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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Aug 2016.

FBP folate binding protein

fbp1
Top mentioned proteins: ACID, CAN, HAD, phosphoenolpyruvate carboxykinase, V1a
Papers on fbp1
Alternate metabolic programs define regional variation of relevant biological features in renal cell carcinoma progression.
New
Rathmell et al., Chapel Hill, United States. In Clin Cancer Res, Feb 2016
RESULTS: Tumor subsamples displayed a range of heterogeneity for common features of HIF expression and microvessel density, as well as for features closely linked to metabolic processes, such as GLUT1 and FBP1.
Prognostic Impact of Novel Molecular Subtypes of Small Intestinal Neuroendocrine Tumor.
New
Thirlwell et al., London, United Kingdom. In Clin Cancer Res, Feb 2016
Epimutations were found at a recurrence rate of up to 85%, and 21 epigenetically dysregulated genes were identified, including CDX1 (86%), CELSR3 (84%), FBP1 (84%), and GIPR (74%).
The effect of insulin on plasma glucose concentrations, expression of hepatic glucose transporters and key gluconeogenic enzymes during the perinatal period in broiler chickens.
New
Everaert et al., Leuven, Belgium. In Gen Comp Endocrinol, Jan 2016
However, little is known about the response of insulin on plasma glucose concentrations and mRNA abundance of hepatic glucose transporters 1, 2, 3, 8, 9 and 12 (GLUT 1, 2, 3, 8, 9 and 12) and three regulatory enzymes of the gluconeogenesis, phosphoenolpyruvate carboxykinase 1 and 2 (PCK 1 and 2) or fructose-1,6-biphosphatase 1 (FBP1) in chicks during the perinatal period.
An RNA interference screen identifies new avenues for nephroprotection.
New
Kandel et al., Buffalo, United States. In Cell Death Differ, Dec 2015
We used an RNA interference screen to identify genes (BCL2L14, BLOC1S2, C2ORF42, CPT1A, FBP1, GCNT3, RHOB, SCIN, TACR1, and TNFAIP6) whose suppression improves survival of kidney epithelial cells in in vitro models of oxygen and glucose deprivation.
Down-regulation of FBP1 by ZEB1-mediated repression confers to growth and invasion in lung cancer cells.
New
Li et al., China. In Mol Cell Biochem, Dec 2015
Here, we demonstrated that FBP1 (Fructose-1, 6-bisphosphatase) was frequently down-regulated in lung cancer tissues and cells, and FBP1 down-regulation was associated with poor prognosis in lung cancer patients.
NPM1 activates metabolic changes by inhibiting FBP1 while promoting the tumorigenicity of pancreatic cancer cells.
New
Peng et al., Shanghai, China. In Oncotarget, Sep 2015
We also identified NPM1 could stimulate aerobic glycolysis and repress fructose-1, 6-bisphosphatase 1 (FBP1) in pancreatic cancer cells.
FUSE Binding Protein 1 Facilitates Persistent Hepatitis C Virus Replication in Hepatoma Cells by Regulating Tumor Suppressor p53.
New
Pandey et al., Newark, United States. In J Virol, Aug 2015
Immunohistochemistry of archived HCC tumors showed abundant FBP1 expression in HCC tumors with the CHC background.
Alteration of factors associated with hepatic gluconeogenesis in response to acute lipopolysaccharide in dairy goat.
New
Song et al., In J Anim Sci, Jun 2015
In liver tissue, the mRNA of key gluconeogenic enzymes, phosphoenolpyruvate carboxykinase 1 (PEPCK1;P < 0.05), fructose-1,6-bisphosphatase 1 (FBP1;P < 0.01), pyruvate carboxylase (PCB;P < 0.05), and acyl-CoA synthetase short-chain family member 3 (ACSS3; < 0.01), in the related pathways and PPAR-γ coactivator 1α (PGC-1α;P < 0.05) were decreased in the LPS group compared with those in the control group, whereas glucose-6-phosphatase (G6Pase-α) was not different (P > 0.05).
Far upstream element-binding protein 1 is a prognostic biomarker and promotes nasopharyngeal carcinoma progression.
Zeng et al., Guangzhou, China. In Cell Death Dis, 2014
Previous studies identified that far upstream element-binding protein 1 (FBP1), a transcriptional regulator of c-Myc that is one of the most frequently aberrantly expressed oncogenes in various human cancers, including NPC, is an important biomarker for many cancers.
Fructose-1,6-bisphosphatase opposes renal carcinoma progression.
Impact
Simon et al., Philadelphia, United States. In Nature, 2014
Here we used an integrative approach comprising pan-metabolomic profiling and metabolic gene set analysis and determined that the gluconeogenic enzyme fructose-1,6-bisphosphatase 1 (FBP1) is uniformly depleted in over six hundred ccRCC tumours examined.
Far upstream element binding protein 1: a commander of transcription, translation and beyond.
Review
Chen et al., Tucson, United States. In Oncogene, 2013
This review summarizes biochemical features of FBP1, its mechanism of action, FBP family members and the involvement of FBP1 in carcinogenesis.
Loss of FBP1 by Snail-mediated repression provides metabolic advantages in basal-like breast cancer.
Impact
Zhou et al., Lexington, United States. In Cancer Cell, 2013
We show that the Snail-G9a-Dnmt1 complex, which is critical for E-cadherin promoter silencing, is also required for the promoter methylation of fructose-1,6-biphosphatase (FBP1) in basal-like breast cancer (BLBC).
Host factors in enterovirus 71 replication.
Review
Li et al., Taiwan. In J Virol, 2011
Three of these proteins, heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1), far-upstream element-binding protein 2 (FBP2), and FBP1 are nuclear proteins which in EV71-infected cells are relocalized to the cytoplasm, and they influence EV71 internal ribosome entry site (IRES) activity.
Stepwise chromatin remodelling by a cascade of transcription initiation of non-coding RNAs.
Impact
Ohta et al., Wako, Japan. In Nature, 2008
Here we show that RNA polymerase II (RNAPII) transcription of ncRNAs is required for chromatin remodelling at the fission yeast Schizosaccharomyces pombe fbp1(+) locus during transcriptional activation.
The involvement of AU-rich element-binding proteins in p38 mitogen-activated protein kinase pathway-mediated mRNA stabilisation.
Review
Saklatvala et al., London, United Kingdom. In Cell Signal, 2004
In recent years, AREs have shown to be binding sites for numerous proteins including HuR, TTP, AUF1, AUF2, FBP1, FBP2 (KSRP), TIA-1, and TIAR.
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