Detection of circulating tumour cells in the breast cancer using CytoTrack system

Author:

Bogacz Anna12,Wolek Marlena3,Górska Aleksandra3,Leporowska Ewa4,Procyk Danuta4,Kolenda Piotr5,Litwiniuk Maria5,Uzar Izabela6,Gryszczyńska Agnieszka1,Łowicki Zdzisław1,Czerny Bogusław36

Affiliation:

1. Department of Pharmacology and Phytochemistry , Institute of Natural Fibres and Medicinal Plants , Kolejowa 2, 62-064 Plewiska , Poland

2. Department of Histocompatibility with Laboratory of Genetic Diagnostics , Regional Blood Center , Poznań , Poland

3. Department of Stem Cells and Regenerative Medicine , Institute of Natural Fibres and Medicinal Plants , Plewiska , Poland

4. Department of Laboratory Diagnostics , Greater Poland Cancer Centre , Poznań , Poland

5. Department of Chemotherapy , Greater Poland Cancer Centre , Poznań , Poland

6. Department of Pharmacology and Pharmacoeconomics , Pomeranian Medical University , Szczecin , Poland

Abstract

Summary Introduction: Plants are a rich source of healing substances. Cancer is a leading cause of death worldwide while breast cancer is the most common cancer among women. Circulating tumour cells (CTCs) are potential founder cells for metastasis. Therefore, their assessment may be used for monitoring of treatment as well as detecting cancer metastatis. Hence, it is suggested that the number of CTCs may be a valuable tumour biomarker during therapy. Objective: The purpose of this study was to detect CTCs in breast cancer and to validate the method of assessment of CTC count using CytoTrack CT11 technology. Methods: MCF-7 cells were sorted by a FACSARIA flow cytometer from blood samples derived from patients who have not been diagnosed with cancer. Identification and quantitative assessment of MCF-7 cells in blood samples were determined by flow sorting. Then, blood samples containing MCF-7 cells or without MCF-7 were scanned with the use of an automated fluorescence scanning microscope. Results: In in vitro model analysing the glass CytoDisc™ with stained MCF-7 cells, we noted the correlation between the amount of observed tumour cells and expected number of tumour cells. Moreover, coefficient of variation in case of the recovery rate of the assumed number of MCF-7 cells was 30%, 17%, 18% and 15%, respectively. Conclusion: Our study suggest that CTCs could be predictive factor in patients with metastatic cancer especially in breast cancer.

Publisher

Walter de Gruyter GmbH

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