Cargando…
Hsp90 inhibition differentially destabilises MAP kinase and TGF-beta signalling components in cancer cells revealed by kinase-targeted chemoproteomics
BACKGROUND: The heat shock protein 90 (Hsp90) is required for the stability of many signalling kinases. As a target for cancer therapy it allows the simultaneous inhibition of several signalling pathways. However, its inhibition in healthy cells could also lead to severe side effects. This is the fi...
Autores principales: | Haupt, Armin, Joberty, Gerard, Bantscheff, Marcus, Fröhlich, Holger, Stehr, Henning, Schweiger, Michal R, Fischer, Axel, Kerick, Martin, Boerno, Stefan T, Dahl, Andreas, Lappe, Michael, Lehrach, Hans, Gonzalez, Cayetano, Drewes, Gerard, Lange, Bodo MH |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342885/ https://www.ncbi.nlm.nih.gov/pubmed/22277058 http://dx.doi.org/10.1186/1471-2407-12-38 |
Ejemplares similares
-
Identification of Plasmodium PI4 kinase as target of MMV390048 by chemoproteomics
por: Ghidelli-Disse, Sonja, et al.
Publicado: (2014) -
Silencing the cochaperone CDC37 destabilises kinase clients and sensitises cancer cells to HSP90 inhibitors
por: Smith, Jennifer R., et al.
Publicado: (2008) -
A chemoproteomic method for identifying cellular targets of covalent kinase inhibitors
por: Chen, Ying-Chu, et al.
Publicado: (2016) -
Chemoproteomic profiling of kinases in live cells using electrophilic sulfonyl triazole probes
por: Huang, Tao, et al.
Publicado: (2021) -
The structural impact of cancer-associated missense mutations in oncogenes and tumor suppressors
por: Stehr, Henning, et al.
Publicado: (2011)