CTSB, cathepsin B, 1508

N. diseases: 304; N. variants: 17
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0376358
Disease: Malignant neoplasm of prostate
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
CUI: C0376358
Disease: Malignant neoplasm of prostate
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
CUI: C0376358
Disease: Malignant neoplasm of prostate
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
CUI: C0376358
Disease: Malignant neoplasm of prostate
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
CUI: C0376358
Disease: Malignant neoplasm of prostate
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
CUI: C0376358
Disease: Malignant neoplasm of prostate
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
CUI: C0376358
Disease: Malignant neoplasm of prostate
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
CUI: C0017638
Disease: Glioma
Glioma
0.300 Biomarker disease BEFREE In contrast, immunostaining of glioma tissue for CD68 and for cathepsin B may be used for prognosis of survival in these patients. 19661345 2009
CUI: C0017638
Disease: Glioma
Glioma
0.300 AlteredExpression disease BEFREE Mechanism of p27 upregulation induced by downregulation of cathepsin B and uPAR in glioma. 21840777 2011
CUI: C0017638
Disease: Glioma
Glioma
0.300 Biomarker disease BEFREE uPAR and cathepsin B-mediated compartmentalization of JNK regulates the migration of glioma-initiating cells. 24699410 2014
CUI: C0017638
Disease: Glioma
Glioma
0.300 AlteredExpression disease BEFREE In conclusion, our results show that downregulation of cathepsin B and uPAR alone and in combination inhibit glioma cell adhesion by downregulating CD151 and its associated signaling molecules in vitro and in vivo. 22495828 2013
CUI: C0017638
Disease: Glioma
Glioma
0.300 AlteredExpression disease BEFREE Glioma is the most commonly diagnosed primary brain tumor and is characterized by invasive and infiltrative behavior. uPAR and cathepsin B are known to be overexpressed in high-grade gliomas and are strongly correlated with invasive cancer phenotypes. 21060833 2010
CUI: C0017638
Disease: Glioma
Glioma
0.300 AlteredExpression disease BEFREE Radiation treatment significantly enhanced uPAR and cathepsin B levels in glioma-initiating cells. 22573309 2012
CUI: C0017638
Disease: Glioma
Glioma
0.300 Biomarker disease BEFREE We observed progressive reductions in levels of the protease inhibitor cystatin C, an inhibitor of cathepsin B with corresponding increases in the malignancy of glioma cell lines, implying an inverse correlation between cystatin C and tumor grade. 12483523 2002
CUI: C0017638
Disease: Glioma
Glioma
0.300 Biomarker disease BEFREE These results demonstrate the potential of pMU and pMC as therapeutic candidates for the treatment of glioma. 22076676 2012
CUI: C0017638
Disease: Glioma
Glioma
0.300 Biomarker disease BEFREE Considering the existence of integrin inhibitor-resistant cancer cells, our study provides a novel and effective approach to inhibiting integrins by downregulating MMP-9, uPAR and cathepsin B in the treatment of glioma. 20657647 2010
CUI: C0017638
Disease: Glioma
Glioma
0.300 AlteredExpression disease BEFREE Our previous work and that of others strongly suggest a relationship between the infiltrative phenotype of glioma and the expression of cathepsin B and uPAR. 20661471 2010
CUI: C0017638
Disease: Glioma
Glioma
0.300 AlteredExpression disease BEFREE Cystatin E/M is a potent inhibitor of cathepsin B, which is frequently overexpressed in glioma. 18607344 2008
CUI: C0017638
Disease: Glioma
Glioma
0.300 Biomarker disease BEFREE Given that sustained ATP release from glia upon injury greatly contributes to secondary brain damage and cathepsin B plays a critical role in glioma dissemination, TI-VAMP silencing can represent a novel strategy to control lysosome fusion in pathological conditions. 22188132 2012
CUI: C0017638
Disease: Glioma
Glioma
0.300 AlteredExpression disease BEFREE Glioma spheroids expressed higher levels of cathepsin B than did monolayers and the ability of subclones differing in cathepsin B activity to infiltrate normal brain aggregates paralleled their cathepsin B activity. 10571410 1999
CUI: C0017638
Disease: Glioma
Glioma
0.300 AlteredExpression disease BEFREE We have shown previously that urokinase plasminogen activator receptor (uPAR) and cathepsin B are overexpressed during glioma progression, particularly at the leading edge of the tumor. 15205313 2004
CUI: C0017638
Disease: Glioma
Glioma
0.300 AlteredExpression disease BEFREE Cathepsin B expression and localization in glioma progression and invasion. 7954439 1994
CUI: C0017638
Disease: Glioma
Glioma
0.300 Biomarker disease BEFREE Furthermore, IL-1β, phosphorylated Akt, and cathepsin B proteins were also reduced in MSC/glioma. 23034897 2013
CUI: C0017638
Disease: Glioma
Glioma
0.300 AlteredExpression disease BEFREE Cathepsin B and uPAR knockdown inhibits tumor-induced angiogenesis by modulating VEGF expression in glioma. 21394106 2011
CUI: C0017638
Disease: Glioma
Glioma
0.300 Biomarker disease BEFREE Transcription of human cathepsin B is mediated by Sp1 and Ets family factors in glioma. 10701774 2000