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Novel molecular targets in hepatocellular carcinoma
Globally, hepatocellular carcinoma (HCC) is a leading cause of cancer and cancer-related deaths. The therapeutic efficacy of locoregional and systemic treatment in patients with advanced HCC remains low, which results in a poor prognosis. The development of sorafenib for the treatment of HCC has res...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443834/ https://www.ncbi.nlm.nih.gov/pubmed/32879846 http://dx.doi.org/10.5306/wjco.v11.i8.589 |
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author | Chow, Ariel Ka-Man Yau, Simon Wing-Lung Ng, Lui |
author_facet | Chow, Ariel Ka-Man Yau, Simon Wing-Lung Ng, Lui |
author_sort | Chow, Ariel Ka-Man |
collection | PubMed |
description | Globally, hepatocellular carcinoma (HCC) is a leading cause of cancer and cancer-related deaths. The therapeutic efficacy of locoregional and systemic treatment in patients with advanced HCC remains low, which results in a poor prognosis. The development of sorafenib for the treatment of HCC has resulted in a new era of molecular targeted therapy for this disease. However, the median overall survival was reported to be barely higher in the sorafenib treatment group than in the control group. Hence, in this review we describe the importance of developing more effective targeted therapies for the management of advanced HCC. Recent investigations of molecular signaling pathways in several cancers have provided some insights into developing molecular therapies that target critical members of these signaling pathways. Proteins involved in the Hedgehog and Notch signaling pathways, Polo-like kinase 1, arginine, histone deacetylases and Glypican-3 can be potential targets in the treatment of HCC. Monotherapy has limited therapeutic efficacy due to the development of inhibitory feedback mechanisms and induction of chemoresistance. Thus, emphasis is now on the development of personalized and combination molecular targeted therapies that can serve as ideal therapeutic strategies for improved management of HCC. |
format | Online Article Text |
id | pubmed-7443834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-74438342020-09-01 Novel molecular targets in hepatocellular carcinoma Chow, Ariel Ka-Man Yau, Simon Wing-Lung Ng, Lui World J Clin Oncol Review Globally, hepatocellular carcinoma (HCC) is a leading cause of cancer and cancer-related deaths. The therapeutic efficacy of locoregional and systemic treatment in patients with advanced HCC remains low, which results in a poor prognosis. The development of sorafenib for the treatment of HCC has resulted in a new era of molecular targeted therapy for this disease. However, the median overall survival was reported to be barely higher in the sorafenib treatment group than in the control group. Hence, in this review we describe the importance of developing more effective targeted therapies for the management of advanced HCC. Recent investigations of molecular signaling pathways in several cancers have provided some insights into developing molecular therapies that target critical members of these signaling pathways. Proteins involved in the Hedgehog and Notch signaling pathways, Polo-like kinase 1, arginine, histone deacetylases and Glypican-3 can be potential targets in the treatment of HCC. Monotherapy has limited therapeutic efficacy due to the development of inhibitory feedback mechanisms and induction of chemoresistance. Thus, emphasis is now on the development of personalized and combination molecular targeted therapies that can serve as ideal therapeutic strategies for improved management of HCC. Baishideng Publishing Group Inc 2020-08-24 2020-08-24 /pmc/articles/PMC7443834/ /pubmed/32879846 http://dx.doi.org/10.5306/wjco.v11.i8.589 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Review Chow, Ariel Ka-Man Yau, Simon Wing-Lung Ng, Lui Novel molecular targets in hepatocellular carcinoma |
title | Novel molecular targets in hepatocellular carcinoma |
title_full | Novel molecular targets in hepatocellular carcinoma |
title_fullStr | Novel molecular targets in hepatocellular carcinoma |
title_full_unstemmed | Novel molecular targets in hepatocellular carcinoma |
title_short | Novel molecular targets in hepatocellular carcinoma |
title_sort | novel molecular targets in hepatocellular carcinoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443834/ https://www.ncbi.nlm.nih.gov/pubmed/32879846 http://dx.doi.org/10.5306/wjco.v11.i8.589 |
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