Development of PowerMag System II for Isolation of Circulating Tumor Cells with Improved Purity

Cheng Rou Ho, Hui Ju Tsai, Jin Ru Wang, Chia Te Wang, Chiuan Chian Chiou, Ju Chien Cheng, Sum Fu Chiang*, Ching Ping Tseng*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

Abstract

Background/Objectives: The PowerMag system (PM) is a platform for the isolation of circulating tumor cells (CTCs) by the depletion of CD45+-leukocytes. However, an EpCAMCD45 cell population is present in large numbers in the cell filtrates collected by PM. This lowers the purity of the CTCs and negatively impacts their molecular characterization. The aims of this study are to characterize the cellular properties of the EpCAMCD45 cells and to upgrade the system to improve CTC purity. Methods: A real-time RT-PCR assay, Liu’s stain analysis, and Annexin V (AnxV) binding assay were used to define the cellular properties of the EpCAMCD45 cells. An upgraded system was developed to remove the EpCAMCD45 cells and improve the CTC purity. Clinical blood samples were used to evaluate the performance of the system. Results: The EpCAMCD45 cells were defined as apoptotic cells, which displayed apoptotic body-like morphology and elicited AnxV binding activity. AnxV beads developed in-house can effectively bind and remove EpCAMCD45 cells from the cell filtrates. An improved generation of a CTCs isolation platform, designated as PM II, was developed by integration of AnxV beads into the workflow to remove the apoptotic cells. PM II recovered CTCs with improved CTC purity by effective removal of the background apoptotic cells. The improved performance of PM II allowed for direct profiling of cancer-related gene mutations by next-generation sequencing without cell picking and further purification. Conclusions: PM II holds great promise as a platform for isolating CTCs with improved purity and for exploring its application in cancer diagnosis and monitoring in a clinical setting.

Original languageEnglish
Article number431
JournalBiomedicines
Volume13
Issue number2
DOIs
StatePublished - 11 02 2025

Bibliographical note

Publisher Copyright:
© 2025 by the authors.

Keywords

  • annexin V
  • apoptosis
  • cancer
  • circulating tumor cells

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