Medical Oncology, Journal Year: 2025, Volume and Issue: 42(7)
Published: June 4, 2025
Language: Английский
Medical Oncology, Journal Year: 2025, Volume and Issue: 42(7)
Published: June 4, 2025
Language: Английский
Journal of Molecular Structure, Journal Year: 2025, Volume and Issue: unknown, P. 142044 - 142044
Published: March 1, 2025
Language: Английский
Citations
0ACS Pharmacology & Translational Science, Journal Year: 2025, Volume and Issue: unknown
Published: April 9, 2025
Preclinical research has traditionally utilized laboratory animals to elucidate the safety, tolerability, pharmacokinetics, and pharmacodynamics of new chemical entities prior human trials. The use animal models been pivotal in advancing scientific knowledge medical breakthroughs, contributing significantly our understanding complex biological processes diseases. However, many promising treatments that have demonstrated efficacy studies failed translate subjects during clinical Consequently, testing faces ethical concerns criticism regarding its predictive reliability for responses. This led development 3R principles (Replacement, Reduction, Refinement), introduced 1959, advocating alternative methods improved welfare research. Furthermore, regulatory frameworks recent legislation, such as 2022 FDA Modernisation Act, emphasize modern alternatives traditional testing. Emerging approaches, known 3Cs-cell culture, computer simulation, phase 0 trials-offer nonanimal solutions could accelerate drug address concerns, potentially rendering preclinical more humane efficient.
Language: Английский
Citations
0International 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
Citations
0Current Treatment Options in Oncology, Journal Year: 2025, Volume and Issue: unknown
Published: May 22, 2025
Language: Английский
Citations
0Medical Oncology, Journal Year: 2025, Volume and Issue: 42(7)
Published: June 4, 2025
Language: Английский
Citations
0