Sulfonamide inhibitors of beta-catenin signaling with different output on c-MYC as anticancer agents

Laura Di Magno, Fiorella Di Pastena, Michela Puxeddu, Giuseppe La Regina, Antonio Coluccia, Alessia Ciogli, Simone Manetto,Marella Maroder, Gianluca Canettieri, Romano Silvestri, Marianna Nalli. ChemMedChem 202015, 2264-2268.

The Wnt/b-catenin pathway is often found deregulated in cancer. The aberrant accumulation of b-catenin in the cell nucleus results in the development of various malignancies. Specific drugs against this signaling pathway for clinical treatments have not been approved yet. Here we report inhibitors of b-catenin signaling of potential therapeutic value as anticancer agents. Compound 14 inhibits the effect on Wnt reporter with IC50 of 7.0 μM, significantly reduces c-MYC levels, inhibits HCT116 colon cancer cell growth with IC50 of 20.2 mM, does not violate the Lipinski and Veber rules and shows predicted Caco-2 and MDCK cell permeability Papp >500 nm/s. Compound 14 seems to have potential for the development of new anticancer therapies

Leave a Reply

Your email address will not be published. Required fields are marked *

DDSC


Department of Drug Chemistry and Technologies
Sapienza University of Rome
Laboratory affiliated to Istituto Pasteur Italia
Fondazione Cenci Bolognetti
Piazzale Aldo Moro 5, I-00185 Roma, Italy
Phone: +39 06 4991 3800 – Fax: +39 06 49913993
Email: info@romanosilvestri.it