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Detection of circulating tumor cells: opportunities and challenges
Circulating tumor cells (CTCs) are cells that shed from a primary tumor and travel through the bloodstream. Studying the functional and molecular characteristics of CTCs may provide in-depth knowledge regarding highly lethal tumor diseases. Researchers are working to design devices and develop analy...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9375360/ https://www.ncbi.nlm.nih.gov/pubmed/35962400 http://dx.doi.org/10.1186/s40364-022-00403-2 |
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author | Ju, Siwei Chen, Cong Zhang, Jiahang Xu, Lin Zhang, Xun Li, Zhaoqing Chen, Yongxia Zhou, Jichun Ji, Feiyang Wang, Linbo |
author_facet | Ju, Siwei Chen, Cong Zhang, Jiahang Xu, Lin Zhang, Xun Li, Zhaoqing Chen, Yongxia Zhou, Jichun Ji, Feiyang Wang, Linbo |
author_sort | Ju, Siwei |
collection | PubMed |
description | Circulating tumor cells (CTCs) are cells that shed from a primary tumor and travel through the bloodstream. Studying the functional and molecular characteristics of CTCs may provide in-depth knowledge regarding highly lethal tumor diseases. Researchers are working to design devices and develop analytical methods that can capture and detect CTCs in whole blood from cancer patients with improved sensitivity and specificity. Techniques using whole blood samples utilize physical prosperity, immunoaffinity or a combination of the above methods and positive and negative enrichment during separation. Further analysis of CTCs is helpful in cancer monitoring, efficacy evaluation and designing of targeted cancer treatment methods. Although many advances have been achieved in the detection and molecular characterization of CTCs, several challenges still exist that limit the current use of this burgeoning diagnostic approach. In this review, a brief summary of the biological characterization of CTCs is presented. We focus on the current existing CTC detection methods and the potential clinical implications and challenges of CTCs. We also put forward our own views regarding the future development direction of CTCs. |
format | Online Article Text |
id | pubmed-9375360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-93753602022-08-14 Detection of circulating tumor cells: opportunities and challenges Ju, Siwei Chen, Cong Zhang, Jiahang Xu, Lin Zhang, Xun Li, Zhaoqing Chen, Yongxia Zhou, Jichun Ji, Feiyang Wang, Linbo Biomark Res Review Circulating tumor cells (CTCs) are cells that shed from a primary tumor and travel through the bloodstream. Studying the functional and molecular characteristics of CTCs may provide in-depth knowledge regarding highly lethal tumor diseases. Researchers are working to design devices and develop analytical methods that can capture and detect CTCs in whole blood from cancer patients with improved sensitivity and specificity. Techniques using whole blood samples utilize physical prosperity, immunoaffinity or a combination of the above methods and positive and negative enrichment during separation. Further analysis of CTCs is helpful in cancer monitoring, efficacy evaluation and designing of targeted cancer treatment methods. Although many advances have been achieved in the detection and molecular characterization of CTCs, several challenges still exist that limit the current use of this burgeoning diagnostic approach. In this review, a brief summary of the biological characterization of CTCs is presented. We focus on the current existing CTC detection methods and the potential clinical implications and challenges of CTCs. We also put forward our own views regarding the future development direction of CTCs. BioMed Central 2022-08-13 /pmc/articles/PMC9375360/ /pubmed/35962400 http://dx.doi.org/10.1186/s40364-022-00403-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Ju, Siwei Chen, Cong Zhang, Jiahang Xu, Lin Zhang, Xun Li, Zhaoqing Chen, Yongxia Zhou, Jichun Ji, Feiyang Wang, Linbo Detection of circulating tumor cells: opportunities and challenges |
title | Detection of circulating tumor cells: opportunities and challenges |
title_full | Detection of circulating tumor cells: opportunities and challenges |
title_fullStr | Detection of circulating tumor cells: opportunities and challenges |
title_full_unstemmed | Detection of circulating tumor cells: opportunities and challenges |
title_short | Detection of circulating tumor cells: opportunities and challenges |
title_sort | detection of circulating tumor cells: opportunities and challenges |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9375360/ https://www.ncbi.nlm.nih.gov/pubmed/35962400 http://dx.doi.org/10.1186/s40364-022-00403-2 |
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