are a class of small non-coding RNAs involved many biological processes including tumorigenesis. In this study, we investigated whether miRNA participated in the regulation of PTP1B in HCC. We found that miR-206, which was down-regulated during tumorigenesis, inhibited HCC cell proliferation and invasion. Overexpression of miR-206 inhibited proliferation, invasion, and migration of HCC cell lines HepG2 and Huh7. Mechanistically, we demonstrated that miR-206 directly targeted PTP1B by binding to the 3'-UTR of PTP1B mRNA as demonstrated by the luciferase reporter assay. Overexpression miR-206 inhibited PTP1B expression while miR-206 inhibition enhanced PTP1B expression in HepG2 and Huh7 cells. Functionally, the regulatory effect on cell proliferation/migration/invasion of miR-206 was reversed by PTP1B overexpression. Furthermore, tumor inoculation nude mice model was used to explore the function of miR-206 in vivo Our results showed that overexpression of miR-206 drastically inhibited tumor development. In summary, our data suggest that miR-206 inhibits HCC development by targeting PTP1B."xsd:string
http://purl.uniprot.org/citations/31048362http://purl.org/dc/terms/identifier"doi:10.1042/bsr20181823"xsd:string
http://purl.uniprot.org/citations/31048362http://purl.uniprot.org/core/author"Li X."xsd:string
http://purl.uniprot.org/citations/31048362http://purl.uniprot.org/core/author"Yang Q."xsd:string
http://purl.uniprot.org/citations/31048362http://purl.uniprot.org/core/author"Zhong Y."xsd:string
http://purl.uniprot.org/citations/31048362http://purl.uniprot.org/core/author"Zhang L."xsd:string
http://purl.uniprot.org/citations/31048362http://purl.uniprot.org/core/author"Lai L."xsd:string
http://purl.uniprot.org/citations/31048362http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/31048362http://purl.uniprot.org/core/name"Biosci Rep"xsd:string
http://purl.uniprot.org/citations/31048362http://purl.uniprot.org/core/pages"BSR20181823"xsd:string
http://purl.uniprot.org/citations/31048362http://purl.uniprot.org/core/title"miR-206 inhibits cell proliferation, invasion, and migration by down-regulating PTP1B in hepatocellular carcinoma."xsd:string
http://purl.uniprot.org/citations/31048362http://purl.uniprot.org/core/volume"39"xsd:string
http://purl.uniprot.org/citations/31048362http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/31048362
http://purl.uniprot.org/citations/31048362http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/31048362
http://purl.uniprot.org/uniprot/#_A8K3M3-mappedCitation-31048362http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31048362
http://purl.uniprot.org/uniprot/#_B4DSN5-mappedCitation-31048362http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31048362
http://purl.uniprot.org/uniprot/#_P18031-mappedCitation-31048362http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31048362
http://purl.uniprot.org/uniprot/#_Q96QT9-mappedCitation-31048362http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31048362
http://purl.uniprot.org/uniprot/Q96QT9http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/31048362
http://purl.uniprot.org/uniprot/A8K3M3http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/31048362
http://purl.uniprot.org/uniprot/P18031http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/31048362
http://purl.uniprot.org/uniprot/B4DSN5http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/31048362