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The SRC family kinase inhibitor NXP900 demonstrates potent antitumor activity in squamous cell carcinomas.

Authors :
Dash, Sweta
Hanson, Sabrina
King, Ben
Nyswaner, Katherine
Foss, Kelcie
Tesi, Noelle
Harvey, Mungo J. B.
Navarro-Marchal, Saúl A.
Woods, Allison
Poradosu, Enrique
Unciti-Broceta, Asier
Carragher, Neil O.
Brognard, John
Source :
Journal of Biological Chemistry. Sep2024, Vol. 300 Issue 9, p1-9. 9p.
Publication Year :
2024

Abstract

NXP900 is a selective and potent SRC family kinase (SFK) inhibitor, currently being dosed in a phase 1 clinical trial, that locks SRC in the “closed” conformation, thereby inhibiting both kinase-dependent catalytic activity and kinaseindependent functions. In contrast, several multi-targeted kinase inhibitors that inhibit SRC, including dasatinib and bosutinib, bind their target in the active “open” conformation, allowing SRC and other SFKs to act as a scaffold to promote tumorigenesis through non-catalytic functions. NXP900 exhibits a unique target selectivity profile with sub-nanomolar activity against SFK members over other kinases. This results in highly potent and specific SFK pathway inhibition. Here, we demonstrate that esophageal squamous cell carcinomas and head and neck squamous cell carcinomas are exquisitely sensitive to NXP900 treatment in cell culture and in vivo, and we identify a patient population that could benefit from treatment with NXP900. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219258
Volume :
300
Issue :
9
Database :
Academic Search Index
Journal :
Journal of Biological Chemistry
Publication Type :
Academic Journal
Accession number :
180141726
Full Text :
https://doi.org/10.1016/j.jbc.2024.107615