Cargando…
Mechanistic Validation of a Clinical Lead Stapled Peptide that Reactivates p53 by Dual HDM2 and HDMX Targeting
Hydrocarbon-stapled peptides that display key residues of the p53 transactivation domain have emerged as bona fide clinical candidates for reactivating the tumor suppression function of p53 in cancer by dual targeting of the negative regulators HDM2 and HDMX. A recent study questioned the mechanisti...
Autores principales: | Wachter, Franziska, Morgan, Ann M., Godes, Marina, Mourtada, Rida, Bird, Gregory H., Walensky, Loren D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386833/ https://www.ncbi.nlm.nih.gov/pubmed/27721413 http://dx.doi.org/10.1038/onc.2016.361 |
Ejemplares similares
-
Alterations in gene expression and sensitivity to genotoxic
stress following HdmX or Hdm2 knockdown in human tumor cells harboring
wild-type p53
por: Heminger, Katherine, et al.
Publicado: (2009) -
Understanding the interaction of 14‐3‐3 proteins with hDMX and hDM2: a structural and biophysical study
por: Srdanović, Sonja, et al.
Publicado: (2022) -
Biophysical Determinants for Cellular Uptake of Hydrocarbon-Stapled Peptide Helices
por: Bird, Gregory H., et al.
Publicado: (2016) -
Design of Stapled Antimicrobial Peptides that Overcome Antibiotic
Resistance and In Vivo Toxicity
por: Mourtada, Rida, et al.
Publicado: (2019) -
Hydrocarbon-Stapled Peptides:
Principles, Practice,
and Progress: Miniperspective
por: Walensky, Loren D., et al.
Publicado: (2014)