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Oncolytic virotherapy in hepato‐bilio‐pancreatic cancer: The key to breaking the log jam?

Traditional therapies have limited efficacy in hepatocellular carcinoma, pancreatic cancer, and biliary tract cancer, especially for advanced and refractory cancers. Through a deeper understanding of antitumor immunity and the tumor microenvironment, novel immunotherapies are becoming available for...

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Detalles Bibliográficos
Autores principales: Li, Yuwei, Shen, Yinan, Zhao, Ronghua, Samudio, Ismael, Jia, William, Bai, Xueli, Liang, Tingbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196045/
https://www.ncbi.nlm.nih.gov/pubmed/32130786
http://dx.doi.org/10.1002/cam4.2949
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author Li, Yuwei
Shen, Yinan
Zhao, Ronghua
Samudio, Ismael
Jia, William
Bai, Xueli
Liang, Tingbo
author_facet Li, Yuwei
Shen, Yinan
Zhao, Ronghua
Samudio, Ismael
Jia, William
Bai, Xueli
Liang, Tingbo
author_sort Li, Yuwei
collection PubMed
description Traditional therapies have limited efficacy in hepatocellular carcinoma, pancreatic cancer, and biliary tract cancer, especially for advanced and refractory cancers. Through a deeper understanding of antitumor immunity and the tumor microenvironment, novel immunotherapies are becoming available for cancer treatment. Oncolytic virus (OV) therapy is an emerging type of immunotherapy that has demonstrated effective antitumor efficacy in many preclinical studies and clinical studies. Thus, it may represent a potential feasible treatment for hard to treat gastrointestinal (GI) tumors. Here, we summarize the research progress of OV therapy for the treatment of hepato‐bilio‐pancreatic cancers. In general, most OV therapies exhibits potent, specific oncolysis both in cell lines in vitro and the animal models in vivo. Currently, several clinical trials have suggested that OV therapy may also be effective in patients with refractory hepato‐bilio‐pancreatic cancer. Multiple strategies such as introducing immunostimulatory genes, modifying virus capsid and combining various other therapeutic modalities have been shown enhanced specific oncolysis and synergistic anti‐cancer immune stimulation. Combining OV with other antitumor therapies may become a more effective strategy than using virus alone. Nevertheless, more studies are needed to better understand the mechanisms underlying the therapeutic effects of OV, and to design appropriate dosing and combination strategies.
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spelling pubmed-71960452020-05-04 Oncolytic virotherapy in hepato‐bilio‐pancreatic cancer: The key to breaking the log jam? Li, Yuwei Shen, Yinan Zhao, Ronghua Samudio, Ismael Jia, William Bai, Xueli Liang, Tingbo Cancer Med Clinical Cancer Research Traditional therapies have limited efficacy in hepatocellular carcinoma, pancreatic cancer, and biliary tract cancer, especially for advanced and refractory cancers. Through a deeper understanding of antitumor immunity and the tumor microenvironment, novel immunotherapies are becoming available for cancer treatment. Oncolytic virus (OV) therapy is an emerging type of immunotherapy that has demonstrated effective antitumor efficacy in many preclinical studies and clinical studies. Thus, it may represent a potential feasible treatment for hard to treat gastrointestinal (GI) tumors. Here, we summarize the research progress of OV therapy for the treatment of hepato‐bilio‐pancreatic cancers. In general, most OV therapies exhibits potent, specific oncolysis both in cell lines in vitro and the animal models in vivo. Currently, several clinical trials have suggested that OV therapy may also be effective in patients with refractory hepato‐bilio‐pancreatic cancer. Multiple strategies such as introducing immunostimulatory genes, modifying virus capsid and combining various other therapeutic modalities have been shown enhanced specific oncolysis and synergistic anti‐cancer immune stimulation. Combining OV with other antitumor therapies may become a more effective strategy than using virus alone. Nevertheless, more studies are needed to better understand the mechanisms underlying the therapeutic effects of OV, and to design appropriate dosing and combination strategies. John Wiley and Sons Inc. 2020-03-04 /pmc/articles/PMC7196045/ /pubmed/32130786 http://dx.doi.org/10.1002/cam4.2949 Text en © 2020 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. 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 Clinical Cancer Research
Li, Yuwei
Shen, Yinan
Zhao, Ronghua
Samudio, Ismael
Jia, William
Bai, Xueli
Liang, Tingbo
Oncolytic virotherapy in hepato‐bilio‐pancreatic cancer: The key to breaking the log jam?
title Oncolytic virotherapy in hepato‐bilio‐pancreatic cancer: The key to breaking the log jam?
title_full Oncolytic virotherapy in hepato‐bilio‐pancreatic cancer: The key to breaking the log jam?
title_fullStr Oncolytic virotherapy in hepato‐bilio‐pancreatic cancer: The key to breaking the log jam?
title_full_unstemmed Oncolytic virotherapy in hepato‐bilio‐pancreatic cancer: The key to breaking the log jam?
title_short Oncolytic virotherapy in hepato‐bilio‐pancreatic cancer: The key to breaking the log jam?
title_sort oncolytic virotherapy in hepato‐bilio‐pancreatic cancer: the key to breaking the log jam?
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196045/
https://www.ncbi.nlm.nih.gov/pubmed/32130786
http://dx.doi.org/10.1002/cam4.2949
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