癌症研究
奥拉帕尼
化学
抗辐射性
DNA损伤
内化
聚ADP核糖聚合酶
微泡
合成致死
癌症
细胞生物学
细胞停滞
癌细胞
活性氧
PARP抑制剂
脂质体
吉西他滨
细胞凋亡
精密医学
生物物理学
DNA修复
放射治疗
肿瘤缺氧
个性化医疗
细胞
DNA
肿瘤微环境
磷脂酰丝氨酸
纳米技术
溶血磷脂酸
细胞培养
小发夹RNA
乙酰化
氧化应激
作者
Wanli Song,Chuanyi Zhao,Youqing Mai,Guangrong Zhang,Wenyue Kang,Xuanjun Zheng,Qingpeng Yuan,Zeyang Chen,Chengxun Zhong,Junbao Tang,Duoyi Fu,T. Zhai,Kai Ling,Hongyan Jiang
标识
DOI:10.1186/s12951-026-04027-8
摘要
Low-dose X-ray-activated radiodynamic therapy (RDT) is a promising strategy for precision oncology. However, its therapeutic efficacy is limited by tumor radioresistance and insufficient generation of reactive oxygen species (ROS). Here, we describe a biomimetic lutetium-coordinated black phosphorus nanosheet platform (BPNS@Lu3+/Lap-CMV) capable of initiating a tripartite synthetic lethality cascade upon low-dose irradiation. Through a single coordination strategy utilizing high atomic number (high-Z) Lu3+ ions, the nanoplatform simultaneously stabilizes the black phosphorus scaffold, functions as an efficient X-ray antenna, and integrates a pH-responsive gate for the controlled release of β-lapachone (Lap). Additionally, surface camouflage using cancer cell membrane vesicles (CMV) enables homologous tumor targeting and reduces clearance by the reticuloendothelial system. A multi-pathway therapeutic cascade is initiated upon exposure to low-dose X-ray. First, Lu3+-amplified RDT generates a burst of ROS. Second, tumor-overexpressed NAD(P)H: quinone oxidoreductase 1 (NQO1) bioactivates Lap, intensifying redox stress (GSH depletion and H2O2 overproduction) and promoting ferroptosis. Third, co-administration of the PARP inhibitor olaparib (Ola) functionally impairs PARP-mediated DNA repair, thereby converting RDT-induced DNA lesions into lethal damage and promoting apoptosis. Guided by its intrinsic computed tomography-mediated visibility, which revealed peak tumor accumulation at 12 h post-administration, the triple‑combination regimen achieved 85.5% tumor suppression in an orthotopic triple-negative breast cancer model without evident toxicity. This study presents a strategic framework for an intelligent nanoplatform capable of converting low-dose physical energy into biological cascades, thereby systematically disrupting parallel tumor defense mechanisms and broadening the therapeutic scope of radiotherapy.
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