Polycystic Ovary Syndrome
|
0.320 |
Biomarker
|
disease |
MGD |
Young PKBβ knockout mice were used to model PCOS by treatment with LH and exhibited a cyst area that was threefold greater than in controls, but without hyperinsulinemia.
|
22275470 |
2012 |
Hyperinsulinism
|
0.040 |
Biomarker
|
disease |
BEFREE |
Young PKBβ knockout mice were used to model PCOS by treatment with LH and exhibited a cyst area that was threefold greater than in controls, but without hyperinsulinemia.
|
22275470 |
2012 |
Polycystic Ovary Syndrome
|
0.320 |
Biomarker
|
disease |
BEFREE |
Young PKBβ knockout mice were used to model PCOS by treatment with LH and exhibited a cyst area that was threefold greater than in controls, but without hyperinsulinemia.
|
22275470 |
2012 |
Secondary malignant neoplasm of liver
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Xenografts established by injecting AKT2 silenced human neuroblastoma cells into murine spleen expressed decreased levels of AKT2 and resulted in fewer liver metastases compared to controls in vivo.
|
23468863 |
2013 |
Neuroblastoma
|
0.040 |
Biomarker
|
disease |
BEFREE |
Xenografts established by injecting AKT2 silenced human neuroblastoma cells into murine spleen expressed decreased levels of AKT2 and resulted in fewer liver metastases compared to controls in vivo.
|
23468863 |
2013 |
Central neuroblastoma
|
0.040 |
Biomarker
|
disease |
BEFREE |
Xenografts established by injecting AKT2 silenced human neuroblastoma cells into murine spleen expressed decreased levels of AKT2 and resulted in fewer liver metastases compared to controls in vivo.
|
23468863 |
2013 |
Childhood Neuroblastoma
|
0.040 |
Biomarker
|
disease |
BEFREE |
Xenografts established by injecting AKT2 silenced human neuroblastoma cells into murine spleen expressed decreased levels of AKT2 and resulted in fewer liver metastases compared to controls in vivo.
|
23468863 |
2013 |
Metabolic Diseases
|
0.020 |
Biomarker
|
group |
BEFREE |
While the roles of Akt1 and Akt2 in metabolism are well established, it is not yet known whether Akt3 plays a role in metabolic diseases.
|
29202451 |
2017 |
Hepatocarcinogenesis
|
0.020 |
Biomarker
|
disease |
BEFREE |
While AKT2 is the major isoform downstream of activated phosphoinositide 3-kinase and loss of phosphatase and tensin homolog-induced HCC, the precise function of AKT1 in hepatocarcinogenesis is largely unknown.
|
31062368 |
2019 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
While AKT2 is the major isoform downstream of activated phosphoinositide 3-kinase and loss of phosphatase and tensin homolog-induced HCC, the precise function of AKT1 in hepatocarcinogenesis is largely unknown.
|
31062368 |
2019 |
Liver carcinoma
|
0.300 |
Biomarker
|
disease |
BEFREE |
Whereas combined Akt1 and Akt2 rapidly induced mortality, hepatic Akt inhibition induced liver injury that promotes hepatocellular carcinoma.
|
28557977 |
2017 |
Glioblastoma Multiforme
|
0.090 |
AlteredExpression
|
disease |
BEFREE |
When combined with AEG-1 silencing, conditional expression of Akt2-PH markedly increased survival in an orthotopic mouse model of human GBM.
|
25304263 |
2014 |
Malignant neoplasm of pancreas
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
We suggest that AKT2 inhibition abrogates gemcitabine-induced activation of AKT2 and NF-κB, and promotes gemcitabine-induced PUMA upregulation, resulting in chemosensitization of pancreatic tumors to gemcitabine, which is probably an important strategy for the treatment of pancreatic cancer.
|
22312312 |
2012 |
Pancreatic carcinoma
|
0.360 |
AlteredExpression
|
disease |
BEFREE |
We suggest that AKT2 inhibition abrogates gemcitabine-induced activation of AKT2 and NF-κB, and promotes gemcitabine-induced PUMA upregulation, resulting in chemosensitization of pancreatic tumors to gemcitabine, which is probably an important strategy for the treatment of pancreatic cancer.
|
22312312 |
2012 |
Pancreatic Neoplasm
|
0.320 |
AlteredExpression
|
disease |
BEFREE |
We suggest that AKT2 inhibition abrogates gemcitabine-induced activation of AKT2 and NF-κB, and promotes gemcitabine-induced PUMA upregulation, resulting in chemosensitization of pancreatic tumors to gemcitabine, which is probably an important strategy for the treatment of pancreatic cancer.
|
22312312 |
2012 |
Adenocarcinoma of lung (disorder)
|
0.040 |
GeneticVariation
|
disease |
BEFREE |
We simultaneously analyzed somatic mutations in EGFR, ERBB2, K-RAS, PIK3CA and BRAF genes in the 3 samples with the AKT2 mutations, and found a lung adenocarcinoma with the AKT2 missense mutation harbored an EGFR mutation.
|
17047397 |
2006 |
Squamous cell carcinoma of esophagus
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
We selected five potentially functional SNPs in AKT1 (rs2494750, rs2494752 and rs10138277) and AKT2 (rs7254617 and rs2304186) genes and investigated their associations with ESCC risk in 1117 ESCC cases and 1096 controls in an Eastern Chinese population.
|
26828791 |
2016 |
Pulmonary Fibrosis
|
0.010 |
Biomarker
|
disease |
BEFREE |
We report that AKT2 deficiency (<i>Akt2</i><sup>-/-</sup>) protected against bleomycin-induced pulmonary fibrosis and inflammation.
|
28455433 |
2017 |
Photoreceptor degeneration
|
0.010 |
Biomarker
|
disease |
BEFREE |
We previously reported that Akt2 knockout mice were susceptible to light stress-induced photoreceptor degeneration, whereas Akt1 deletion had no effect on the retina.
|
29721991 |
2018 |
Insulin-resistant diabetes mellitus
|
0.110 |
GeneticVariation
|
disease |
BEFREE |
We previously reported a family in which a heterozygous missense mutation in Akt2 led to a dominantly inherited syndrome of insulin-resistant diabetes and partial lipodystrophy.
|
17327441 |
2007 |
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
|
0.010 |
Biomarker
|
disease |
BEFREE |
We previously demonstrated that the tumorigenicity and invasiveness of pancreatic ductal adenocarcinoma (PDAC) cell lines with amplified AKT2 could be markedly reduced by transfection with antisense AKT2 constructs.
|
9496907 |
1998 |
Carcinogenesis
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
We previously demonstrated that AKT2 plays critical roles in the regulation of neuroblastoma tumorigenesis.
|
31608140 |
2019 |
Non-Small Cell Lung Carcinoma
|
0.460 |
Biomarker
|
disease |
BEFREE |
We present the first evidence that miR-608 behaves as a tumour suppressor in A549 and SK-LU-1 cells through the regulation of AKT2, suggesting that selective targeting of AKT2 via miR-608 may be developed as a potential therapeutic strategy for miRNA-based non-small cell lung cancer (NSCLC) therapy.
|
29075783 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We present the first evidence that miR-608 behaves as a tumour suppressor in A549 and SK-LU-1 cells through the regulation of AKT2, suggesting that selective targeting of AKT2 via miR-608 may be developed as a potential therapeutic strategy for miRNA-based non-small cell lung cancer (NSCLC) therapy.
|
29075783 |
2017 |
Stage IV Ovarian Carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We obtained primary ovarian carcinoma samples as well as ascitic fluid and distantly metastatic ovarian carcinoma to examine the expression of Akt2.
|
25894377 |
2015 |