School of Pharmacy, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China.
ACS Appl Mater Interfaces. 2022 Jun 1;14(21):24089-24101. doi: 10.1021/acsami.2c00574. Epub 2022 May 19.
Single therapy for tumor therapy always exerts limited ability for the constraints on the reaction condition and the unavoidable multidrug resistance, which seriously influences the therapy effect in the clinic. Herein, a combination treatment nanosystem (MP@PI) based on chemodynamic therapy (CDT) and photothermal therapy (PTT) is constructed for triggering ferroptosis/pyroptosis, which is the metal-organic framework (MOF) modified with polydopamine (PDA) and IR820 to loaded with piperlongumine (PL). The MOF and PL respectively served as the iron source and HO source, performing chemodynamic therapy (CDT) for eliciting ferroptosis. Meanwhile the iron source induces pyroptosis in tumor cells. PDA is not only pH responsive to release PL but also CDT-assisted which due to PDA consumes the glutathione to decrease the expression of glutathione peroxide 4. The photosensitizer IR820 exerts photothermal effects under near-infrared light and further facilitates the ferroptosis/pyroptosis. In addation, the MP@PI nanoplatform evokes the immune response in vivo and enhances the antitumor effects further. Overall, MP@PI is a kind of promising cancer therapy strategy through CDT and PTT combination, inducing ferroptosis and pyroptosis.
单一的肿瘤治疗方法总是受到反应条件的限制和不可避免的多药耐药性的限制,这严重影响了临床治疗效果。在此,构建了一种基于化学动力学治疗(CDT)和光热治疗(PTT)的联合治疗纳米系统(MP@PI),用于触发铁死亡/细胞焦亡,该系统是用聚多巴胺(PDA)和 IR820 修饰的金属-有机骨架(MOF)来负载胡椒碱(PL)。MOF 和 PL 分别作为铁源和 HO 源,进行化学动力学治疗(CDT)以引发铁死亡。同时,铁源诱导肿瘤细胞发生细胞焦亡。PDA 不仅可以响应 pH 值释放 PL,还可以通过 CDT 辅助,因为 PDA 消耗谷胱甘肽,降低谷胱甘肽过氧化物酶 4 的表达。光敏剂 IR820 在近红外光下产生光热效应,进一步促进铁死亡/细胞焦亡。此外,MP@PI 纳米平台在体内引发免疫反应,进一步增强抗肿瘤效果。总之,MP@PI 通过 CDT 和 PTT 的联合应用是一种很有前途的癌症治疗策略,可诱导铁死亡和细胞焦亡。