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mechanism remains unclear. SIRT1 is a class III histone/protein deacetylase (HDAC) and a member of the silent information regulator (Sir2) family. The mammalian sirtuin SIRT1 has received much attention for the roles it plays in regulating metabolism and
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on a HFD ( Arkan et al . 2005 , Solinas et al . 2007 ). SIRT1, an NAD + -dependent histone deacetylase, is an important regulator of the metabolic response to caloric restriction ( Chalkiadaki & Guarente 2012 ). Additional evidence indicates that
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Cancer Center, Departments of Medicine, Biochemistry, Pediatrics, Microbiology, Pathology and Laboratory Medicine, Boston University School of Medicine, 72 East Concord Street, Room K-701, Boston, Massachusetts 02118-2307, USA
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Introduction The sirtuins are a family of enzymes with increasingly recognized relevance to cancer ( Moore 2011 ), but the full extent of their involvement in breast cancer genesis and evolution remains to be elucidated. Sirtuin 1 (SIRT1) is a NAD
The ‘973’ National Basic Research Program of China, Changchun University of Chinese Medicine, Changchun, Jilin, People’s Republic of China
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) ( Giovannini et al . 2016 , Meek & Morton 2016 ), it is of great importance and urgency to develop more effective approaches to prevent the pathogenesis of diabetic vasculopathy. Previous reports highlighted the beneficial effect of sirtuin 1 (SIRT1
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between excess fructose consumption and impaired glucose and lipid homeostasis, the mechanisms responsible have yet to be elucidated. Recent studies have demonstrated the essential role of SIRT1, an NAD + -dependent protein deacetylase, in the regulation
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( Vanderford et al . 2007 ). SIRT1 is a deacetylase enzyme mostly located in the nucleus but also found in the cytoplasm under certain conditions ( Tanno et al . 2007 ). Its NAD-dependent activity suggests that this protein may sense the metabolic state of
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et al . 2003 , Rhee et al . 2003 ). SIRT1, an NAD + -dependent protein deacetylase, inhibits gluconeogenesis through disruption of TORC2 signalling. During fasting TORC2 is acetylated, which protects it against COP1-mediated ubiquitination and
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SIRT1, one of the seven members of the mammalian sirtuin family, has recently emerged. SIRT1 is known to regulate oocyte and somatic cell physiology during almost all stages of folliculogenesis ( Tatone et al. 2015 , 2018 ). Recently, our research
Department of Obstetrics and Gynaecology, Mercy Perinatal Research Centre, Department of Medicine, Mercy Hospital for Women, University of Melbourne, Level 4/163 Studley Road, Heidelberg 3084, Victoria, Australia
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Department of Obstetrics and Gynaecology, Mercy Perinatal Research Centre, Department of Medicine, Mercy Hospital for Women, University of Melbourne, Level 4/163 Studley Road, Heidelberg 3084, Victoria, Australia
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), IRS1 (QT00074144), PI3K p85α (QT01005984), GLUT1 (QT00068957), GLUT3 (QT00047124), GLUT4 (QT00097902) and SIRT1 (QT00051261) were purchased from Qiagen. The syncytin primer has previously been described ( Paiva et al . 2011 ). Average gene C T values
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Cancer Center, Medicine, Biochemistry, Pediatrics, Microbiology, Pathology and Laboratory Medicine, Departments of
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Cancer Center, Medicine, Biochemistry, Pediatrics, Microbiology, Pathology and Laboratory Medicine, Departments of
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other sirtuins in addition to Sir2p, whereas seven homologs have been identified in mammals, SIRT1–7 ( Frye 1999 , 2000 , Ford et al . 2005 , Yamamoto et al . 2007 ). Sirtuin activities are not limited to histone deacetylation; SIRT members can also