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HCC biomarkers – state of the old and outlook to future promising biomarkers and their potential in everyday clinical practice
Hepatocellular carcinoma (HCC) is one of the most common and deadly tumors worldwide. Management of HCC depends on reliable biomarkers for screening, diagnosis, and monitoring of the disease, as well as predicting response towards therapy and safety. To date, imaging has been the established standar...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742592/ https://www.ncbi.nlm.nih.gov/pubmed/36518320 http://dx.doi.org/10.3389/fonc.2022.1016952 |
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author | Schlosser, Sophie Tümen, Deniz Volz, Barbara Neumeyer, Katja Egler, Niklas Kunst, Claudia Tews, Hauke Christian Schmid, Stephan Kandulski, Arne Müller, Martina Gülow, Karsten |
author_facet | Schlosser, Sophie Tümen, Deniz Volz, Barbara Neumeyer, Katja Egler, Niklas Kunst, Claudia Tews, Hauke Christian Schmid, Stephan Kandulski, Arne Müller, Martina Gülow, Karsten |
author_sort | Schlosser, Sophie |
collection | PubMed |
description | Hepatocellular carcinoma (HCC) is one of the most common and deadly tumors worldwide. Management of HCC depends on reliable biomarkers for screening, diagnosis, and monitoring of the disease, as well as predicting response towards therapy and safety. To date, imaging has been the established standard technique in the diagnosis and follow-up of HCC. However, imaging techniques have their limitations, especially in the early detection of HCC. Therefore, there is an urgent need for reliable, non/minimal invasive biomarkers. To date, alpha-fetoprotein (AFP) is the only serum biomarker used in clinical practice for the management of HCC. However, AFP is of relatively rather low quality in terms of specificity and sensitivity. Liquid biopsies as a source for biomarkers have become the focus of clinical research. Our review highlights alternative biomarkers derived from liquid biopsies, including circulating tumor cells, proteins, circulating nucleic acids, and exosomes, and their potential for clinical application. Using defined combinations of different biomarkers will open new perspectives for diagnosing, treating, and monitoring HCC. |
format | Online Article Text |
id | pubmed-9742592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97425922022-12-13 HCC biomarkers – state of the old and outlook to future promising biomarkers and their potential in everyday clinical practice Schlosser, Sophie Tümen, Deniz Volz, Barbara Neumeyer, Katja Egler, Niklas Kunst, Claudia Tews, Hauke Christian Schmid, Stephan Kandulski, Arne Müller, Martina Gülow, Karsten Front Oncol Oncology Hepatocellular carcinoma (HCC) is one of the most common and deadly tumors worldwide. Management of HCC depends on reliable biomarkers for screening, diagnosis, and monitoring of the disease, as well as predicting response towards therapy and safety. To date, imaging has been the established standard technique in the diagnosis and follow-up of HCC. However, imaging techniques have their limitations, especially in the early detection of HCC. Therefore, there is an urgent need for reliable, non/minimal invasive biomarkers. To date, alpha-fetoprotein (AFP) is the only serum biomarker used in clinical practice for the management of HCC. However, AFP is of relatively rather low quality in terms of specificity and sensitivity. Liquid biopsies as a source for biomarkers have become the focus of clinical research. Our review highlights alternative biomarkers derived from liquid biopsies, including circulating tumor cells, proteins, circulating nucleic acids, and exosomes, and their potential for clinical application. Using defined combinations of different biomarkers will open new perspectives for diagnosing, treating, and monitoring HCC. Frontiers Media S.A. 2022-11-28 /pmc/articles/PMC9742592/ /pubmed/36518320 http://dx.doi.org/10.3389/fonc.2022.1016952 Text en Copyright © 2022 Schlosser, Tümen, Volz, Neumeyer, Egler, Kunst, Tews, Schmid, Kandulski, Müller and Gülow 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 | Oncology Schlosser, Sophie Tümen, Deniz Volz, Barbara Neumeyer, Katja Egler, Niklas Kunst, Claudia Tews, Hauke Christian Schmid, Stephan Kandulski, Arne Müller, Martina Gülow, Karsten HCC biomarkers – state of the old and outlook to future promising biomarkers and their potential in everyday clinical practice |
title | HCC biomarkers – state of the old and outlook to future promising biomarkers and their potential in everyday clinical practice |
title_full | HCC biomarkers – state of the old and outlook to future promising biomarkers and their potential in everyday clinical practice |
title_fullStr | HCC biomarkers – state of the old and outlook to future promising biomarkers and their potential in everyday clinical practice |
title_full_unstemmed | HCC biomarkers – state of the old and outlook to future promising biomarkers and their potential in everyday clinical practice |
title_short | HCC biomarkers – state of the old and outlook to future promising biomarkers and their potential in everyday clinical practice |
title_sort | hcc biomarkers – state of the old and outlook to future promising biomarkers and their potential in everyday clinical practice |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742592/ https://www.ncbi.nlm.nih.gov/pubmed/36518320 http://dx.doi.org/10.3389/fonc.2022.1016952 |
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