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Flow Rate-Independent Multiscale Liquid Biopsy for Precision Oncology
[Image: see text] Immunoaffinity-based liquid biopsies of circulating tumor cells (CTCs) hold great promise for cancer management but typically suffer from low throughput, relative complexity, and postprocessing limitations. Here, we address these issues simultaneously by decoupling and independentl...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043932/ https://www.ncbi.nlm.nih.gov/pubmed/36802518 http://dx.doi.org/10.1021/acssensors.2c02577 |
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author | Wang, Jie Dallmann, Robert Lu, Renquan Yan, Jing Charmet, Jérôme |
author_facet | Wang, Jie Dallmann, Robert Lu, Renquan Yan, Jing Charmet, Jérôme |
author_sort | Wang, Jie |
collection | PubMed |
description | [Image: see text] Immunoaffinity-based liquid biopsies of circulating tumor cells (CTCs) hold great promise for cancer management but typically suffer from low throughput, relative complexity, and postprocessing limitations. Here, we address these issues simultaneously by decoupling and independently optimizing the nano-, micro-, and macro-scales of an enrichment device that is simple to fabricate and operate. Unlike other affinity-based devices, our scalable mesh approach enables optimum capture conditions at any flow rate, as demonstrated with constant capture efficiencies, above 75% between 50 and 200 μL min(–1). The device achieved 96% sensitivity and 100% specificity when used to detect CTCs in the blood of 79 cancer patients and 20 healthy controls. We demonstrate its postprocessing capacity with the identification of potential responders to immune checkpoint inhibition (ICI) therapy and the detection of HER2 positive breast cancer. The results compare well with other assays, including clinical standards. This suggests that our approach, which overcomes major limitations associated with affinity-based liquid biopsies, could help improve cancer management. |
format | Online Article Text |
id | pubmed-10043932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-100439322023-03-29 Flow Rate-Independent Multiscale Liquid Biopsy for Precision Oncology Wang, Jie Dallmann, Robert Lu, Renquan Yan, Jing Charmet, Jérôme ACS Sens [Image: see text] Immunoaffinity-based liquid biopsies of circulating tumor cells (CTCs) hold great promise for cancer management but typically suffer from low throughput, relative complexity, and postprocessing limitations. Here, we address these issues simultaneously by decoupling and independently optimizing the nano-, micro-, and macro-scales of an enrichment device that is simple to fabricate and operate. Unlike other affinity-based devices, our scalable mesh approach enables optimum capture conditions at any flow rate, as demonstrated with constant capture efficiencies, above 75% between 50 and 200 μL min(–1). The device achieved 96% sensitivity and 100% specificity when used to detect CTCs in the blood of 79 cancer patients and 20 healthy controls. We demonstrate its postprocessing capacity with the identification of potential responders to immune checkpoint inhibition (ICI) therapy and the detection of HER2 positive breast cancer. The results compare well with other assays, including clinical standards. This suggests that our approach, which overcomes major limitations associated with affinity-based liquid biopsies, could help improve cancer management. American Chemical Society 2023-02-20 /pmc/articles/PMC10043932/ /pubmed/36802518 http://dx.doi.org/10.1021/acssensors.2c02577 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Wang, Jie Dallmann, Robert Lu, Renquan Yan, Jing Charmet, Jérôme Flow Rate-Independent Multiscale Liquid Biopsy for Precision Oncology |
title | Flow Rate-Independent Multiscale Liquid Biopsy for
Precision Oncology |
title_full | Flow Rate-Independent Multiscale Liquid Biopsy for
Precision Oncology |
title_fullStr | Flow Rate-Independent Multiscale Liquid Biopsy for
Precision Oncology |
title_full_unstemmed | Flow Rate-Independent Multiscale Liquid Biopsy for
Precision Oncology |
title_short | Flow Rate-Independent Multiscale Liquid Biopsy for
Precision Oncology |
title_sort | flow rate-independent multiscale liquid biopsy for
precision oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043932/ https://www.ncbi.nlm.nih.gov/pubmed/36802518 http://dx.doi.org/10.1021/acssensors.2c02577 |
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