Cargando…
The sodium channel-blocking antiepileptic drug phenytoin inhibits breast tumour growth and metastasis
BACKGROUND: Voltage-gated Na(+) channels (VGSCs) are heteromeric protein complexes containing pore-forming α subunits and smaller, non-pore-forming β subunits. VGSCs are classically expressed in electrically excitable cells, e.g. neurons. VGSCs are also expressed in tumour cells, including breast ca...
Autores principales: | Nelson, Michaela, Yang, Ming, Dowle, Adam A, Thomas, Jerry R, Brackenbury, William J |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320839/ https://www.ncbi.nlm.nih.gov/pubmed/25623198 http://dx.doi.org/10.1186/s12943-014-0277-x |
Ejemplares similares
-
The sodium channel β1 subunit mediates outgrowth of neurite-like processes on breast cancer cells and promotes tumour growth and metastasis
por: Nelson, Michaela, et al.
Publicado: (2014) -
Blocking channels to metastasis: targeting sodium transport in breast cancer
por: Brackenbury, William J., et al.
Publicado: (2023) -
Deep eutectic solvents for antiepileptic drug phenytoin solubilization: thermodynamic study
por: Shekaari, Hemayat, et al.
Publicado: (2021) -
Lacosamide and sodium channel‐blocking antiepileptic drug cross‐titration against levetiracetam background therapy
por: Baulac, M., et al.
Publicado: (2016) -
Therapeutic potential for phenytoin: targeting Na(v)1.5 sodium channels to reduce migration and invasion in metastatic breast cancer
por: Yang, Ming, et al.
Publicado: (2012)