Citation:
PANG Shu-Yun, XU Shu, XU Zhao-Luo, CHU Ya-Nan, MA Xue-Ping, WU Hai-Ping, ZOU Bing-Jie, ZHOU Guo-Hua. Quality Evaluation of Capture and Single-cell Isolation of Circulating Tumor Cell Clusters for Single-cell Ribonucleic Acid Analysis[J]. Chinese Journal of Analytical Chemistry,
;2023, 51(4): 513-520.
doi:
10.19756/j.issn.0253-3820.221526
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Single-cell ribonucleic acid (RNA) analysis is necessary to investigate the biological effects of circulating tumor cell clusters (CTC clusters). To achieve the most efficient results in single-cell analysis of CTC clusters, the integrity of the CTC cluster and the high quality of the intracellular RNA should be maintained after the capture and single-cell isolation. So, three house gene was quantitated in single cells for RNA quality control by single-cell RNA sequencing method, and the CTC cluster's lateral diameter for evaluating the CTC cluster's integrity were used to evaluate the quality of CTC cluster capture and single-cell isolation process. Trypsin-EDTA and non-enzymatic cell dissociation solution (NECDS) were used to isolate single cells in CTC clusters, followed by the investigation of intracellular RNA quality. The CTC cluster recovery of negative enrichment, positive enrichment and membrane filtration, and single-cell RNA integrity after enrichment were investigated. The results indicated that the NECDS isolated single cells from CTC clusters rapidly without affecting the intracellular RNA. Besides, it was found that rotational incubation and treatments of red blood cell lysate disrupted the integrity of CTC clusters, therefore, these operations were not the best way for single-cell RNA analysis of CTC clusters. The positive enrichment with simplified process achieved a high recovery without affecting the quality of intracellular RNA. Single-cell RNA analysis of CTC clusters required gentle capture and single-cell isolation process. The present study here provided an efficient sample preparation strategy for single-cell analysis of CTC clusters.
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