IndraLab
Statements
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"The ratio of P-Ser256 FOXO1 to total FOXO1 (a transcription factor involved in the regulation of GNG enzymes, including G6Pase and PEPCK) increased 3.0- and 3.6-fold in the 4x and 16x groups, respectively (XREF_FIG C), and analysis of total FOXO1 levels in nuclear enriched fractions detected reductions of 84 and 85%, respectively, compared with the control group (XREF_FIG C)."
reach
"It is able to induce apoptosis and inhibit proliferation in T790M positive NSCLC cell lines; upregulate the expression of forkhead box protein O1 (FoxO1); downregulate the long lncRNA colon cancer associated transcript 1 (CCAT1) levels in T790M positive NSCLC cell lines; and repress the tumor growth of T790M positive NSCLC xenografts [XREF_BIBR]."
| PMC
reach
"Carmustine but not the other two alkylating agents showed some dependency on FoxO1 in its killing RD-ES, which was consistent with the fact that cisplatin and temozolomide did not cause significant changes in the mRNA levels of FoxO1 while carmustine could significantly increase the mRNA levels of FoxO1 at 50 μM (Fig. 5g)."
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"In mice not stressed by insulin resistance, acute deletion of Foxo1 does not significantly reduce the expression of Foxo1 target genes (XREF_FIG), although chronic deletion of multiple Foxo family members including Foxo1 results in modest reduction of expression of these genes XREF_BIBR, XREF_BIBR."
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"In comparison with the model group, the levels of body mass, SOD activity, and FoxO1 and PGC-1α expression were significantly increased in the three treatment groups except SOD, expression of FoxO1 and PGC-1α in the inhibitor group ( P <0.01, P <0.05), and the contents of blood glucose, Scr, BUN, ALB, MDA and ROS were obviously decreased in the three treatment groups except ALB and ROS in the inhibitor group ( P <0.01, P <0.05)."
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"EGCG induced nuclear exclusion of FOXO1, FOXO1 binding to the hET-1 promoter, and reduction of ET-1 expression was partially inhibited by the AMPK inhibitor Compound C. Basal ET-1 protein expression was enhanced by short interfering RNA knock-down of Akt and reduced by short interfering RNA knock-down of FOXO1 or adenovirus mediated expression of dominant negative Foxo1."
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"In this study, we show that an S209A phospho-null Foxo1 exhibited Akt dependent nuclear trafficking in mouse CD8 T cells and augmented the expression of canonical Foxo1 target genes such as Il7r and Sell In contrast, an S209D phosphomimetic Foxo1 (SD-Foxo1) was largely excluded from the nucleus of CD8 T cells and failed to transactivate these genes."