Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Surprisingly, FOXO3a was found to be excluded from the nuclei of some tumors lacking Akt-p, suggesting an Akt-independent mechanism of regulating FOXO3a localization.
|
15084260 |
2004 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Forkhead transcription factors FOXO1 (FKHR), FOXO3a (FKHRL1), and FOXO4 (AFX) play a pivotal role in tumor suppression by inducing growth arrest and apoptosis.
|
15668399 |
2005 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
We tested the hypothesis that genistein activates expression of several aberrantly silenced tumor suppressor genes (TSGs) that have unmethylated promoters such as PTEN, CYLD, p53 and FOXO3a.
|
18431742 |
2008 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Tumor suppressor FOXO3 regulates gene expression and its translocation to the cytosol leads to the abrogation of its transcriptional function.
|
19636295 |
2009 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Here, we show that depletion of FOXO3a from cancer cells leads to decreased tumor size specifically due to attenuated invasive migration.
|
19564415 |
2009 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
These findings correlate with decreased FOXO3A DNA binding activity along with down-modulation of FOXO3A transcriptional activity with increasing tumor grade.
|
19424579 |
2009 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
SGK1-sensitive mechanisms fostering tumour growth include activation of K(+) channels and Ca(2+) channels, Na(+)/H(+) exchanger, amino acid transporters and glucose transporters, upregulation of the nuclear factor NFkappaB and beta-catenin as well as downregulation of the transcription factors Foxo3a/FKHRL1 and p53.
|
20541034 |
2010 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Epidermal growth factor (EGF)-induced proliferation of colon cancer cells plays an important role in colon cancer progression and is mediated by loss of tumor suppressor FOXO3 activity.
|
21639915 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Forkhead box O3 (FOXO3) has a wide range of functions: it promotes tumor suppression, cell cycle arrest, repair of damaged DNA, detoxification of reactive oxygen species, apoptosis and plays a pivotal role in promoting longevity.
|
21725602 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Rapamycin combined with cisplatin as its feedback Akt activation inhibitor revealed the most dramatic FOXO3a nuclear localization and reactivation with the prevention of its feedback loop and exposed significant synergistic effects of decreased cell proliferation and increased apoptosis in vitro and decreased tumor size in vivo.
|
21092744 |
2011 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, we show that FoxO3A is activated in human hypoxic tumour tissue in vivo and that FoxO3A short-hairpin RNA (shRNA)-expressing xenograft tumours are decreased in size and metabolically changed.
|
21915097 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
PRDM1 and FOXO3 are considered to play an important role in the pathogenesis of NK-cell neoplasms.
|
21690554 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Finally, resveratrol-treated mice showed significant inhibition in tumor growth which was associated with reduced phosphorylation of ERK, PI3K, AKT, FOXO1 and FOXO3a, and induction of apoptosis and FOXO target genes.
|
21980390 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Overall, these results support RNAi-mediated silencing of Foxo3 as an effective strategy to enhance the therapeutic antitumor effect of HER-2/neu DNA vaccines against p185neu-positive tumors.
|
21107437 |
2011 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
The results of this study revealed that the oncogenic effect of BRAF(V600E) is associated with the inhibition of MST1 tumor suppressor pathways, and that the activity of RASSF1A-MST1-FoxO3 pathways determines the phenotypes of BRAF(V600E) tumors.
|
21249150 |
2011 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Forkhead transcription factor FOXO3a protein activates nuclear factor κB through B-cell lymphoma/leukemia 10 (BCL10) protein and promotes tumor cell survival in serum deprivation.
|
22474286 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We recently demonstrated that p38α is required to maintain colorectal cancer (CRC) metabolism, as its inhibition leads to FoxO3A activation, autophagy, cell death, and tumor growth reduction both in vitro and in vivo.
|
22579651 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
FOXO3A has been implicated in tumor suppression and GC-induced apoptosis, suggesting that FOXO3A has potential as a therapeutic target.
|
22582938 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Importantly, Ad-FKHRL1/TM treatment of subcutaneous melanoma xenografts in mice resulted in approximately 70% decrease in tumor size compared with controls.
|
22892845 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These combined data suggest an entirely novel function for FoxO3a in ATC promotion by enhancing cell cycle progression and tumor growth through transcriptional upregulation of cyclin A1.
|
22718346 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Despite the central role of FOXO3 as a tumour suppressor and phosphatidylinositol 3-kinase (PI3K)/AKT effector, little is known about its involvement in mantle cell lymphoma (MCL) biology.
|
22107151 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Injection of Ad-FOXO3a-TM suppressed the growth of xenograft tumors in athymic mice.
|
21974806 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In summary, our results show that selenite could induce ROS-dependent FoxO3a-mediated apoptosis in CRC cells and xenograft tumors through PTEN-mediated inhibition of the PI3K/AKT survival axis.
|
23392169 |
2013 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In this study, we report upregulation of the oncomir microRNA (miR)-205 in multiple subtypes of NSCLC, which directly represses PTEN and PHLPP2 expression and activates both the AKT/FOXO3a and AKT/mTOR signaling pathways. miR-205 overexpression in NSCLC cells accelerated tumor cell proliferation and promoted blood vessel formation in vitro and in vivo.
|
23856247 |
2013 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The tumour suppressor FOXO3a increases its levels of acetylation in MEFs depleted of SIRT6, whereas its induction by epirubicin is attenuated in breast cancer cells overexpressing SIRT6.
|
23514751 |
2013 |