Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Neither baseline tumor expression of AURKA (ROC = 0.57, P = 0.46) nor AURKB (ROC = 0.56, P = 0.87) predicted for ypT2-4 status.
|
31597600 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We did a CRISPR/Cas9-based screen that showed that <i>RB1</i><sup>-/-</sup> SCLC are hyperdependent on <i>AURKB</i>, likely because both genes control mitotic fidelity, and confirmed that Aurora B kinase inhibitors are efficacious against <i>RB1</i><sup>-/-</sup> SCLC tumors in mice at nontoxic doses.<i>See related commentary by Dick and Li, p. 169</i>.<i>This article is highlighted in the In This Issue feature, p. 151</i>.
|
30373918 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, aurora B was positively related to grading and tumor size and negatively to differentiation and functionality.
|
29970506 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Knocking down of Aurora B with shRNA substantially inhibited HCC cell proliferation, colony formation and delayed tumor growth in nude mice.
|
30263005 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Chromosome instability in tumor cells due to defects in Aurora B mediated error correction at kinetochores.
|
30513041 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Tumor growth was significantly lower in AKB-LfNPs alone and in combination with TMZ treated mice and increased the survival by 2.5-times.
|
30334671 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In comparative <i>in vivo</i> experiments, GS-5829 and/or GS-626510 were found more effective than JQ1 at the concentrations/doses used in decreasing tumor growth in both USC-ARK1 and USC-ARK2 mouse xenograft models.<b>Conclusions:</b> GS-5829 and GS-626510 may represent novel, highly effective therapeutics agents against recurrent/chemotherapy-resistant USC-overexpressing c-Myc.
|
29941483 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
SIX3 is a novel negative transcriptional regulator and acts as a tumor suppressor that directly represses the transcription of AURKA and AURKB in astrocytoma.
|
28595628 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The results of experiment indicated that specific knockdown of Aurora kinase B led to prostate carcinoma cells apoptosis and inhibited tumor growth.
|
28100163 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
aurora B kinase is highly expressed in several cancer cells and promotes tumorigenesis and progression, and therefore, it is an important target for drug to treat tumors.
|
27704720 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, we found that the tumor suppressive effect of Aurora-B and HDAC inhibition is due to the induction of cell cycle arrest and/or apoptosis.
|
26638998 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Univariate, multivariate and Kaplan-Mayer analyses documented the lack of association between Aurora-A or Aurora-B expression and clinicopathological parameters such as gender, age, tumor size, histology, TNM stage, lymph node metastasis and BRAF status as well as disease recurrences or disease-free interval.
|
25807528 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Informative TMA results were obtained in 91 tumor cases for Aurora-B and 93 tumor cases for FOXM1.
|
25986250 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Histone H3 phosphorylation precedes the induction of apoptosis in p53-/- tumour cell lines but does not appear to be required for this fate as an Aurora kinase inhibitor suppresses phosphorylation of both Aurora B and histone H3 but has little effect on cell death.
|
24853431 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In addition, dual therapy with trastuzumab and lapatinib resulted in significant antitumor activity only in ARK2 and EnCa1 tumors.
|
25294905 |
2014 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Aurora B expression in tumor and non-tumor tissue was examined by use of quantitative reverse transcription-polymerase chain reaction.
|
23893130 |
2014 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In vivo xenograft studies indicated decreased tumor growth and decreased aurora B kinase activity in mice treated with low-dose AMG 900 and vorinostat compared to either agent alone.
|
24989836 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Intravenous VVNIS-C was more effective at controlling AN3 CA xenograft growth than VVNIS-W, while both VVNIS-C and VVNIS-W ceased tumor growth and induced tumor regression in 100% of mice bearing ARK-2 xenografts.
|
24434058 |
2014 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Our results suggest that AURKA and AURKB overexpression in pediatric ACT may be related to more aggressive disease and the inhibition of these proteins could be an interesting approach for the treatment of these tumors.
|
23788275 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The cytosolic staining intensity of the ARK2 protein was associated with tumor stage (p = 0.006) and tumor size (T) of TNM staging system (p = 0.026).
|
23504335 |
2013 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Involvement of aurora kinase B (AURKB) and Wee1-like protein kinase (WEE1) as downstream proteins in the (V600E)B-RAF pathway was validated in xenografted tumors, and mechanisms of action were characterized in size- and time-matched tumors.
|
23416158 |
2013 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Aurora-B overexpression was found in 83 cases (53%) of NSCLC, and was significantly correlated with vascular invasion (p=0.012), poor differentiation (p<0.001), larger tumor size (p=0.010) and lymph node metastasis (p=0.05) and poor prognosis (p=0.011).
|
23313006 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Aurora B kinase and survivin, major components of the CPC, were particularly upregulated in high-grade carcinomas and may therefore comprise therapeutic targets for these tumors.
|
23929435 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Compared with peripheral T-cell lymphoma, not otherwise specified and normal γδ T cells, HSTL overexpressed genes encoding NK-cell-associated molecules, oncogenes (FOS and VAV3), the sphingosine-1-phosphatase receptor 5 involved in cell trafficking, and the tyrosine kinase SYK, whereas the tumor-suppressor gene AIM1 (absent in melanoma 1) was among the most down-expressed.
|
22510872 |
2012 |
Neoplasms
|
0.100 |
PosttranslationalModification
|
group |
BEFREE |
LINE-1 hypomethylation and AIM1 hypermethylation have prognostic utility in both melanoma patients' tumors and serum.
|
22402438 |
2012 |