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Accurate isolation and detection of circulating tumor cells using enrichment-free multiparametric high resolution imaging
INTRODUCTION: The reliable and accurate detection of rare circulating tumor cells (CTCs) from cancer patient blood samples promises advantages in both research and clinical applications. Numerous CTC detection methods have been explored that rely on either the physical properties of CTCs such as den...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083432/ https://www.ncbi.nlm.nih.gov/pubmed/37051527 http://dx.doi.org/10.3389/fonc.2023.1141228 |
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author | Yeo, Dannel Kao, Steven Gupta, Ruta Wahlroos, Sara Bastian, Althea Strauss, Heidi Klemm, Vera Shrestha, Prajwol Ramirez, Arturo B. Costandy, Lillian Huston, Ryan Gardner, Brady S. Grimison, Peter Clark, Jonathan R. Rasko, John E. J. |
author_facet | Yeo, Dannel Kao, Steven Gupta, Ruta Wahlroos, Sara Bastian, Althea Strauss, Heidi Klemm, Vera Shrestha, Prajwol Ramirez, Arturo B. Costandy, Lillian Huston, Ryan Gardner, Brady S. Grimison, Peter Clark, Jonathan R. Rasko, John E. J. |
author_sort | Yeo, Dannel |
collection | PubMed |
description | INTRODUCTION: The reliable and accurate detection of rare circulating tumor cells (CTCs) from cancer patient blood samples promises advantages in both research and clinical applications. Numerous CTC detection methods have been explored that rely on either the physical properties of CTCs such as density, size, charge, and/or their antigen expression profiles. Multiple factors can influence CTC recovery including blood processing method and time to processing. This study aimed to examine the accuracy and sensitivity of an enrichment-free method of isolating leukocytes (AccuCyte(®) system) followed by immunofluorescence staining and high-resolution imaging (CyteFinder(®) instrument) to detect CTCs. METHOD: Healthy human blood samples, spiked with cancer cells from cancer cell lines, as well as blood samples obtained from 4 subjects diagnosed with cancer (2 pancreatic, 1 thyroid, and 1 small cell lung) were processed using the AccuCyte-CyteFinder system to assess recovery rate, accuracy, and reliability over a range of processing times. RESULTS: The AccuCyte-CyteFinder system was highly accurate (95.0%) at identifying cancer cells in spiked-in samples (in 7.5 mL of blood), even at low spiked-in numbers of 5 cells with high sensitivity (90%). The AccuCyte-CyteFinder recovery rate (90.9%) was significantly higher compared to recovery rates obtained by density gradient centrifugation (20.0%) and red blood cell lysis (52.0%). Reliable and comparable recovery was observed in spiked-in samples and in clinical blood samples processed up to 72 hours post-collection. Reviewer analysis of images from spiked-in and clinical samples resulted in high concordance (R-squared value of 0.998 and 0.984 respectively). DISCUSSION: The AccuCyte-CyteFinder system is as an accurate, sensitive, and clinically practical method to detect and enumerate cancer cells. This system addresses some of the practical logistical challenges in incorporating CTCs as part of routine clinical care. This could facilitate the clinical use of CTCs in guiding precision, personalized medicine. |
format | Online Article Text |
id | pubmed-10083432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100834322023-04-11 Accurate isolation and detection of circulating tumor cells using enrichment-free multiparametric high resolution imaging Yeo, Dannel Kao, Steven Gupta, Ruta Wahlroos, Sara Bastian, Althea Strauss, Heidi Klemm, Vera Shrestha, Prajwol Ramirez, Arturo B. Costandy, Lillian Huston, Ryan Gardner, Brady S. Grimison, Peter Clark, Jonathan R. Rasko, John E. J. Front Oncol Oncology INTRODUCTION: The reliable and accurate detection of rare circulating tumor cells (CTCs) from cancer patient blood samples promises advantages in both research and clinical applications. Numerous CTC detection methods have been explored that rely on either the physical properties of CTCs such as density, size, charge, and/or their antigen expression profiles. Multiple factors can influence CTC recovery including blood processing method and time to processing. This study aimed to examine the accuracy and sensitivity of an enrichment-free method of isolating leukocytes (AccuCyte(®) system) followed by immunofluorescence staining and high-resolution imaging (CyteFinder(®) instrument) to detect CTCs. METHOD: Healthy human blood samples, spiked with cancer cells from cancer cell lines, as well as blood samples obtained from 4 subjects diagnosed with cancer (2 pancreatic, 1 thyroid, and 1 small cell lung) were processed using the AccuCyte-CyteFinder system to assess recovery rate, accuracy, and reliability over a range of processing times. RESULTS: The AccuCyte-CyteFinder system was highly accurate (95.0%) at identifying cancer cells in spiked-in samples (in 7.5 mL of blood), even at low spiked-in numbers of 5 cells with high sensitivity (90%). The AccuCyte-CyteFinder recovery rate (90.9%) was significantly higher compared to recovery rates obtained by density gradient centrifugation (20.0%) and red blood cell lysis (52.0%). Reliable and comparable recovery was observed in spiked-in samples and in clinical blood samples processed up to 72 hours post-collection. Reviewer analysis of images from spiked-in and clinical samples resulted in high concordance (R-squared value of 0.998 and 0.984 respectively). DISCUSSION: The AccuCyte-CyteFinder system is as an accurate, sensitive, and clinically practical method to detect and enumerate cancer cells. This system addresses some of the practical logistical challenges in incorporating CTCs as part of routine clinical care. This could facilitate the clinical use of CTCs in guiding precision, personalized medicine. Frontiers Media S.A. 2023-03-27 /pmc/articles/PMC10083432/ /pubmed/37051527 http://dx.doi.org/10.3389/fonc.2023.1141228 Text en Copyright © 2023 Yeo, Kao, Gupta, Wahlroos, Bastian, Strauss, Klemm, Shrestha, Ramirez, Costandy, Huston, Gardner, Grimison, Clark and Rasko https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Yeo, Dannel Kao, Steven Gupta, Ruta Wahlroos, Sara Bastian, Althea Strauss, Heidi Klemm, Vera Shrestha, Prajwol Ramirez, Arturo B. Costandy, Lillian Huston, Ryan Gardner, Brady S. Grimison, Peter Clark, Jonathan R. Rasko, John E. J. Accurate isolation and detection of circulating tumor cells using enrichment-free multiparametric high resolution imaging |
title | Accurate isolation and detection of circulating tumor cells using enrichment-free multiparametric high resolution imaging |
title_full | Accurate isolation and detection of circulating tumor cells using enrichment-free multiparametric high resolution imaging |
title_fullStr | Accurate isolation and detection of circulating tumor cells using enrichment-free multiparametric high resolution imaging |
title_full_unstemmed | Accurate isolation and detection of circulating tumor cells using enrichment-free multiparametric high resolution imaging |
title_short | Accurate isolation and detection of circulating tumor cells using enrichment-free multiparametric high resolution imaging |
title_sort | accurate isolation and detection of circulating tumor cells using enrichment-free multiparametric high resolution imaging |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10083432/ https://www.ncbi.nlm.nih.gov/pubmed/37051527 http://dx.doi.org/10.3389/fonc.2023.1141228 |
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