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Genetics of Hepatocellular Carcinoma: From Tumor to Circulating DNA

SIMPLE SUMMARY: In recent years, the genetic landscape of hepatocellular carcinoma (HCC) has been explored, identifying TERT promoter, CTNNB1, and TP53 as the most frequent mutated genes. Therapies directed against specific targetable genomic alterations are the basis of personalized medicine and re...

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Autores principales: Campani, Claudia, Zucman-Rossi, Jessica, Nault, Jean-Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9913369/
https://www.ncbi.nlm.nih.gov/pubmed/36765775
http://dx.doi.org/10.3390/cancers15030817
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author Campani, Claudia
Zucman-Rossi, Jessica
Nault, Jean-Charles
author_facet Campani, Claudia
Zucman-Rossi, Jessica
Nault, Jean-Charles
author_sort Campani, Claudia
collection PubMed
description SIMPLE SUMMARY: In recent years, the genetic landscape of hepatocellular carcinoma (HCC) has been explored, identifying TERT promoter, CTNNB1, and TP53 as the most frequent mutated genes. Therapies directed against specific targetable genomic alterations are the basis of personalized medicine and represent the cornerstone of systemic treatment for many malignancies, but are not yet available in HCC. Tools such as liquid biopsy and, in particular, circulating tumor DNA (ctDNA) may help in identifying biomarkers of response or resistance to treatment, and their role in HCC is an active field of research. In this review, we summarize the available evidence on the HCC genomic landscape and the potential role of ctDNA in clinical practice. ABSTRACT: Hepatocellular carcinoma (HCC) accounts for 90% of primary hepatic malignancies and is one of the major causes of cancer-related death. Over the last 15 years, the molecular landscape of HCC has been deciphered, with the identification of the main driver genes of liver carcinogenesis that belong to six major biological pathways, such as telomere maintenance, Wnt/b-catenin, P53/cell cycle regulation, oxidative stress, epigenetic modifiers, AKT/mTOR and MAP kinase. The combination of genetic and transcriptomic data composed various HCC subclasses strongly related to risk factors, pathological features and prognosis. However, translation into clinical practice is not achieved, mainly because the most frequently mutated genes are undruggable. Moreover, the results derived from the analysis of a single tissue sample may not adequately catch the intra- and intertumor heterogeneity. The analysis of circulating tumor DNA (ctDNA) is broadly developed in other types of cancer for early diagnosis, prognosis and monitoring under systemic treatment in order to identify primary and secondary mechanisms of resistance. The aim of this review is to describe recent data about the HCC molecular landscape and to discuss how ctDNA could be used in the future for HCC detection and management.
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spelling pubmed-99133692023-02-11 Genetics of Hepatocellular Carcinoma: From Tumor to Circulating DNA Campani, Claudia Zucman-Rossi, Jessica Nault, Jean-Charles Cancers (Basel) Review SIMPLE SUMMARY: In recent years, the genetic landscape of hepatocellular carcinoma (HCC) has been explored, identifying TERT promoter, CTNNB1, and TP53 as the most frequent mutated genes. Therapies directed against specific targetable genomic alterations are the basis of personalized medicine and represent the cornerstone of systemic treatment for many malignancies, but are not yet available in HCC. Tools such as liquid biopsy and, in particular, circulating tumor DNA (ctDNA) may help in identifying biomarkers of response or resistance to treatment, and their role in HCC is an active field of research. In this review, we summarize the available evidence on the HCC genomic landscape and the potential role of ctDNA in clinical practice. ABSTRACT: Hepatocellular carcinoma (HCC) accounts for 90% of primary hepatic malignancies and is one of the major causes of cancer-related death. Over the last 15 years, the molecular landscape of HCC has been deciphered, with the identification of the main driver genes of liver carcinogenesis that belong to six major biological pathways, such as telomere maintenance, Wnt/b-catenin, P53/cell cycle regulation, oxidative stress, epigenetic modifiers, AKT/mTOR and MAP kinase. The combination of genetic and transcriptomic data composed various HCC subclasses strongly related to risk factors, pathological features and prognosis. However, translation into clinical practice is not achieved, mainly because the most frequently mutated genes are undruggable. Moreover, the results derived from the analysis of a single tissue sample may not adequately catch the intra- and intertumor heterogeneity. The analysis of circulating tumor DNA (ctDNA) is broadly developed in other types of cancer for early diagnosis, prognosis and monitoring under systemic treatment in order to identify primary and secondary mechanisms of resistance. The aim of this review is to describe recent data about the HCC molecular landscape and to discuss how ctDNA could be used in the future for HCC detection and management. MDPI 2023-01-28 /pmc/articles/PMC9913369/ /pubmed/36765775 http://dx.doi.org/10.3390/cancers15030817 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Campani, Claudia
Zucman-Rossi, Jessica
Nault, Jean-Charles
Genetics of Hepatocellular Carcinoma: From Tumor to Circulating DNA
title Genetics of Hepatocellular Carcinoma: From Tumor to Circulating DNA
title_full Genetics of Hepatocellular Carcinoma: From Tumor to Circulating DNA
title_fullStr Genetics of Hepatocellular Carcinoma: From Tumor to Circulating DNA
title_full_unstemmed Genetics of Hepatocellular Carcinoma: From Tumor to Circulating DNA
title_short Genetics of Hepatocellular Carcinoma: From Tumor to Circulating DNA
title_sort genetics of hepatocellular carcinoma: from tumor to circulating dna
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9913369/
https://www.ncbi.nlm.nih.gov/pubmed/36765775
http://dx.doi.org/10.3390/cancers15030817
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