脚手架
骨肉瘤
材料科学
体内
PI3K/AKT/mTOR通路
生物医学工程
癌症研究
体外
细胞凋亡
化学
医学
生物化学
生物
生物技术
作者
Yupu Lu,Aobo Liu,Siqi Jin,Jiabao Dai,Yameng Yu,Peng Wen,Yufeng Zheng,Dandan Xia
标识
DOI:10.1002/adma.202410589
摘要
Abstract Postoperative therapies for osteosarcoma present substantial challenges due to tumor recurrence and extensive bone defects. To tackle these challenges, laser powder bed fusion is utilized to fabricate biodegradable Zn‐Li porous scaffolds that supress tumors and promote osteogenesis. After the structure design and composition selection, the Zn‐0.8Li porous scaffold with Gyroid unit optimally balances the co‐release of Zn 2+ and Li + during degradation, resulting in favorable antitumor and osteogenic effects. In vitro, the Zn‐0.8Li scaffold significantly inhibits osteosarcoma progression by suppressing tumor cell proliferation, promoting apoptosis, alleviating migration, and simultaneously promotes osteogenic differentiation through the enhanced expression of osteogenic markers. In vivo, the Zn‐0.8Li scaffold inhibits the malignant osteosarcoma behavior and facilitates bone regeneration in areas with bone defects. Transcriptomic analysis further reveals that the simultaneous release of Zn 2+ and Li + from the biodegradable Zn‐0.8Li scaffold contributes to anti‐osteosarcoma activity by downregulating PI3K/Akt signaling pathways. Taken together, the Zn‐0.8Li porous scaffold fabricated using laser powder bed fusion with enhanced antitumor and osteogenic properties is a promising alternative for the postoperative management of osteosarcoma.
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