Co-depletion of cathepsin B and uPAR induces G0/G1 arrest in glioma via FOXO3a mediated p27 upregulation.
<h4>Background</h4>Cathepsin B and urokinase plasminogen activator receptor (uPAR) are both known to be overexpressed in gliomas. 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....
Guardado en:
Autores principales: | Sreelatha Gopinath, Rama Rao Malla, Christopher S Gondi, Kiranmai Alapati, Daniel Fassett, Jeffrey D Klopfenstein, Dzung H Dinh, Meena Gujrati, Jasti S Rao |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2010
|
Materias: | |
Acceso en línea: | https://doaj.org/article/b2fcc1f333f74a17998223b24a0a18cf |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Downregulation of uPAR and cathepsin B induces apoptosis via regulation of Bcl-2 and Bax and inhibition of the PI3K/Akt pathway in gliomas.
por: Ramarao Malla, et al.
Publicado: (2010) -
MMP-9, uPAR and cathepsin B silencing downregulate integrins in human glioma xenograft cells in vitro and in vivo in nude mice.
por: Krishna Kumar Veeravalli, et al.
Publicado: (2010) -
Upregulation of PTEN in glioma cells by cord blood mesenchymal stem cells inhibits migration via downregulation of the PI3K/Akt pathway.
por: Venkata Ramesh Dasari, et al.
Publicado: (2010) -
SPARC overexpression inhibits cell proliferation in neuroblastoma and is partly mediated by tumor suppressor protein PTEN and AKT.
por: Praveen Bhoopathi, et al.
Publicado: (2012) -
MMP-2 siRNA inhibits radiation-enhanced invasiveness in glioma cells.
por: Aruna Venkata Badiga, et al.
Publicado: (2011)