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Beyond Circulating Tumor Cell Enumeration: Cell-Based Liquid Biopsy to Assess Protein Biomarkers and Cancer Genomics Using the RareCyte(®) Platform

The practice of medicine has steadily employed less invasive methods to obtain information derived from the tumor to guide clinical management of patients. Liquid biopsy—the sampling of blood—is a non-invasive method for generating information previously only available from tissue biopsies of the tu...

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Autores principales: Kaldjian, Eric P., Ramirez, Arturo B., Costandy, Lillian, Ericson, Nolan G., Malkawi, Walla I., George, Thaddeus C., Kasi, Pashtoon Murtaza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927801/
https://www.ncbi.nlm.nih.gov/pubmed/35308236
http://dx.doi.org/10.3389/fphar.2022.835727
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author Kaldjian, Eric P.
Ramirez, Arturo B.
Costandy, Lillian
Ericson, Nolan G.
Malkawi, Walla I.
George, Thaddeus C.
Kasi, Pashtoon Murtaza
author_facet Kaldjian, Eric P.
Ramirez, Arturo B.
Costandy, Lillian
Ericson, Nolan G.
Malkawi, Walla I.
George, Thaddeus C.
Kasi, Pashtoon Murtaza
author_sort Kaldjian, Eric P.
collection PubMed
description The practice of medicine has steadily employed less invasive methods to obtain information derived from the tumor to guide clinical management of patients. Liquid biopsy—the sampling of blood—is a non-invasive method for generating information previously only available from tissue biopsies of the tumor mass. Analysis of fragmented circulating tumor DNA in the plasma is clinically used to identify actionable mutations and detect residual or recurrent disease. Plasma analysis cannot, however, assess cancer phenotypes, including the expression of drug targets and protein biomarkers. Circulating tumor cells (CTCs) are intact cancer cells that have entered the blood that have the potential for distant metastasis. While enumeration of CTCs is prognostic of outcome, recently developed technology allows for the interrogation of protein biomarkers on CTCs that could be predictive of response. Furthermore, since CTCs contain intact whole cancer genomes, isolating viable CTCs detected during therapy could provide a rational approach to assessing mutational profiles of resistance. Identification, characterization and molecular analysis of CTCs together will advance the capacity of liquid biopsy to meet the requirements of twenty-first century medicine.
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spelling pubmed-89278012022-03-18 Beyond Circulating Tumor Cell Enumeration: Cell-Based Liquid Biopsy to Assess Protein Biomarkers and Cancer Genomics Using the RareCyte(®) Platform Kaldjian, Eric P. Ramirez, Arturo B. Costandy, Lillian Ericson, Nolan G. Malkawi, Walla I. George, Thaddeus C. Kasi, Pashtoon Murtaza Front Pharmacol Pharmacology The practice of medicine has steadily employed less invasive methods to obtain information derived from the tumor to guide clinical management of patients. Liquid biopsy—the sampling of blood—is a non-invasive method for generating information previously only available from tissue biopsies of the tumor mass. Analysis of fragmented circulating tumor DNA in the plasma is clinically used to identify actionable mutations and detect residual or recurrent disease. Plasma analysis cannot, however, assess cancer phenotypes, including the expression of drug targets and protein biomarkers. Circulating tumor cells (CTCs) are intact cancer cells that have entered the blood that have the potential for distant metastasis. While enumeration of CTCs is prognostic of outcome, recently developed technology allows for the interrogation of protein biomarkers on CTCs that could be predictive of response. Furthermore, since CTCs contain intact whole cancer genomes, isolating viable CTCs detected during therapy could provide a rational approach to assessing mutational profiles of resistance. Identification, characterization and molecular analysis of CTCs together will advance the capacity of liquid biopsy to meet the requirements of twenty-first century medicine. Frontiers Media S.A. 2022-03-03 /pmc/articles/PMC8927801/ /pubmed/35308236 http://dx.doi.org/10.3389/fphar.2022.835727 Text en Copyright © 2022 Kaldjian, Ramirez, Costandy, Ericson, Malkawi, George and Kasi. 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 Pharmacology
Kaldjian, Eric P.
Ramirez, Arturo B.
Costandy, Lillian
Ericson, Nolan G.
Malkawi, Walla I.
George, Thaddeus C.
Kasi, Pashtoon Murtaza
Beyond Circulating Tumor Cell Enumeration: Cell-Based Liquid Biopsy to Assess Protein Biomarkers and Cancer Genomics Using the RareCyte(®) Platform
title Beyond Circulating Tumor Cell Enumeration: Cell-Based Liquid Biopsy to Assess Protein Biomarkers and Cancer Genomics Using the RareCyte(®) Platform
title_full Beyond Circulating Tumor Cell Enumeration: Cell-Based Liquid Biopsy to Assess Protein Biomarkers and Cancer Genomics Using the RareCyte(®) Platform
title_fullStr Beyond Circulating Tumor Cell Enumeration: Cell-Based Liquid Biopsy to Assess Protein Biomarkers and Cancer Genomics Using the RareCyte(®) Platform
title_full_unstemmed Beyond Circulating Tumor Cell Enumeration: Cell-Based Liquid Biopsy to Assess Protein Biomarkers and Cancer Genomics Using the RareCyte(®) Platform
title_short Beyond Circulating Tumor Cell Enumeration: Cell-Based Liquid Biopsy to Assess Protein Biomarkers and Cancer Genomics Using the RareCyte(®) Platform
title_sort beyond circulating tumor cell enumeration: cell-based liquid biopsy to assess protein biomarkers and cancer genomics using the rarecyte(®) platform
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927801/
https://www.ncbi.nlm.nih.gov/pubmed/35308236
http://dx.doi.org/10.3389/fphar.2022.835727
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