化学
声动力疗法
白藜芦醇
癌症研究
乳腺癌
卡帕
转录因子
药理学
癌症
细胞凋亡
生物化学
医学
内科学
基因
语言学
哲学
作者
Yuanyuan Li,Ming Sun,Jie Yu,Wei Jiang,Wei Tian,Xin Chen,Silong Zhang,Huan He
标识
DOI:10.1021/acs.jmedchem.2c01992
摘要
Sonodynamic therapy (SDT) has been recognized as a spatial–temporal and noninvasive modality for the treatment of deep-seated tumors. However, current sonosensitizers suffer from low sonodynamic efficacy. Herein, we reported the design of nuclear factor kappa B (NF-κB) targeting sonosensitizers (TR1, TR2, and TR3) by integrating a resveratrol motif into a conjugated electron donor–acceptor (triphenylamine benzothiazole) skeleton. Among these sonosensitizers, TR2 with two resveratrol units in one molecule was the most potent for inhibiting NF-κB signaling. Owing to the synergy of high sonodynamic efficacy and NF-κB activation inhibition, TR2 displayed a remarkable sonocytotoxicity to MCF-7 breast cancer cells. Xenograft mice studies demonstrated that TR2 had excellent anticancer potency and biosafety. This study thus opens up a new avenue for the development of efficient organic sonosensitizers for cancer ablation.
科研通智能强力驱动
Strongly Powered by AbleSci AI