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Plasma Epstein–Barr virus DNA as an archetypal circulating tumour DNA marker
Analysis of circulating tumour DNA (ctDNA), as one type of ‘liquid biopsy’, has recently attracted great attention. Researchers are exploring many potential applications of liquid biopsy in many different types of cancer. In particular, it is of biological interest and clinical relevance to study th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594142/ https://www.ncbi.nlm.nih.gov/pubmed/30714167 http://dx.doi.org/10.1002/path.5249 |
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author | Lam, Wai Kei Jacky Chan, Kwan Chee Allen Lo, Yuk Ming Dennis |
author_facet | Lam, Wai Kei Jacky Chan, Kwan Chee Allen Lo, Yuk Ming Dennis |
author_sort | Lam, Wai Kei Jacky |
collection | PubMed |
description | Analysis of circulating tumour DNA (ctDNA), as one type of ‘liquid biopsy’, has recently attracted great attention. Researchers are exploring many potential applications of liquid biopsy in many different types of cancer. In particular, it is of biological interest and clinical relevance to study the molecular characteristics of ctDNA. For such purposes, plasma Epstein–Barr virus (EBV) DNA from patients with nasopharyngeal carcinoma (NPC) would provide a good model to understand the biological properties and clinical applications of ctDNA in general. The strong association between EBV and NPC in endemic regions has made plasma EBV DNA a robust biomarker for this cancer. There are many clinical utilities of plasma EBV DNA analysis in NPC diagnostics. Its role in prognostication and surveillance of recurrence is well established. Plasma EBV DNA has also been validated for screening NPC in a recent large‐scale prospective study. Indeed, plasma EBV DNA could be regarded as an archetypal ctDNA marker. In this review, we discuss the biological properties of plasma EBV DNA from NPC samples and also the clinical applications of plasma EBV DNA analysis in the management of NPC. Of note, the recently reported size analysis of plasma EBV DNA in patients with NPC has highlighted size as an important analytical parameter of ctDNA and demonstrated clinical value in improving the diagnostic performance of an EBV DNA‐based NPC screening test. Such insights into ctDNA analysis (including size profiling) may help its full potential in cancer diagnostics for other types of cancer to be realised. © 2019 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland. |
format | Online Article Text |
id | pubmed-6594142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-65941422019-07-10 Plasma Epstein–Barr virus DNA as an archetypal circulating tumour DNA marker Lam, Wai Kei Jacky Chan, Kwan Chee Allen Lo, Yuk Ming Dennis J Pathol Invited Reviews Analysis of circulating tumour DNA (ctDNA), as one type of ‘liquid biopsy’, has recently attracted great attention. Researchers are exploring many potential applications of liquid biopsy in many different types of cancer. In particular, it is of biological interest and clinical relevance to study the molecular characteristics of ctDNA. For such purposes, plasma Epstein–Barr virus (EBV) DNA from patients with nasopharyngeal carcinoma (NPC) would provide a good model to understand the biological properties and clinical applications of ctDNA in general. The strong association between EBV and NPC in endemic regions has made plasma EBV DNA a robust biomarker for this cancer. There are many clinical utilities of plasma EBV DNA analysis in NPC diagnostics. Its role in prognostication and surveillance of recurrence is well established. Plasma EBV DNA has also been validated for screening NPC in a recent large‐scale prospective study. Indeed, plasma EBV DNA could be regarded as an archetypal ctDNA marker. In this review, we discuss the biological properties of plasma EBV DNA from NPC samples and also the clinical applications of plasma EBV DNA analysis in the management of NPC. Of note, the recently reported size analysis of plasma EBV DNA in patients with NPC has highlighted size as an important analytical parameter of ctDNA and demonstrated clinical value in improving the diagnostic performance of an EBV DNA‐based NPC screening test. Such insights into ctDNA analysis (including size profiling) may help its full potential in cancer diagnostics for other types of cancer to be realised. © 2019 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland. John Wiley & Sons, Ltd 2019-02-25 2019-04 /pmc/articles/PMC6594142/ /pubmed/30714167 http://dx.doi.org/10.1002/path.5249 Text en © 2019 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Invited Reviews Lam, Wai Kei Jacky Chan, Kwan Chee Allen Lo, Yuk Ming Dennis Plasma Epstein–Barr virus DNA as an archetypal circulating tumour DNA marker |
title | Plasma Epstein–Barr virus DNA as an archetypal circulating tumour DNA marker |
title_full | Plasma Epstein–Barr virus DNA as an archetypal circulating tumour DNA marker |
title_fullStr | Plasma Epstein–Barr virus DNA as an archetypal circulating tumour DNA marker |
title_full_unstemmed | Plasma Epstein–Barr virus DNA as an archetypal circulating tumour DNA marker |
title_short | Plasma Epstein–Barr virus DNA as an archetypal circulating tumour DNA marker |
title_sort | plasma epstein–barr virus dna as an archetypal circulating tumour dna marker |
topic | Invited Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6594142/ https://www.ncbi.nlm.nih.gov/pubmed/30714167 http://dx.doi.org/10.1002/path.5249 |
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