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Prospects for Comprehensive Analyses of Circulating Tumor Cells in Tumor Biology

The comprehensive analysis of biological and clinical aspects of circulating tumor cells (CTCs) has attracted interest as a means of enabling non-invasive, real-time monitoring of cancer patients and enhancing our fundamental understanding of tumor metastasis. However, CTC populations are extremely...

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Autores principales: Aoki, Masahiko, Shoji, Hirokazu, Kashiro, Ayumi, Takeuchi, Keiko, Shimizu, Yoshihiro, Honda, Kazufumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281475/
https://www.ncbi.nlm.nih.gov/pubmed/32369927
http://dx.doi.org/10.3390/cancers12051135
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author Aoki, Masahiko
Shoji, Hirokazu
Kashiro, Ayumi
Takeuchi, Keiko
Shimizu, Yoshihiro
Honda, Kazufumi
author_facet Aoki, Masahiko
Shoji, Hirokazu
Kashiro, Ayumi
Takeuchi, Keiko
Shimizu, Yoshihiro
Honda, Kazufumi
author_sort Aoki, Masahiko
collection PubMed
description The comprehensive analysis of biological and clinical aspects of circulating tumor cells (CTCs) has attracted interest as a means of enabling non-invasive, real-time monitoring of cancer patients and enhancing our fundamental understanding of tumor metastasis. However, CTC populations are extremely small when compared to other cell populations in the blood, limiting our comprehension of CTC biology and their clinical utility. Recently developed proteomic and genomic techniques that require only a small amount of sample have attracted much interest and expanded the potential utility of CTCs. Cancer heterogeneity, including specific mutations, greatly impacts disease diagnosis and the choice of available therapeutic strategies. The CTC population consists primarily of cancer stem cells, and CTC subpopulations are thought to undergo epithelial–mesenchymal transition during dissemination. To better characterize tumor cell populations, we demonstrated that changes in genomic profiles identified via next-generation sequencing of liquid biopsy samples could be expanded upon to increase sensitivity without decreasing specificity by using a combination of assays with CTCs and circulating tumor DNA. To enhance our understanding of CTC biology, we developed a metabolome analysis method applicable to single CTCs. Here, we review―omics studies related to CTC analysis and discuss various clinical and biological issues related to CTCs.
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spelling pubmed-72814752020-06-17 Prospects for Comprehensive Analyses of Circulating Tumor Cells in Tumor Biology Aoki, Masahiko Shoji, Hirokazu Kashiro, Ayumi Takeuchi, Keiko Shimizu, Yoshihiro Honda, Kazufumi Cancers (Basel) Review The comprehensive analysis of biological and clinical aspects of circulating tumor cells (CTCs) has attracted interest as a means of enabling non-invasive, real-time monitoring of cancer patients and enhancing our fundamental understanding of tumor metastasis. However, CTC populations are extremely small when compared to other cell populations in the blood, limiting our comprehension of CTC biology and their clinical utility. Recently developed proteomic and genomic techniques that require only a small amount of sample have attracted much interest and expanded the potential utility of CTCs. Cancer heterogeneity, including specific mutations, greatly impacts disease diagnosis and the choice of available therapeutic strategies. The CTC population consists primarily of cancer stem cells, and CTC subpopulations are thought to undergo epithelial–mesenchymal transition during dissemination. To better characterize tumor cell populations, we demonstrated that changes in genomic profiles identified via next-generation sequencing of liquid biopsy samples could be expanded upon to increase sensitivity without decreasing specificity by using a combination of assays with CTCs and circulating tumor DNA. To enhance our understanding of CTC biology, we developed a metabolome analysis method applicable to single CTCs. Here, we review―omics studies related to CTC analysis and discuss various clinical and biological issues related to CTCs. MDPI 2020-05-01 /pmc/articles/PMC7281475/ /pubmed/32369927 http://dx.doi.org/10.3390/cancers12051135 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Aoki, Masahiko
Shoji, Hirokazu
Kashiro, Ayumi
Takeuchi, Keiko
Shimizu, Yoshihiro
Honda, Kazufumi
Prospects for Comprehensive Analyses of Circulating Tumor Cells in Tumor Biology
title Prospects for Comprehensive Analyses of Circulating Tumor Cells in Tumor Biology
title_full Prospects for Comprehensive Analyses of Circulating Tumor Cells in Tumor Biology
title_fullStr Prospects for Comprehensive Analyses of Circulating Tumor Cells in Tumor Biology
title_full_unstemmed Prospects for Comprehensive Analyses of Circulating Tumor Cells in Tumor Biology
title_short Prospects for Comprehensive Analyses of Circulating Tumor Cells in Tumor Biology
title_sort prospects for comprehensive analyses of circulating tumor cells in tumor biology
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7281475/
https://www.ncbi.nlm.nih.gov/pubmed/32369927
http://dx.doi.org/10.3390/cancers12051135
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