Sulfonamide inhibitors of beta-Catenin signaling as anticancerAgents with different output on c-Myc

01 Pubblicazione su rivista
Di Magno Laura, Di Pastena Fiorella, Puxeddu Michela, La Regina Giuseppe, Coluccia Antonio, Ciogli Alessia, Manetto Simone, Maroder Marella, Canettieri Gianluca, Silvestri Romano, Nalli Marianna
ISSN: 1860-7179

1The Wnt/beta-catenin pathway is often found deregulated incancer. The aberrant accumulation of beta-catenin in the cellnucleus results in the development of various malignancies. Specific drugs against this signaling pathway for clinical treat-ments have not been approved yet. Herein we report inhibitorsof beta-catenin signaling of potential therapeutic value asanticancer agents. Ethyl 4-((4-(trifluoromethyl)phenyl)sulfonamido)benzoate (compound 14) inhibits the effect onWnt reporter with an IC50value of 7.0 microM, significantly reducesc-MYC levels, inhibits HCT116 colon cancer cell growth (IC5020.2 microM), does not violate Lipinski and Veber rules, and showspredicted Caco-2 and MDCK cell permeability Papp>500 nm s-1.Compound 14 seems to have potential for the development ofnew anticancer therapies.

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