Malignant tumor of colon
|
0.350 |
AlteredExpression
|
disease |
BEFREE |
We first show that the Notch-1 receptor, as well as its downstream target Hes-1, is up-regulated with colon cancer progression, similar to other genes involved in chemoresistance.
|
19147571 |
2009 |
Malignant neoplasm of lung
|
0.340 |
Biomarker
|
disease |
BEFREE |
However, Notch2-depleted tumors showed an appreciable increase in β-catenin expression, a known activator of HES1 and important lung cancer oncogene.
|
24509876 |
2015 |
Malignant neoplasm of lung
|
0.340 |
Biomarker
|
disease |
BEFREE |
Moreover, HIF1a was nearly positively correlated with HES1 in lung cancer tissues.
|
23275310 |
2013 |
Malignant neoplasm of lung
|
0.340 |
Biomarker
|
disease |
CTD_human |
In this study, we showed that a high percentage of lung cancer lines expressed Jagged1, Notch receptors, and their transcriptional target genes (HES1, Hey1), suggesting that the Notch pathway plays an important role in lung cancer biology.
|
17804716 |
2007 |
Malignant neoplasm of lung
|
0.340 |
Biomarker
|
disease |
BEFREE |
In this study, we showed that a high percentage of lung cancer lines expressed Jagged1, Notch receptors, and their transcriptional target genes (HES1, Hey1), suggesting that the Notch pathway plays an important role in lung cancer biology.
|
17804716 |
2007 |
Malignant neoplasm of lung
|
0.340 |
AlteredExpression
|
disease |
BEFREE |
HES-1 protein is detected at abundant levels in most non-NE human lung cancer cell lines which lack hASH1 but is virtually absent in hASH1-expressing lung cancer cells.
|
9144241 |
1997 |
Glioblastoma Multiforme
|
0.330 |
AlteredExpression
|
disease |
BEFREE |
Bioinformatic analysis and immunohistochemistry (IHC) were performed to evaluate the expression of Notch1 and Hes1 in GBM samples.
|
31382985 |
2019 |
Glioblastoma Multiforme
|
0.330 |
Biomarker
|
disease |
BEFREE |
Taken together, Hes1 seems to be a favorable target but not sufficient itself to target GBM efficaciously, therefore a possible pharmacological intervention should provide for the use of anti-Stat3/5 drugs either alone or in combination regimen.
|
28157712 |
2017 |
Glioblastoma Multiforme
|
0.330 |
Biomarker
|
disease |
BEFREE |
Our follow up experiment indicated that (i) an overexpression of RAMP2-AS1 reduced glioblastoma cell proliferation in vitro and also reduced glioblastoma xenograft tumors in vivo; (ii) NOTCH3 and RAMP2-AS1 coexpression rescued the inhibitory action of RAMP2-AS1 in glioblastoma cells; and (iii) RNA pull-down assay revealed a direct interaction of RAMP2-AS1 with DHC10, which may consequently inhibit, as we hypothesize, the expression of NOTCH3 and its downstream signaling molecule HES1 in glioblastoma.
|
27784795 |
2016 |
Glioblastoma Multiforme
|
0.330 |
Biomarker
|
disease |
CTD_human |
Inhibition of notch signaling blocks growth of glioblastoma cell lines and tumor neurospheres.
|
21127729 |
2010 |
Meningioma
|
0.320 |
Biomarker
|
disease |
CTD_human |
Inhibition of notch signaling blocks growth of glioblastoma cell lines and tumor neurospheres.
|
21127729 |
2010 |
Meningioma
|
0.320 |
AlteredExpression
|
disease |
BEFREE |
Activated Notch1 and Notch2 receptors induced endogenous HES1 expression and were associated with tetraploidy in meningiomas.
|
18516297 |
2008 |
Meningioma
|
0.320 |
AlteredExpression
|
disease |
BEFREE |
We have shown that the transcript and protein levels of HES1, the Notch2 and Notch1 receptors and the Jagged1 ligand are induced in meningiomas of all grades, whereas induction of TLE2 and TLE3 occurs specifically in higher-grade meningiomas.
|
15958550 |
2005 |
Glioblastoma
|
0.310 |
Biomarker
|
disease |
BEFREE |
Our follow up experiment indicated that (i) an overexpression of RAMP2-AS1 reduced glioblastoma cell proliferation in vitro and also reduced glioblastoma xenograft tumors in vivo; (ii) NOTCH3 and RAMP2-AS1 coexpression rescued the inhibitory action of RAMP2-AS1 in glioblastoma cells; and (iii) RNA pull-down assay revealed a direct interaction of RAMP2-AS1 with DHC10, which may consequently inhibit, as we hypothesize, the expression of NOTCH3 and its downstream signaling molecule HES1 in glioblastoma.
|
27784795 |
2016 |
Glioblastoma
|
0.310 |
Biomarker
|
disease |
CTD_human |
Inhibition of notch signaling blocks growth of glioblastoma cell lines and tumor neurospheres.
|
21127729 |
2010 |
Mammary Neoplasms
|
0.310 |
Biomarker
|
group |
CTD_human |
Downregulation of Notch pathway by a gamma-secretase inhibitor attenuates AKT/mammalian target of rapamycin signaling and glucose uptake in an ERBB2 transgenic breast cancer model.
|
20197467 |
2010 |
Mammary Neoplasms
|
0.310 |
Biomarker
|
group |
CTD_human |
Inhibition of Notch signaling reduces the stem-like population of breast cancer cells and prevents mammosphere formation.
|
21036696 |
2010 |
Lung Neoplasms
|
0.310 |
Biomarker
|
group |
CTD_human |
Gamma-secretase inhibitor prevents Notch3 activation and reduces proliferation in human lung cancers.
|
17804716 |
2007 |
Lung Neoplasms
|
0.310 |
AlteredExpression
|
group |
BEFREE |
In this study, we show that NOTCH signaling, as measured by the gamma-secretase cleavage product N(IC)-1, is active in both normal human and lung tumor samples; however, downstream NOTCH readouts (i.e., HES-1 and HES-5) are elevated in lung tumors.
|
17804701 |
2007 |
Mammary Neoplasms
|
0.310 |
AlteredExpression
|
group |
LHGDN |
A study on Notch signaling in human breast cancer.
|
17822320 |
2007 |
Ureteral obstruction
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
The antihelmenthic phosphate niclosamide impedes renal fibrosis by inhibiting homeodomain-interacting protein kinase 2 expression.
|
28318631 |
2017 |
Uterine Cervical Neoplasm
|
0.300 |
Biomarker
|
disease |
CTD_human |
Biological significance and therapeutic implication of resveratrol-inhibited Wnt, Notch and STAT3 signaling in cervical cancer cells.
|
25061499 |
2014 |
cervical cancer
|
0.300 |
Biomarker
|
disease |
CTD_human |
Biological significance and therapeutic implication of resveratrol-inhibited Wnt, Notch and STAT3 signaling in cervical cancer cells.
|
25061499 |
2014 |
Non-Small Cell Lung Carcinoma
|
0.300 |
Biomarker
|
disease |
CTD_human |
Notch signaling contributes to lung cancer clonogenic capacity in vitro but may be circumvented in tumorigenesis in vivo.
|
21994468 |
2011 |
oligodendroglioma
|
0.300 |
Biomarker
|
disease |
CTD_human |
Inhibition of notch signaling blocks growth of glioblastoma cell lines and tumor neurospheres.
|
21127729 |
2010 |