Precise Capture and Dynamic Release of Circulating Liver Cancer Cells with Dual-Histidine-Based Cell Imprinted Hydrogels.
Wenjing SunXin YouXinjia ZhaoXiaoyu ZhangChunhui YangFusheng ZhangJiaqi YuKaiguang YangJixia WangFangfang XuYongxin ChangBoxin QuXinmiao ZhaoYuxuan HeQi WangJinghua ChenGuangyan QingPublished in: Advanced materials (Deerfield Beach, Fla.) (2024)
Circulating tumor cells (CTCs) detection presents significant advantages in diagnosing liver cancer due to its noninvasiveness, real-time monitoring, and dynamic tracking. However, the clinical application of CTCs-based diagnosis is largely limited by the challenges of capturing low-abundance CTCs within a complex blood environment while ensuring them alive. Here, an ultrastrong ligand, l-histidine-l-histidine (HH), specifically targeting sialylated glycans on the surface of CTCs, is designed. Furthermore, HH is integrated into a cell-imprinted polymer, constructing a hydrogel with precise CTCs imprinting, high elasticity, satisfactory blood compatibility, and robust anti-interference capacities. These features endow the hydrogel with excellent capture efficiency (>95%) for CTCs in peripheral blood, as well as the ability to release CTCs controllably and alive. Clinical tests substantiate the accurate differentiation between liver cancer, cirrhosis, and healthy groups using this method. The remarkable diagnostic accuracy (94%), lossless release of CTCs, material reversibility, and cost-effectiveness ($6.68 per sample) make the HH-based hydrogel a potentially revolutionary technology for liver cancer diagnosis and single-cell analysis.
Keyphrases
- circulating tumor cells
- single cell
- drug delivery
- circulating tumor
- peripheral blood
- hyaluronic acid
- wound healing
- rna seq
- stem cells
- tissue engineering
- induced apoptosis
- high resolution
- high throughput
- signaling pathway
- cancer therapy
- oxidative stress
- mesenchymal stem cells
- cell proliferation
- cell cycle arrest
- wastewater treatment
- quantum dots
- sensitive detection
- real time pcr
- antibiotic resistance genes
- pi k akt