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Tumor Tropism of DNA Viruses for Oncolytic Virotherapy
Oncolytic viruses (OVs) have emerged as one of the most promising cancer immunotherapy agents that selectively target and kill cancer cells while sparing normal cells. OVs are from diverse families of viruses and can possess either a DNA or an RNA genome. These viruses also have either a natural or...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675630/ https://www.ncbi.nlm.nih.gov/pubmed/38005938 http://dx.doi.org/10.3390/v15112262 |
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author | Enow, Junior A. Sheikh, Hummad I. Rahman, Masmudur M. |
author_facet | Enow, Junior A. Sheikh, Hummad I. Rahman, Masmudur M. |
author_sort | Enow, Junior A. |
collection | PubMed |
description | Oncolytic viruses (OVs) have emerged as one of the most promising cancer immunotherapy agents that selectively target and kill cancer cells while sparing normal cells. OVs are from diverse families of viruses and can possess either a DNA or an RNA genome. These viruses also have either a natural or engineered tropism for cancer cells. Oncolytic DNA viruses have the additional advantage of a stable genome and multiple-transgene insertion capability without compromising infection or replication. Herpes simplex virus 1 (HSV-1), a member of the oncolytic DNA viruses, has been approved for the treatment of cancers. This success with HSV-1 was achievable by introducing multiple genetic modifications within the virus to enhance cancer selectivity and reduce the toxicity to healthy cells. Here, we review the natural characteristics of and genetically engineered changes in selected DNA viruses that enhance the tumor tropism of these oncolytic viruses. |
format | Online Article Text |
id | pubmed-10675630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106756302023-11-16 Tumor Tropism of DNA Viruses for Oncolytic Virotherapy Enow, Junior A. Sheikh, Hummad I. Rahman, Masmudur M. Viruses Review Oncolytic viruses (OVs) have emerged as one of the most promising cancer immunotherapy agents that selectively target and kill cancer cells while sparing normal cells. OVs are from diverse families of viruses and can possess either a DNA or an RNA genome. These viruses also have either a natural or engineered tropism for cancer cells. Oncolytic DNA viruses have the additional advantage of a stable genome and multiple-transgene insertion capability without compromising infection or replication. Herpes simplex virus 1 (HSV-1), a member of the oncolytic DNA viruses, has been approved for the treatment of cancers. This success with HSV-1 was achievable by introducing multiple genetic modifications within the virus to enhance cancer selectivity and reduce the toxicity to healthy cells. Here, we review the natural characteristics of and genetically engineered changes in selected DNA viruses that enhance the tumor tropism of these oncolytic viruses. MDPI 2023-11-16 /pmc/articles/PMC10675630/ /pubmed/38005938 http://dx.doi.org/10.3390/v15112262 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 Enow, Junior A. Sheikh, Hummad I. Rahman, Masmudur M. Tumor Tropism of DNA Viruses for Oncolytic Virotherapy |
title | Tumor Tropism of DNA Viruses for Oncolytic Virotherapy |
title_full | Tumor Tropism of DNA Viruses for Oncolytic Virotherapy |
title_fullStr | Tumor Tropism of DNA Viruses for Oncolytic Virotherapy |
title_full_unstemmed | Tumor Tropism of DNA Viruses for Oncolytic Virotherapy |
title_short | Tumor Tropism of DNA Viruses for Oncolytic Virotherapy |
title_sort | tumor tropism of dna viruses for oncolytic virotherapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675630/ https://www.ncbi.nlm.nih.gov/pubmed/38005938 http://dx.doi.org/10.3390/v15112262 |
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