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The Immune System in Hepatocellular Carcinoma and Potential New Immunotherapeutic Strategies
BACKGROUND: Hepatocellular carcinoma is a major health problem worldwide and the third most common cause of cancer-related death. HCC treatment decisions are complex and dependent upon tumor staging. Several molecular targeted agents have been evaluated in clinical trials in advanced HCC. Despite of...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393929/ https://www.ncbi.nlm.nih.gov/pubmed/25893197 http://dx.doi.org/10.1155/2015/731469 |
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author | Bertino, Gaetano Demma, Shirin Ardiri, Annalisa Proiti, Maria Malaguarnera, Giulia Bertino, Nicoletta Malaguarnera, Mariano Malaguarnera, Michele |
author_facet | Bertino, Gaetano Demma, Shirin Ardiri, Annalisa Proiti, Maria Malaguarnera, Giulia Bertino, Nicoletta Malaguarnera, Mariano Malaguarnera, Michele |
author_sort | Bertino, Gaetano |
collection | PubMed |
description | BACKGROUND: Hepatocellular carcinoma is a major health problem worldwide and the third most common cause of cancer-related death. HCC treatment decisions are complex and dependent upon tumor staging. Several molecular targeted agents have been evaluated in clinical trials in advanced HCC. Despite of only modest objective response rates according to the Response Evaluation Criteria in Solid Tumors, several studies showed encouraging results in terms of prolongation of the time to progression, disease stabilization, and survival. Cellular immunotherapy would improve the immune state and has potential in enhancing the therapeutic outcome for HCC patients. MATERIALS AND METHODS: A search of the literature was made using cancer literature, the PubMed, Scopus, and Web of Science (WOS) database for the following keywords: “hepatocellular carcinoma,” “molecular hepatocarcinogenesis,” “targeted therapy,” “molecular immunological targets,” “tumour-associated antigens,” “Tregs,” “MDSCs,” “immunotherapy.” Discussion and Conclusion. Treatment strategies combining blockade of immunoregulatory cell types such as Tregs and MDSCs and of inhibitory receptors, with vaccine-induced activation of TAA-specific T cells, may be necessary to achieve the most effective therapeutic antitumour activity in HCC. In the future, new therapeutic options will be represented by a blend of immunotherapy-like vaccines and T-cell modulators, supplemented by molecularly targeted inhibitors of tumor signaling pathways. |
format | Online Article Text |
id | pubmed-4393929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-43939292015-04-19 The Immune System in Hepatocellular Carcinoma and Potential New Immunotherapeutic Strategies Bertino, Gaetano Demma, Shirin Ardiri, Annalisa Proiti, Maria Malaguarnera, Giulia Bertino, Nicoletta Malaguarnera, Mariano Malaguarnera, Michele Biomed Res Int Review Article BACKGROUND: Hepatocellular carcinoma is a major health problem worldwide and the third most common cause of cancer-related death. HCC treatment decisions are complex and dependent upon tumor staging. Several molecular targeted agents have been evaluated in clinical trials in advanced HCC. Despite of only modest objective response rates according to the Response Evaluation Criteria in Solid Tumors, several studies showed encouraging results in terms of prolongation of the time to progression, disease stabilization, and survival. Cellular immunotherapy would improve the immune state and has potential in enhancing the therapeutic outcome for HCC patients. MATERIALS AND METHODS: A search of the literature was made using cancer literature, the PubMed, Scopus, and Web of Science (WOS) database for the following keywords: “hepatocellular carcinoma,” “molecular hepatocarcinogenesis,” “targeted therapy,” “molecular immunological targets,” “tumour-associated antigens,” “Tregs,” “MDSCs,” “immunotherapy.” Discussion and Conclusion. Treatment strategies combining blockade of immunoregulatory cell types such as Tregs and MDSCs and of inhibitory receptors, with vaccine-induced activation of TAA-specific T cells, may be necessary to achieve the most effective therapeutic antitumour activity in HCC. In the future, new therapeutic options will be represented by a blend of immunotherapy-like vaccines and T-cell modulators, supplemented by molecularly targeted inhibitors of tumor signaling pathways. Hindawi Publishing Corporation 2015 2015-03-29 /pmc/articles/PMC4393929/ /pubmed/25893197 http://dx.doi.org/10.1155/2015/731469 Text en Copyright © 2015 Gaetano Bertino et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Bertino, Gaetano Demma, Shirin Ardiri, Annalisa Proiti, Maria Malaguarnera, Giulia Bertino, Nicoletta Malaguarnera, Mariano Malaguarnera, Michele The Immune System in Hepatocellular Carcinoma and Potential New Immunotherapeutic Strategies |
title | The Immune System in Hepatocellular Carcinoma and Potential New Immunotherapeutic Strategies |
title_full | The Immune System in Hepatocellular Carcinoma and Potential New Immunotherapeutic Strategies |
title_fullStr | The Immune System in Hepatocellular Carcinoma and Potential New Immunotherapeutic Strategies |
title_full_unstemmed | The Immune System in Hepatocellular Carcinoma and Potential New Immunotherapeutic Strategies |
title_short | The Immune System in Hepatocellular Carcinoma and Potential New Immunotherapeutic Strategies |
title_sort | immune system in hepatocellular carcinoma and potential new immunotherapeutic strategies |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393929/ https://www.ncbi.nlm.nih.gov/pubmed/25893197 http://dx.doi.org/10.1155/2015/731469 |
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