循环肿瘤细胞
单细胞测序
单细胞分析
液体活检
计算生物学
转录组
细胞
生物
癌细胞
癌症
大规模并行测序
乳腺癌
计算机科学
转移
癌症研究
DNA测序
基因
基因表达
表型
遗传学
外显子组测序
作者
Yu-Heng Cheng,Yu‐Chih Chen,Eric Lin,Riley Brien,Seungwon Jung,Chen Yuting,Wonchoel Lee,Zhijian Hao,Saswat Sahoo,Hyun Min Kang,Jason Cong,Monika L. Burness,Sunitha Nagrath,Max S. Wicha,Euisik Yoon
标识
DOI:10.1038/s41467-019-10122-2
摘要
Abstract Molecular analysis of circulating tumor cells (CTCs) at single-cell resolution offers great promise for cancer diagnostics and therapeutics from simple liquid biopsy. Recent development of massively parallel single-cell RNA-sequencing (scRNA-seq) provides a powerful method to resolve the cellular heterogeneity from gene expression and pathway regulation analysis. However, the scarcity of CTCs and the massive contamination of blood cells limit the utility of currently available technologies. Here, we present Hydro-Seq, a scalable hydrodynamic scRNA-seq barcoding technique, for high-throughput CTC analysis. High cell-capture efficiency and contamination removal capability of Hydro-Seq enables successful scRNA-seq of 666 CTCs from 21 breast cancer patient samples at high throughput. We identify breast cancer drug targets for hormone and targeted therapies and tracked individual cells that express markers of cancer stem cells (CSCs) as well as of epithelial/mesenchymal cell state transitions. Transcriptome analysis of these cells provides insights into monitoring target therapeutics and processes underlying tumor metastasis.
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