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http://purl.uniprot.org/citations/28579116http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28579116http://www.w3.org/2000/01/rdf-schema#comment"Silent mating type information regulation 2 homolog 3 (SIRT3) is a major protective mediator that ameliorates oxidative stress and mitochondrial dysfunction, which are associated with the pathogenesis of epithelial-mesenchymal transition (EMT). The present study was aimed to investigate the potential role of SIRT3 in renal tubular EMT both in vitro and in vivo. Firstly, we showed that the expression of SIRT3 was repressed in angiotensin II-induced EMT. SIRT3 deficiency triggered EMT response, while over-expression of SIRT3 attenuated EMT response. In addition, over-expression of SIRT3 repressed AngⅡ-induced excessive production of mitochondrial superoxide, as well as mitochondrial dysfunction evidenced by the maintenance of mitochondrial number and morphology, and the stabilization of mitochondrial membrane potential. In conclusion, these findings identify a protective role of SIRT3 against angiotensin II-induced EMT in the kidney, and suggest SIRT3 upregulation is a potential therapeutic strategy for the treatment of renal tubulointerstitial fibrosis."xsd:string
http://purl.uniprot.org/citations/28579116http://purl.org/dc/terms/identifier"doi:10.1016/j.mce.2017.04.027"xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/author"Chen S."xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/author"Feng G."xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/author"Huang Y."xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/author"Gao H."xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/author"Li Z."xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/author"Liu P."xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/author"Wang P."xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/author"Hong H."xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/author"He P."xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/author"Luo W."xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/author"Liang L."xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/author"Yue Z."xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/date"2018"xsd:gYear
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/name"Mol Cell Endocrinol"xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/pages"1-13"xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/title"SIRT3 prevents angiotensin II-induced renal tubular epithelial-mesenchymal transition by ameliorating oxidative stress and mitochondrial dysfunction."xsd:string
http://purl.uniprot.org/citations/28579116http://purl.uniprot.org/core/volume"460"xsd:string
http://purl.uniprot.org/citations/28579116http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/28579116
http://purl.uniprot.org/citations/28579116http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/28579116
http://purl.uniprot.org/uniprot/#_D3YVQ5-mappedCitation-28579116http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28579116
http://purl.uniprot.org/uniprot/#_D3YWD6-mappedCitation-28579116http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28579116
http://purl.uniprot.org/uniprot/#_A0A1B0GRF7-mappedCitation-28579116http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28579116