International Journal of Molecular Sciences, Journal Year: 2025, Volume and Issue: 26(9), P. 4138 - 4138
Published: April 27, 2025
Chalcones, potential anticancer agents, have shown promise in the suppression of multidrug resistance due to inhibition drug efflux driven by certain adenosine triphosphate (ATP)-binding cassette (ABC) transporters. The gene and protein expression chosen ABC transporters (multidrug 1, ABCB1; resistance-associated ABCC1; breast cancer protein, ABCG2) human colorectal cells (COLO 205 COLO 320, which overexpress active ABCB1) was mainly studied this work under influence a novel synthetic acridine-based chalcone, 1C. While dropped just at 24 h, compound 1C selectively suppressed cell growth greatly lowered ABCB1 levels 320 24, 48, 72 h. It also reduced ABCC1 after 48 Molecular docking ATPase tests show that probably acts as an allosteric modulator ABCB1. galectin-1 (GAL1) Functional on revealed ABCC1/2 be major contributors both. Overall, transiently GAL1 while affecting important functional transporters, mostly lesser extent cells. 320’s absence points possible yet unknown interaction between
Language: Английский