体内
循环肿瘤细胞
转移
CD44细胞
癌症研究
生物相容性
受体
配体(生物化学)
化学
癌症
生物医学工程
生物
细胞生物学
体外
医学
内科学
生物化学
生物技术
有机化学
作者
Xiaojie Wang,Yuan Ji,Jun Luo,Ying Sun,Tian‐Jiao Zhou,Yi Wang,Lei Xing,Hu‐Lin Jiang
出处
期刊:Small
[Wiley]
日期:2025-01-07
被引量:1
标识
DOI:10.1002/smll.202409036
摘要
Abstract Capturing circulating tumor cells (CTCs) in vivo from the bloodstream lessens tumor metastasis and recurrence risks. However, the absence of CTC receptors due to epithelial‐mesenchymal transition (EMT), the limited binding capacity of a single ligand, and the complexity of the blood flow environment significantly reduce the efficiency of CTC capture in vivo. Herein, a multivalent ligand‐decorated microsphere enrichment system (MLMES) is crafted that incorporates a capture column replete with an immunosorbent that precisely recognizes and binds the stably expressed cluster of differentiation 44 (CD44) and glucose transporter protein 1 (GLUT1) receptors present on the exterior of CTCs. As peripheral blood flows through the column, CTCs are efficiently captured, achieving an in vivo capture rate of up to 64.2%, the highest reported to date. Moreover, the MLMES demonstrates excellent biocompatibility, broad‐spectrum tumor cells capture, and storage stability. Importantly, it significantly eliminates a substantial quantity of CTCs from peripheral blood, reducing the risk of metastasis. This breakthrough method has broad clinical application potential in preventing tumor metastasis and recurrence, bringing new possibilities for improving cancer treatment.
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