1,3-Benzodioxole Derivatives Improve the Anti-Tumor Efficiency of Arsenicals

Arsenicals have been widely used in the treatment of cancers such as leukemia and other tumors. However, their side effects limit their clinical application. Stiripentol, a second-line adjunctive treatment for epilepsy with a good safety profile, inhibits microsomal cytochrome-P450-family enzymes to extend the retention time of co-administration. Inspired by the metabolism of stiripentol, the 1,3-benzodioxole responsible for the inhibition and its metabolic derivatives were conjugated with arsenical precursors. The fabricated arsenicals were eliminated much slower in mice and maintained an efficient concentration in the blood for a longer time than that of the arsenical precursors. They also performed better in anti-proliferation by inhibiting the thioredoxin system to induce oxidative stress, and concomitantly to initiate apoptosis in vitro and in vivo. The fabricated arsenicals reversed the hemogram of tumor-bearing mice to normal and eliminated the tumor without causing damage to any organs, exhibiting a good design strategy and pre-clinical application for leukemia and other tumors.

Automated summary

This study developed arsenicals by conjugating inhibitors with arsenical precursors, which effectively inhibited tumor growth and maintained a long-lasting presence in the body. These arsenicals eliminated tumors by inducing oxidative stress and apoptosis through the inhibition of the thioredoxin system, while restoring the hemogram to normal levels.