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Liquid biopsy and PCR-free ultrasensitive detection systems in oncology (Review)

In oncology, liquid biopsy is used in the detection of next-generation analytes, such as tumor cells, cell-free nucleic acids and exosomes in peripheral blood and other body fluids from cancer patients. It is considered one of the most advanced non-invasive diagnostic systems to enable clinically re...

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Autores principales: Finotti, Alessia, Allegretti, Matteo, Gasparello, Jessica, Giacomini, Patrizio, Spandidos, Demetrios A., Spoto, Giuseppe, Gambari, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086621/
https://www.ncbi.nlm.nih.gov/pubmed/30085333
http://dx.doi.org/10.3892/ijo.2018.4516
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author Finotti, Alessia
Allegretti, Matteo
Gasparello, Jessica
Giacomini, Patrizio
Spandidos, Demetrios A.
Spoto, Giuseppe
Gambari, Roberto
author_facet Finotti, Alessia
Allegretti, Matteo
Gasparello, Jessica
Giacomini, Patrizio
Spandidos, Demetrios A.
Spoto, Giuseppe
Gambari, Roberto
author_sort Finotti, Alessia
collection PubMed
description In oncology, liquid biopsy is used in the detection of next-generation analytes, such as tumor cells, cell-free nucleic acids and exosomes in peripheral blood and other body fluids from cancer patients. It is considered one of the most advanced non-invasive diagnostic systems to enable clinically relevant actions and implement precision medicine. Medical actions include, but are not limited to, early diagnosis, staging, prognosis, anticipation (lead time) and the prediction of therapy responses, as well as follow-up. Historically, the applications of liquid biopsy in cancer have focused on circulating tumor cells (CTCs). More recently, this analysis has been extended to circulating free DNA (cfDNA) and microRNAs (miRNAs or miRs) associated with cancer, with potential applications for development into multi-marker diagnostic, prognostic and therapeutic signatures. Liquid biopsies avoid some key limitations of conventional tumor tissue biopsies, including invasive tumor sampling, under-representation of tumor heterogeneity and poor description of clonal evolution during metastatic dissemination, strongly reducing the need for multiple sampling. On the other hand, this approach suffers from important drawbacks, i.e., the fragmentation of cfDNA, the instability of RNA, the low concentrations of certain analytes in body fluids and the confounding presence of normal, as well as aberrant DNAs and RNAs. For these reasons, the analysis of cfDNA has been mostly focused on mutations arising in, and pathognomonicity of, tumor DNA, while the analysis of cfRNA has been mostly focused on miRNA patterns strongly associated with neoplastic transformation/progression. This review lists some major applicative areas, briefly addresses how technology is bypassing liquid biopsy limitations, and places a particular emphasis on novel, PCR-free platforms. The ongoing collaborative efforts of major international consortia are reviewed. In addition to basic and applied research, we will consider technological transfer, including patents, patent applications and available information on clinical trials aimed at verifying the potential of liquid biopsy in cancer.
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spelling pubmed-60866212018-08-13 Liquid biopsy and PCR-free ultrasensitive detection systems in oncology (Review) Finotti, Alessia Allegretti, Matteo Gasparello, Jessica Giacomini, Patrizio Spandidos, Demetrios A. Spoto, Giuseppe Gambari, Roberto Int J Oncol Articles In oncology, liquid biopsy is used in the detection of next-generation analytes, such as tumor cells, cell-free nucleic acids and exosomes in peripheral blood and other body fluids from cancer patients. It is considered one of the most advanced non-invasive diagnostic systems to enable clinically relevant actions and implement precision medicine. Medical actions include, but are not limited to, early diagnosis, staging, prognosis, anticipation (lead time) and the prediction of therapy responses, as well as follow-up. Historically, the applications of liquid biopsy in cancer have focused on circulating tumor cells (CTCs). More recently, this analysis has been extended to circulating free DNA (cfDNA) and microRNAs (miRNAs or miRs) associated with cancer, with potential applications for development into multi-marker diagnostic, prognostic and therapeutic signatures. Liquid biopsies avoid some key limitations of conventional tumor tissue biopsies, including invasive tumor sampling, under-representation of tumor heterogeneity and poor description of clonal evolution during metastatic dissemination, strongly reducing the need for multiple sampling. On the other hand, this approach suffers from important drawbacks, i.e., the fragmentation of cfDNA, the instability of RNA, the low concentrations of certain analytes in body fluids and the confounding presence of normal, as well as aberrant DNAs and RNAs. For these reasons, the analysis of cfDNA has been mostly focused on mutations arising in, and pathognomonicity of, tumor DNA, while the analysis of cfRNA has been mostly focused on miRNA patterns strongly associated with neoplastic transformation/progression. This review lists some major applicative areas, briefly addresses how technology is bypassing liquid biopsy limitations, and places a particular emphasis on novel, PCR-free platforms. The ongoing collaborative efforts of major international consortia are reviewed. In addition to basic and applied research, we will consider technological transfer, including patents, patent applications and available information on clinical trials aimed at verifying the potential of liquid biopsy in cancer. D.A. Spandidos 2018-08-06 /pmc/articles/PMC6086621/ /pubmed/30085333 http://dx.doi.org/10.3892/ijo.2018.4516 Text en Copyright: © Finotti et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Finotti, Alessia
Allegretti, Matteo
Gasparello, Jessica
Giacomini, Patrizio
Spandidos, Demetrios A.
Spoto, Giuseppe
Gambari, Roberto
Liquid biopsy and PCR-free ultrasensitive detection systems in oncology (Review)
title Liquid biopsy and PCR-free ultrasensitive detection systems in oncology (Review)
title_full Liquid biopsy and PCR-free ultrasensitive detection systems in oncology (Review)
title_fullStr Liquid biopsy and PCR-free ultrasensitive detection systems in oncology (Review)
title_full_unstemmed Liquid biopsy and PCR-free ultrasensitive detection systems in oncology (Review)
title_short Liquid biopsy and PCR-free ultrasensitive detection systems in oncology (Review)
title_sort liquid biopsy and pcr-free ultrasensitive detection systems in oncology (review)
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086621/
https://www.ncbi.nlm.nih.gov/pubmed/30085333
http://dx.doi.org/10.3892/ijo.2018.4516
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