Cargando…
Inhibition of PLK1 Destabilizes EGFR and Sensitizes EGFR-Mutated Lung Cancer Cells to Small Molecule Inhibitor Osimertinib
SIMPLE SUMMARY: Despite the clinical use of epidermal growth factor receptor (EGFR) inhibitors for non-small cell lung cancer (NSCLC) patients, this disease remains incurable due to the development of resistance mechanisms to treatment. We demonstrate that the inhibition of polo-like kinase 1 (PLK1)...
Autores principales: | Eggermont, Carolien, Gutierrez, Gustavo J., De Grève, Jacques, Giron, Philippe |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177332/ https://www.ncbi.nlm.nih.gov/pubmed/37174055 http://dx.doi.org/10.3390/cancers15092589 |
Ejemplares similares
-
The EGFR-STYK1-FGF1 axis sustains functional drug tolerance to EGFR inhibitors in EGFR-mutant non-small cell lung cancer
por: Eggermont, Carolien, et al.
Publicado: (2022) -
Targeting USP13‐mediated drug tolerance increases the efficacy of EGFR inhibition of mutant EGFR in non‐small cell lung cancer
por: Giron, Philippe, et al.
Publicado: (2021) -
Targeting the tyrosine kinase inhibitor-resistant mutant EGFR pathway in lung cancer without targeting EGFR?
por: De Greve, Jacques, et al.
Publicado: (2020) -
Osimertinib – effective treatment of NSCLC with activating EGFR mutations after progression on EGFR tyrosine kinase inhibitors
por: Skrzypski, Marcin, et al.
Publicado: (2017) -
Clinical activity of the EGFR tyrosine kinase inhibitor osimertinib in EGFR-mutant glioblastoma
por: Makhlin, Igor, et al.
Publicado: (2019)