2020
DOI: 10.3390/cells9030702
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Tissue-Specific Metabolic Regulation of FOXO-Binding Protein: FOXO Does Not Act Alone

Abstract: The transcription factor forkhead box (FOXO) controls important biological responses, including proliferation, apoptosis, differentiation, metabolism, and oxidative stress resistance. The transcriptional activity of FOXO is tightly regulated in a variety of cellular processes. FOXO can convert the external stimuli of insulin, growth factors, nutrients, cytokines, and oxidative stress into cell-specific biological responses by regulating the transcriptional activity of target genes. However, how a single transc… Show more

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Cited by 40 publications
(32 citation statements)
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“…FoxO transcription factors usually activate or suppress gene expression via direct binding to DNA target sites and interaction with other effectors [ 36 , 37 ]. Both in vitro and in vivo assays strongly indicate that Nl FoxO showed strongest binding capacity to FRE1 located in the first intron region of the Nlvg locus.…”
Section: Discussionmentioning
confidence: 99%
“…FoxO transcription factors usually activate or suppress gene expression via direct binding to DNA target sites and interaction with other effectors [ 36 , 37 ]. Both in vitro and in vivo assays strongly indicate that Nl FoxO showed strongest binding capacity to FRE1 located in the first intron region of the Nlvg locus.…”
Section: Discussionmentioning
confidence: 99%
“…But, in addition to site‐of‐expression, physiological context is crucial in determining whether a protein has beneficial, benign, or detrimental impacts. A regulatory factor may act in different tissues to modulate different biological processes (Kodani & Nakae, 2020). Or, within the same tissue, the activity of a protein may have diametrically opposite effects on different aspects of health (Amrit et al, 2019).…”
Section: Discussionmentioning
confidence: 99%
“…Similarly, HG-mediated elevation of miR-199a-5p was suggested to be a culprit of SIRT1 reduction along with apoptosis and ROS generation in pancreatic β-cells [191]. Far less studied molecule from sirtuins family, SIRT3, positively regulates FOXO1/3, thus resulting in antioxidative response [192,193]. Expression level of SIRT3 was declined due to upregulation of miR-7977 upon hyperinsulinemia in tubular epithelial cells, while contributing to promotion of OxS [194].…”
Section: Mirnas In Mets-a Link With Obesity and Insulin Resistance/hymentioning
confidence: 99%