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the miRNA-223can maintain cell proliferation of breast cancer cell through targeting FOXO 1.
MEG3 (show FAM129B Proteins) acts as a ceRNA to regulate expression of E-cadherin (show CDH1 Proteins) and FOXO1 by competitively binding miR (show MLXIP Proteins)-9 and may be used as a potential biomarker in predicting ESCC patients' progression and prognosis
These results strongly suggest that AMPK (show PRKAA1 Proteins) can activate ORP150 (show HYOU1 Proteins) through FOXO1 pathway and confer protection against endoplasmic reticulum stress - induced apoptosis of airway epithelial cells following exposure to cigarette smoke extract.
LAT1 (show LAT Proteins)-NAD+-SIRT1 (show SIRT1 Proteins) signaling is activated in tumor tissues of patients with non-small cell lung cancer; NAD+ synthesis regulates the SIRT1 (show SIRT1 Proteins)-FOXO1 apoptotic pathway in response to NQO1 (show NQO1 Proteins)
Knockdown of FOXO4 (show FOXO4 Proteins) but not FOXO1 expression decreased proteasome activity. Following neural differentiation, the HD-iPSC-derived neural progenitor cells (NPCs) demonstrated lower levels of proteasome activity and FOXO (show FOXO3 Proteins) expressions than their WT counterparts. More importantly, overexpression of FOXO4 (show FOXO4 Proteins) but not FOXO1 in HD NPCs dramatically enhanced proteasome activity.
The borders of this novel topologically associating domains (TADs)correspond to the original 5'- and 3'- borders of the PAX3 (show PAX3 Proteins) and FOXO1 TADs, respectively, suggesting that TAD (show CRTAM Proteins) organisation precedes the formation of regulatory long-range interactions. Our results demonstrate that, upon translocation, novel regulatory landscapes are formed allowing new intra-TAD (show CRTAM Proteins) interactions between the original loci involved
In this study, the long noncoding RNA MALAT1, confirmed to be significantly upregulated in OS, is first shown to be capable of promoting proliferation and migration by directly suppressing miR (show MLXIP Proteins)-26a-5p in OS cells. Authors have identified forkhead box O1 (FOXO1) as a transcriptional factor of MALAT1 that can negatively regulate MALAT1.
miR (show MLXIP Proteins)-145 suppressed STAT3 (show STAT3 Proteins) phosphorylation at Tyr705 and increased foxo1 promoter transcriptional activity in T24 cells, but not in T24T cells, suggesting a role of STAT3 (show STAT3 Proteins) in the divergent responses to miR (show MLXIP Proteins)-145.
KLF4 (show KLF4 Proteins) transcriptionally repressed FOXO1 expression in glioma cells, contributing to glioma cell invasion and growth.
this study provides the first evidence that FOXO1 can reverse epithelial-to-mesenchymal transition in hepatocellular carcinoma via the transcription inducers Snail (show SNAI1 Proteins), Slug, ZEB1, ZEB2 and Twist1 (show TWIST1 Proteins), with ZEB2 playing a particularly critical role in this process. Furthermore, FOXO1 disrupts TGF-beta (show TGFB1 Proteins)-induced epithelial-to-mesenchymal transition.
These results indicate that miR (show MYLIP Proteins)-182 functions as a FoxO1 inhibitor to antagonize osteoblast proliferation and differentiation, with a subsequent negative effect on osteogenesis.
gas6 (show GAS6 Proteins) protects endothelial cells from apoptosis by a mechanism that involves PI3K-Akt (show AKT1 Proteins)-dependent inactivation of FOXO1a.
Sirt3 (show SIRT3 Proteins) activation is essential to improve autophagy flux by reducing the acetylation modification on FoxO1, which in turn alleviates myocardial hypertrophy.
The data reveal a novel mechanism in which the elevated miR (show MLXIP Proteins)-425 in IBD mediates pathogenic Th17 cell generation through down-regulation of Foxo1.
we found that in db/db (show LEPR Proteins) VSMC, the occupancy in promoter regions of inflammatory genes by FOXO1 was reduced.miR-135a increased the inflammatory responses of VSMC involved in complications of vascular diseases by downregulating the expression of FOXO1.
Trehalose may rescue against insulin (show INS Proteins) resistance-induced myocardial contractile defect and apoptosis, via autophagy associated with dephosphorylation of p38 MAPK (show MAPK14 Proteins) and Foxo1 without affecting phosphorylation of Akt (show AKT1 Proteins).
FoxO1 is a key mediator involved in glucose homeostasis and indicate that 1,25(OH)2D3 improves glucose metabolism and bone development
Data show that the mitochondrial enriched GCN5 (show KAT2A Proteins)-like 1 protein (GCN5L1 (show BLOC1S1 Proteins)) controls hepatic glucose production by regulating FoxO1 protein levels.
Setdb1 (show SETDB1 Proteins) regulates PTEN/AKT (show AKT1 Proteins)/FOXO1 pathway to inhibit Spermatogonial stem cells apoptosis.
These findings indicate that IGF-II reduces PGC-1alpha expression in skeletal muscle cells through a mechanism involving PI3K-Akt (show AKT1 Proteins)-FoxO1 but not p38 MAPK (show MAPK14 Proteins) or Erk1/2 MAPK (show MAPK1 Proteins) pathways.
a critical role for FOXO (show FOXO3 Proteins) transcription factors in mediating these proliferative versus apoptotic fates
L. donovani triggered AKT (show AKT1 Proteins) activation to regulate GSK-3beta/beta-catenin (show CTNNB1 Proteins)/FOXO-1 axis.
These results indicate glycine enhances muscle protein mass under an inflammatory condition. The beneficial roles of glycine on the muscle are closely associated with maintaining Akt-mTOR-FOXO1 signaling and suppressing the activation of TLR4 and/or NOD2 signaling pathways.
let-7g induces porcine granulosa cells apoptosis by inhibiting the MAP3K1 (show MAP3K1 Proteins) gene, which promotes FoxO1 expression and dephosphorylation with nuclear accumulation.
inhibition of FoxO1 expression level caused by miR (show MYLIP Proteins)-15a/b over-expression had a positive effect on adipogenesis. Thus, we conclude that miR (show MYLIP Proteins)-15a/b promote adipogenesis in porcine pre-adipocyte via repressing FoxO1
Results show that FoxO1 likely regulates MyHC I (show MYH7 Proteins) negatively and MyHC IIx and MyHC IIb (show MYH4 Proteins) positively and may play a pivotal role in the determination of muscle fiber type.
Data suggest forkhead box protein O1 (FoxO1) involvement in the regulation of TNF-related apoptosis-inducing ligand TRAIL (show TNFSF10 Proteins) and Fas ligand FasL (show FASL Proteins) expression during follicular atresia.
Data show that IL-4 (show IL4 Proteins) induces upregulation of the junction protein claudin-5 (show CLDN5 Proteins) in endothelial cells (ECs) through activation of Jak (show JAK3 Proteins)/STAT6 (show STAT6 Proteins) and phosphorylation and translocation of FoxO1 from the nucleus to the cytoplasm.
FoxO1 and C/EBPb (show CEBPB Proteins) regulate preadipocyte adipogenesis possibly through C/EBPb (show CEBPB Proteins)-> FoxO1-> C/EBPb (show CEBPB Proteins) feedback regulatory loop and FoxO1-C/EBPb (show CEBPB Proteins) protein complex.
FoxO1 delays and negatively regulates the porcine myoblast differentiation. It may also play a critical role in muscle fiber-type specification through the inhibition of myogenic regulation factors.
concluded that PI 3 (show PI3 Proteins)-kinase and Akt (show AKT1 Proteins) are activated after renal ischemia/reperfusion and that Akt (show AKT1 Proteins) phosphorylation leads to phosphorylation of FKHR and FKHRL1 (show FOXO3 Proteins), which may affect epithelial cell fate in acute renal failure.
FoxO1a can regulate p27kip nuclear localization
MicroRNA-183-96-182 cluster regulates bovine granulosa cell function by targeting FOXO1 gene.
downregulation of SIRT1 (show SIRT1 Proteins) and FoxO1 were observed in the backfat tissue of Lilu cattle with increasing age
FOXO (show FOXO3 Proteins) is a key regulator of ROS (show ROS1 Proteins)-induced apoptosis in mammalian cells.
Protein kinase A-alpha directly phosphorylates FoxO1 in vascular endothelial cells to regulate expression of vascular cellular adhesion molecule (show NCAM1 Proteins)-1 mRNA.
The results demonstrate pathways through which two different mediators, TNF-alpha (show TNF Proteins) and an advanced glycation endproduct, can induce pericyte apoptosis through activation of the transcription factor FOXO1.
FoxO1 translocation to the nucleus, and the increase in FoxO1 DNA binding activity in X. laevis liver strongly correlate with the up-regulation of manganese-dependent superoxide dismutase (show SOD1 Proteins) and catalase (show CAT Proteins) mRNA and protein levels in this organ.
This gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined\; however, it may play a role in myogenic growth and differentiation. Translocation of this gene with PAX3 has been associated with alveolar rhabdomyosarcoma.
forkhead box protein O1
, forkhead box protein O1A
, forkhead, Drosophila, homolog of, in rhabdomyosarcoma
, forkhead box O1A
, forkhead box protein O1-A
, fox family transcription factor FoxO1a.1
, foxhead box protein O1-A
, Forkhead box protein O1A
, Forkhead in rhabdomyosarcoma
, forkhead box O1A (rhabdomyosarcoma)
, forkhead box O1a
, forkhead in rhabdomyosarcoma
, forkhead protein 1
, forkhead/winged helix transcription factor FOXO1a
, forkhead box O1
, forkhead box protein O1-like