Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Together, our study unravels a novel mechanism by which p53 is stabilized and activated by HAUSP-mediated interaction with Bat3 and implies that Bat3 might function as a tumor suppressor through the stabilization of p53.
|
31647545 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Numerous proteins have been identified as potential substrates and binding partners of USP7; those play crucial roles in diverse array of cellular and biological processes including tumour suppression, cell cycle, DNA repair, chromatin remodelling, and epigenetic regulation.
|
29781103 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Ubiquitin specific protease 7 (USP7), the most widely studied among the nearly 100 deubiquitinating enzymes, supports cancer by positively affecting tumor growth and negatively affecting the patient's immune response to tumors.
|
28768102 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
HAUSP is a protein of immense biological importance as it is involved in several cellular processes, including host-virus interactions, oncogenesis and tumor suppression, DNA damage and repair processes, DNA dynamics and epigenetic modulations, regulation of gene expression and protein function, spatio-temporal distribution, and immune functions.
|
29967688 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
High expression of USP7 was correlated with advanced tumor stage and poor overall survival.
|
29574466 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Given the importance of USP7 in oncogenic pathways and immune-oncology, identification of USP7 inhibitors has attracted considerable interest.
|
30344943 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
We collected 121 EOC patients and analyzed the expression levels of USP7 and MARCH7 in tumor tissues with immunohistochemical staining.
|
27302477 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The tests in vitro and vivo showed a significant delay in tumor cell growth upon knockdown of USP7.
|
27590858 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Taken together, our findings demonstrate a crucial role of HAUSP in regulating N-Myc function in vivo and suggest that HAUSP inhibition is a potential therapy for MYCN-amplified tumors.
|
27618649 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Moreover, the survival rate of patients with HAUSP-positive tumors was lower when compared to that of patients with HAUSP-negative tumors.
|
23483195 |
2013 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Here, we show that expression of ubiquitin-specific protease 7 (USP7), a deubiquitylating enzyme, is decreased in STAT3-positive tumors.
|
22750444 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our data suggest that changes in HAUSP modulate tumor growth and apoptotic sensitivity in vivo.
|
18418047 |
2008 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These findings reveal an important mechanism by which p53 can be stabilized by direct deubiquitination and also imply that HAUSP might function as a tumour suppressor in vivo through the stabilization of p53.
|
11923872 |
2002 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Overexpression of the TEF-1 delta protein by transfection was oncogenic in NIH3T3 cells as evidenced by the appearance of transformed foci exhibiting anchorage-independent growth and the potential to grow as tumors in nude mice.
|
11711542 |
2002 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Tumor cell splice variants of the transcription factor TEF-1 induced by SV40 T-antigen transformation.
|
11118619 |
2000 |