化学
细胞
单细胞分析
赫拉
癌细胞
癌症干细胞
癌症
表型
干细胞
计算生物学
癌症研究
细胞生物学
生物化学
生物
遗传学
基因
作者
Meijun Liu,Xing Wei,Chengxin Wu,Jinhui Liu,Yu-Jia Wei,Xuesheng Wang,Mingli Chen,Ting Yang,Jianhua Wang
标识
DOI:10.1021/acs.analchem.3c02934
摘要
Single cell phenotypic analysis is significant for clinical diagnosis, treatment, and prognosis of cancer. Accurate differentiation of cancer stem cell (CSC) subpopulations from a large number of cancer cells may become a cancer surveillance tool and provide important implications for the development of new CSC-targeted therapy strategies. Herein, we report a new approach based on dual-isotope inductively coupled plasma quadrupole mass spectrometry (ICP-QMS) for single cell phenotypic analysis. High-throughput single cell sampling was achieved by a spiral channel microfluidic chip for cell focusing and alignment, and single cell analysis was performed with time-resolved ICP-QMS by identifying the highly specific probes. This enables the monitoring of two surface protein markers (EpCAM and MUC1) of three cell types, i.e., HeLa, MCF-7, and HepG2, at single cell level. The analysis of breast cancer stem cells further confirmed its capability in distinguishing rare cell phenotypes. The present study provides promising possibilities for adopting ICP-QMS in biomedical investigations in terms of cell typing, stemness identification of tumor cells, and cell heterogeneity analysis.
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