Yan Zuyun, Deng Youwen, Huang Liping, Zeng Jin, Wang Dong, Tong Zhaochen, Fan Qizhi, Tan Wei, Yan Jinpeng, Zang Xiaofang, Chen Shijie
Department of Spine Surgery, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410013, P. R. China.
Department of Cell Biology, School of Life Sciences, Central South University, Changsha, Hunan, 410017, P. R. China.
J Nanobiotechnology. 2025 Apr 9;23(1):286. doi: 10.1186/s12951-025-03253-w.
Achieving bone defect repair while preventing tumor recurrence after osteosarcoma surgery has consistently posed a clinical challenge. Local treatment with 3D-printed scaffolds loaded with chemotherapeutic drugs can exert certain effects in tumor inhibition and bone regeneration. However, the non-specific activation of chemotherapeutic drugs leads to high local toxic side effects and the formation of an immunosuppressive tumor microenvironment, thereby limiting their clinical application and therapeutic efficacy. To address this, we designed a Pt (IV) prodrug with low toxicity and minimal side effects, which releases Pt (II) in response to glutathione. This prodrug was grafted onto polydopamine (PDA) through an amidation reaction, resulting in a composite nanomaterial (PDA@Pt) that possesses both photothermal synergistic chemotherapy and immuno-oncological properties. Subsequently, we innovatively employed selective laser sintering technology to incorporate PDA@Pt into a poly (L-lactic acid)/bioactive glass matrix, successfully constructing a composite scaffold with dual anti-tumor and bone repair capabilities. The study revealed that the composite scaffold significantly inhibited the growth of osteosarcoma cells and activated the cGAS-STING pathway by inducing DNA damage, ultimately converting the 'cold tumor' into a 'hot tumor.' Additionally, the composite scaffold could induce osteogenic differentiation of bone marrow mesenchymal stem cells and exhibited excellent bone repair capabilities in vivo.
在骨肉瘤手术后实现骨缺损修复并防止肿瘤复发一直是一项临床挑战。用负载化疗药物的3D打印支架进行局部治疗可在肿瘤抑制和骨再生方面发挥一定作用。然而,化疗药物的非特异性激活会导致高局部毒性副作用并形成免疫抑制性肿瘤微环境,从而限制了它们的临床应用和治疗效果。为了解决这个问题,我们设计了一种低毒且副作用极小的铂(IV)前药,它能响应谷胱甘肽释放铂(II)。通过酰胺化反应将这种前药接枝到聚多巴胺(PDA)上,得到一种具有光热协同化疗和免疫肿瘤学特性的复合纳米材料(PDA@Pt)。随后,我们创新性地采用选择性激光烧结技术将PDA@Pt纳入聚(L-乳酸)/生物活性玻璃基质中,成功构建了一种具有双重抗肿瘤和骨修复能力的复合支架。研究表明,该复合支架显著抑制骨肉瘤细胞生长,并通过诱导DNA损伤激活cGAS-STING通路,最终将“冷肿瘤”转化为“热肿瘤”。此外,该复合支架可诱导骨髓间充质干细胞向成骨分化,并在体内表现出优异的骨修复能力。