血管生成
癌症研究
体外
内皮干细胞
体内
材料科学
化学
细胞生物学
生物化学
医学
生物
生物技术
作者
Zihao Sun,Yue Zhou,Lei Li,Chen Zhou,Wang Jia,Yang Liu,Xinran Cao,Shenge Su,Zhongpu Zhao,Mingming Zhen,Chunru Wang
标识
DOI:10.1016/j.scib.2023.06.031
摘要
Tumor vascular normalization (TVN) reverses abnormal tumor vasculatures, which could boost anti-cancer efficiency and especially increase drug intratumoral delivery. Endothelial cells play a vital role in angiogenesis, yet continuous modulating endothelial cell migration to improve TVN is ingenious but challenging. Here we propose a potential strategy for TVN based on inhibiting endothelial migration using nano-sized antioxidative fullerene nanoparticles (FNPs). We demonstrate that FNPs inhibit cell migration up on their anti-oxidation effects in vitro. The optimized alanine-modified gadofullerene (GFA) exhibits superior TVN ability and inhibits tumor growth in vivo. Mechanically, facilitated with the protein microarray, we confirm that GFA could suppress the focal adhesion pathway to restrain endothelial migration. Subsequently, remarkable anti-tumor efficacy of chemotherapy synergy was obtained, which benefited from a more normalized vascular network by GFA. Together, our study introduces the potential of FNPs as promising TVN boosters to consider in cancer nanomedicine design.
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