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http://purl.uniprot.org/citations/25060766http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/25060766http://www.w3.org/2000/01/rdf-schema#comment"MicroRNAs (miRNAs) have recently been recognized to have a role in human orthopedic disorders. The objective of our study was to explore the expression profile and biological function of miRNA-17-5p (miR-17-5p), which is well known to be related to cancer cell proliferation and invasion, in osteoblastic differentiation and in cell proliferation. The expression levels of miR-17-5p in the femoral head mesenchymal stem cells of 20 patients with non-traumatic osteonecrosis (ON) and 10 patients with osteoarthritis (OA) were examined by quantitative reverse transcription-PCR (qRT-PCR). Furthermore, the interaction between miR-17-5p and SMAD7 was observed. We found that in non-traumatic ON samples the level of mature miR-17-5p was significantly lower than that of OA samples (P=0.0002). By targeting SMAD7, miR-17-5p promoted nuclear translocation of β-catenin, enhanced expression of COL1A1 and finally facilitated the proliferation and differentiation of HMSC-bm cells. We also demonstrated that restoring expression of SMAD7 in HMSC-bm cells partially reversed the function of miR-17-5p. Together, our data suggested a theory that dysfunction of a network containing miR-17-5p, SMAD7 and β-catenin could contribute to ON pathogenesis. The present study prompts the potential clinical value of miR-17-5p in non-traumatic ON."xsd:string
http://purl.uniprot.org/citations/25060766http://purl.org/dc/terms/identifier"doi:10.1038/emm.2014.43"xsd:string
http://purl.uniprot.org/citations/25060766http://purl.uniprot.org/core/author"Feng Y."xsd:string
http://purl.uniprot.org/citations/25060766http://purl.uniprot.org/core/author"Jia J."xsd:string
http://purl.uniprot.org/citations/25060766http://purl.uniprot.org/core/author"Feng X."xsd:string
http://purl.uniprot.org/citations/25060766http://purl.uniprot.org/core/author"Liu X."xsd:string
http://purl.uniprot.org/citations/25060766http://purl.uniprot.org/core/author"Xu W."xsd:string
http://purl.uniprot.org/citations/25060766http://purl.uniprot.org/core/author"Zhang Q."xsd:string
http://purl.uniprot.org/citations/25060766http://purl.uniprot.org/core/author"Yang S."xsd:string
http://purl.uniprot.org/citations/25060766http://purl.uniprot.org/core/author"Dai Z."xsd:string
http://purl.uniprot.org/citations/25060766http://purl.uniprot.org/core/date"2014"xsd:gYear
http://purl.uniprot.org/citations/25060766http://purl.uniprot.org/core/name"Exp Mol Med"xsd:string
http://purl.uniprot.org/citations/25060766http://purl.uniprot.org/core/pages"e107"xsd:string
http://purl.uniprot.org/citations/25060766http://purl.uniprot.org/core/title"MiR-17-5p modulates osteoblastic differentiation and cell proliferation by targeting SMAD7 in non-traumatic osteonecrosis."xsd:string
http://purl.uniprot.org/citations/25060766http://purl.uniprot.org/core/volume"46"xsd:string
http://purl.uniprot.org/citations/25060766http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/25060766
http://purl.uniprot.org/citations/25060766http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/25060766
http://purl.uniprot.org/uniprot/#_B3KYA8-mappedCitation-25060766http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/25060766
http://purl.uniprot.org/uniprot/#_O15105-mappedCitation-25060766http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/25060766
http://purl.uniprot.org/uniprot/B3KYA8http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/25060766
http://purl.uniprot.org/uniprot/O15105http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/25060766