Discovery of Novel Anti-Breast-Cancer Inhibitors by Synergistically Antagonizing Microtubule Polymerization and Aryl Hydrocarbon Receptor Expression

A series of unreported dual-receptor inhibitors targeting both the tubulin colchicine site and AhR were designed and synthesized, and their anti-breast-cancer activities were evaluated. Compound 12 showed the strongest activity with an IC50 of 0.9 nM in MCF-7 cell lines. Besides, 12 could significantly inhibit cancer growth in MCF-7 xenograft tumor models with no obvious toxic effects and was more effective than the positive control (combretastatin A-4). With the in-depth study, it was found that 12 could induce apoptosis in breast cancer cells by making arrest in G2/M phase, depolarizing mitochondria and inducing intracellular reactive oxygen generation. This evident anticancer effect and the ability to inhibit cell migration were attributed to the synergistic antagonism of 12 on tubulin and AhR. In general, 12 was worthy of further research as an effective and safe anti-breast-cancer drug.

Automated summary

Compound 12, a novel dual-receptor inhibitor targeting both tubulin and AhR, showed strong anti-breast-cancer activity with potent inhibition of tumor growth in cell lines and xenograft models, as well as inducing apoptosis in breast cancer cells. Its ability to synergistically antagonize tubulin and AhR makes it a promising candidate for further development as an effective and safe anti-breast-cancer drug.