Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Continuative analyses revealed the molecular and immunological correlates of RIG-I expression in the tumor microenvironment, including interferon production and a distinct immune-regulatory signature involving checkpoint molecules (PD-L1/PD-1), the RNA-editing enzyme ADAR1, and the regulatory T cell-specific transcription factor FoxP3.
|
31800094 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
A protein hub that involves the double-stranded RNA (dsRNA) editing enzyme adenosine deaminase RNA specific (ADAR), the RNase DICER1, and the dsRNA-activated kinase protein activator of PKR (PACT) mediates many of these tumor-intrinsic responses, with in vitro ADAR dependency varying by tumor type (range 11-80%).
|
31174840 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Immunohistochemistry analysis of ADAR1 showed different expressions between normal mucosa and tumor tissue.
|
30489667 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
For in vivo experiments, a xenograft model where OSCC cells stably expressing ADAR1 were implanted was used to investigate the effect of ADAR1 on tumor growth and progression, and the expression of ADAR1, PCNA, SOX2 and POU5F1 was further detected by immunohistochemistry.
|
31315644 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Previously we have reported that metastatic melanoma cell lines and tumor specimens have reduced expression of ADAR1 and consequently are impaired in their ability to perform A-to-I microRNA (miRNA) editing.
|
29386624 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Immunohistochemical analyses of tumor and paired normal samples from 16 gastric cancer patients showed that ADAR1 expression was higher in tumors than in normal tissues and inversely correlated with PHACTR4 staining.
|
29691780 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Among patients with lymph node metastasis, those with high tumour-infiltrating lymphocyte levels and low ADAR1 expression demonstrated the best disease-free survival.
|
29022489 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
One-factor analysis revealed that ADAR1 was significantly correlated with tumor diameter, horizontal diffusion diameter, vascular invasion, parametrial invasion, vaginal involvement, and pathologically diagnostic criteria for perineural invasion (PNI).
|
28109322 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Herein we show that the adenosine-to-inosine editing enzyme ADAR1 undergoes gene amplification in non-small cancer cell lines and primary tumors in association with higher levels of the corresponding mRNA and protein.
|
26640150 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Here we investigate the role of ADAR1 in melanoma immune resistance.Importantly, knockdown of ADAR1 in human melanoma cells induces resistance to tumor infiltrating lymphocytes in a cell contact-dependent mechanism.
|
26338962 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In vitro and in vivo functional assays prove that ADAR1 functions as an oncogene while ADAR2 has tumour suppressive ability in HCC.
|
23766440 |
2014 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Among the three ADAR enzymes expressed in human cells, only ADAR1 was overexpressed in primary ESCC tumors.
|
24302582 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MicroRNA-mediated loss of ADAR1 in metastatic melanoma promotes tumor growth.
|
23728176 |
2013 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
A→I editing of AZIN1 transcripts, specifically regulated by ADAR1 (encoding adenosine deaminase acting on RNA-1), results in a serine-to-glycine substitution at residue 367 of AZIN1, located in β-strand 15 (β15) and predicted to cause a conformational change, induced a cytoplasmic-to-nuclear translocation and conferred gain-of-function phenotypes that were manifested by augmented tumor-initiating potential and more aggressive behavior.
|
23291631 |
2013 |