Cargando…
Differential protein stability of EGFR mutants determines responsiveness to tyrosine kinase inhibitors
Non-small cell lung cancer (NSCLC) patients carrying specific EGFR kinase activating mutations (L858R, delE746-A750) respond well to tyrosine kinase inhibitors (TKIs). However, drug resistance develops within a year. In about 50% of such patients, acquired drug resistance is attributed to the enrich...
Autores principales: | Ray, Paramita, Tan, Yee Sun, Somnay, Vishal, Mehta, Ranjit, Sitto, Merna, Ahsan, Aarif, Nyati, Shyam, Naughton, John P., Bridges, Alexander, Zhao, Lili, Rehemtulla, Alnawaz, Lawrence, Theodore S., Ray, Dipankar, Nyati, Mukesh K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356576/ https://www.ncbi.nlm.nih.gov/pubmed/27612423 http://dx.doi.org/10.18632/oncotarget.11860 |
Ejemplares similares
-
Budding uninhibited by benzimidazoles-1 (BUB1) regulates EGFR signaling by reducing EGFR internalization
por: Nyati, Shyam, et al.
Publicado: (2023) -
Inducing Oncoprotein Degradation to Improve Targeted Cancer Therapy()
por: Ray, Dipankar, et al.
Publicado: (2015) -
TGFBR2 mediated phosphorylation of BUB1 at Ser-318 is required for transforming growth factor-β signaling
por: Nyati, Shyam, et al.
Publicado: (2020) -
Disruptin, a cell-penetrating peptide degrader of EGFR: Cell-Penetrating Peptide in Cancer Therapy
por: Mehta, Ranjit K., et al.
Publicado: (2021) -
Membrane Transition Temperature Determines Cisplatin Response
por: Raghunathan, Krishnan, et al.
Publicado: (2015)