Zhang Wei, Ran Yijun, Yang Mi, Hu Yaqin, Wang Zhigang, Cao Yang, Ran Haitao
Department of Ultrasound, Second Affiliated Hospital of Chongqing Medical University & Chongqing Key Laboratory of Ultrasound Molecular Imaging, Chongqing, 400010, China.
Department of Radiology, Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China.
Adv Healthc Mater. 2024 Dec;13(31):e2402349. doi: 10.1002/adhm.202402349. Epub 2024 Sep 2.
Amplifying oxidative stress to disrupt intracellular redox homeostasis can accelerate tumor cell death. In this work, an oxidative stress amplifier (PP@T) is prepared for enhanced tumor oxidation therapy to reduce tumor growth and metastases. The nano-amplifier has been successfully constructed by embedding MTH1 inhibitor (TH588) in the PDA-coated porphyrin metal-organic framework PCN-224. The controllable-released TH588 is demonstrated from pores can hinder MTH1-mediated damage-repairing process by preventing the hydrolysis of 8-oxo-dG, thereby amplifying oxidative stress and exacerbating the oxidative DNA damage induced by the sonodynamic therapy of PP@T under ultrasound irradiation. Furthermore, PP@T can effectively induce immunogenic cell death to trigger systemic anti-tumor immune response. When administered in combination with immune checkpoint blockade, PP@T not only impedes the progression of the primary tumor but also achieves obvious antimetastasis in breast cancer murine models, including orthotopic and artificial whole-body metastasis models. Furthermore, the nanoplatform also provides photoacoustic imaging for in vivo treatment guidance. In conclusion, by amplifying oxidative stress and reactive oxygen species sensitized immunotherapy, this image-guided nanosystem shows potential for highly specific, effective combined therapy against tumor cells with negligible side-effects to normal cells which will provide a new insight for precise tumor treatment.
增强氧化应激以破坏细胞内氧化还原稳态可加速肿瘤细胞死亡。在这项工作中,制备了一种氧化应激放大器(PP@T)用于增强肿瘤氧化治疗,以减少肿瘤生长和转移。通过将MTH1抑制剂(TH588)嵌入聚多巴胺包覆的卟啉金属有机框架PCN - 224中,成功构建了这种纳米放大器。从孔中释放的可控TH588可通过阻止8 - 氧代脱氧鸟苷的水解来阻碍MTH1介导的损伤修复过程,从而增强氧化应激并加剧PP@T在超声照射下的声动力疗法诱导的氧化性DNA损伤。此外,PP@T可有效诱导免疫原性细胞死亡以触发全身抗肿瘤免疫反应。当与免疫检查点阻断联合使用时,PP@T不仅能阻碍原发性肿瘤的进展,还能在乳腺癌小鼠模型(包括原位和人工全身转移模型)中实现明显的抗转移作用。此外,该纳米平台还提供光声成像用于体内治疗指导。总之,通过增强氧化应激和活性氧致敏免疫疗法,这种图像引导的纳米系统显示出对肿瘤细胞进行高度特异性、有效联合治疗的潜力,对正常细胞的副作用可忽略不计,这将为精确肿瘤治疗提供新的见解。