Malignant neoplasm of prostate
|
0.390 |
Biomarker
|
disease |
BEFREE |
RD-N, an aminomethylated derivative of riccardin D, is a lysosomotropic agent that can trigger lysosomal membrane permeabilization followed by cathepsin B (CTSB)-dependent apoptosis in prostate cancer (PCa) cells, but the underlying mechanisms remain unknown.
|
30565390 |
2019 |
Malignant neoplasm of prostate
|
0.390 |
Biomarker
|
disease |
BEFREE |
Together, these results demonstrate the critical role of MTA1 as an upstream regulator of CTSB-mediated events associated with cell invasiveness and raise the possibility that targeting MTA1/CTSB signaling in the tumor may prevent the development of bone metastasis in prostate cancer.
|
30027683 |
2018 |
Malignant neoplasm of prostate
|
0.390 |
Biomarker
|
disease |
BEFREE |
We demonstrated the importance of cathepsin B degradable linker from the context of drug content and different prostate cancer cell lines.
|
28913790 |
2017 |
Malignant neoplasm of prostate
|
0.390 |
AlteredExpression
|
disease |
BEFREE |
These results demonstrate a novel pathway by which AC, through S1P, promotes an invasive phenotype in prostate cancer by causing overexpression and secretion of cathepsin B through activation and nuclear expression of Ets1.
|
22322590 |
2012 |
Malignant neoplasm of prostate
|
0.390 |
AlteredExpression
|
disease |
BEFREE |
Here we show that androgen deprivation therapy (ADT), a widely used treatment for advanced prostate cancer, induces a senescence-associated secretory phenotype in prostate cancer epithelial cells, indicated by increases in senescence-associated β-galactosidase activity, heterochromatin protein 1β foci, and expression of cathepsin B and insulin-like growth factor binding protein 3.
|
21677876 |
2011 |
Malignant neoplasm of prostate
|
0.390 |
GeneticVariation
|
disease |
BEFREE |
Polymorphism L26V in the cathepsin B gene may be associated with a risk of prostate cancer and differentiation.
|
19930869 |
2010 |
Malignant neoplasm of prostate
|
0.390 |
Biomarker
|
disease |
BEFREE |
In this study, the therapeutic potential of siRNA-mediated targeting of matrix metalloproteinase-9 (MMP-9), urokinase plasminogen activator receptor (uPAR), and cathepsin B (CB) in prostate cancer was carried out using single and bi-cistronic siRNA-expressing constructs.
|
20448670 |
2010 |
Malignant neoplasm of prostate
|
0.390 |
Biomarker
|
disease |
CTD_human |
Frequent loss of cystatin E/M expression implicated in the progression of prostate cancer.
|
19503093 |
2009 |
Malignant neoplasm of prostate
|
0.390 |
AlteredExpression
|
disease |
BEFREE |
This paper is a review of studies using these novel markers in order to determine whether prostate cancer patients with the following characteristics have more aggressive cancer than those without: a) high serum levels of cathepsin B, survivin, Her - 2 / neu, IGFBP-2; b) low serum stefin A, IGFBP-3, c) positive immuno-staining of primary tumors for Her-2/neu, survivin and cathepsin B / stefin A ratio > 1 and d) gene expression of AMACR, HER-2/neu, high Bcl-2: Bax ratio and EZH2 in cancer cells.
|
18405443 |
2008 |
Malignant neoplasm of prostate
|
0.390 |
GeneticVariation
|
disease |
BEFREE |
Our objective was to determine the relationship of CB and stefin A (cystatin A) mRNA localization to the Gleason grading system for histologic scores in the hope of distinguishing aggressive and less aggressive variants of prostate cancer.
|
10652560 |
2000 |