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The Evolution and Future of Targeted Cancer Therapy: From Nanoparticles, Oncolytic Viruses, and Oncolytic Bacteria to the Treatment of Solid Tumors

While many classes of chemotherapeutic agents exist to treat solid tumors, few can generate a lasting response without substantial off-target toxicity despite significant scientific advancements and investments. In this review, the paths of development for nanoparticles, oncolytic viruses, and oncol...

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Autores principales: Pierce, Kyle M., Miklavcic, William R., Cook, Kyle P., Hennen, Mikayla Sweitzer, Bayles, Kenneth W., Hollingsworth, Michael A., Brooks, Amanda E., Pullan, Jessica E., Dailey, Kaitlin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623458/
https://www.ncbi.nlm.nih.gov/pubmed/34835785
http://dx.doi.org/10.3390/nano11113018
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author Pierce, Kyle M.
Miklavcic, William R.
Cook, Kyle P.
Hennen, Mikayla Sweitzer
Bayles, Kenneth W.
Hollingsworth, Michael A.
Brooks, Amanda E.
Pullan, Jessica E.
Dailey, Kaitlin M.
author_facet Pierce, Kyle M.
Miklavcic, William R.
Cook, Kyle P.
Hennen, Mikayla Sweitzer
Bayles, Kenneth W.
Hollingsworth, Michael A.
Brooks, Amanda E.
Pullan, Jessica E.
Dailey, Kaitlin M.
author_sort Pierce, Kyle M.
collection PubMed
description While many classes of chemotherapeutic agents exist to treat solid tumors, few can generate a lasting response without substantial off-target toxicity despite significant scientific advancements and investments. In this review, the paths of development for nanoparticles, oncolytic viruses, and oncolytic bacteria over the last 20 years of research towards clinical translation and acceptance as novel cancer therapeutics are compared. Novel nanoparticle, oncolytic virus, and oncolytic bacteria therapies all start with a common goal of accomplishing therapeutic drug activity or delivery to a specific site while avoiding off-target effects, with overlapping methodology between all three modalities. Indeed, the degree of overlap is substantial enough that breakthroughs in one therapeutic could have considerable implications on the progression of the other two. Each oncotherapeutic modality has accomplished clinical translation, successfully overcoming the potential pitfalls promising therapeutics face. However, once studies enter clinical trials, the data all but disappears, leaving pre-clinical researchers largely in the dark. Overall, the creativity, flexibility, and innovation of these modalities for solid tumor treatments are greatly encouraging, and usher in a new age of pharmaceutical development.
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spelling pubmed-86234582021-11-27 The Evolution and Future of Targeted Cancer Therapy: From Nanoparticles, Oncolytic Viruses, and Oncolytic Bacteria to the Treatment of Solid Tumors Pierce, Kyle M. Miklavcic, William R. Cook, Kyle P. Hennen, Mikayla Sweitzer Bayles, Kenneth W. Hollingsworth, Michael A. Brooks, Amanda E. Pullan, Jessica E. Dailey, Kaitlin M. Nanomaterials (Basel) Review While many classes of chemotherapeutic agents exist to treat solid tumors, few can generate a lasting response without substantial off-target toxicity despite significant scientific advancements and investments. In this review, the paths of development for nanoparticles, oncolytic viruses, and oncolytic bacteria over the last 20 years of research towards clinical translation and acceptance as novel cancer therapeutics are compared. Novel nanoparticle, oncolytic virus, and oncolytic bacteria therapies all start with a common goal of accomplishing therapeutic drug activity or delivery to a specific site while avoiding off-target effects, with overlapping methodology between all three modalities. Indeed, the degree of overlap is substantial enough that breakthroughs in one therapeutic could have considerable implications on the progression of the other two. Each oncotherapeutic modality has accomplished clinical translation, successfully overcoming the potential pitfalls promising therapeutics face. However, once studies enter clinical trials, the data all but disappears, leaving pre-clinical researchers largely in the dark. Overall, the creativity, flexibility, and innovation of these modalities for solid tumor treatments are greatly encouraging, and usher in a new age of pharmaceutical development. MDPI 2021-11-10 /pmc/articles/PMC8623458/ /pubmed/34835785 http://dx.doi.org/10.3390/nano11113018 Text en © 2021 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
Pierce, Kyle M.
Miklavcic, William R.
Cook, Kyle P.
Hennen, Mikayla Sweitzer
Bayles, Kenneth W.
Hollingsworth, Michael A.
Brooks, Amanda E.
Pullan, Jessica E.
Dailey, Kaitlin M.
The Evolution and Future of Targeted Cancer Therapy: From Nanoparticles, Oncolytic Viruses, and Oncolytic Bacteria to the Treatment of Solid Tumors
title The Evolution and Future of Targeted Cancer Therapy: From Nanoparticles, Oncolytic Viruses, and Oncolytic Bacteria to the Treatment of Solid Tumors
title_full The Evolution and Future of Targeted Cancer Therapy: From Nanoparticles, Oncolytic Viruses, and Oncolytic Bacteria to the Treatment of Solid Tumors
title_fullStr The Evolution and Future of Targeted Cancer Therapy: From Nanoparticles, Oncolytic Viruses, and Oncolytic Bacteria to the Treatment of Solid Tumors
title_full_unstemmed The Evolution and Future of Targeted Cancer Therapy: From Nanoparticles, Oncolytic Viruses, and Oncolytic Bacteria to the Treatment of Solid Tumors
title_short The Evolution and Future of Targeted Cancer Therapy: From Nanoparticles, Oncolytic Viruses, and Oncolytic Bacteria to the Treatment of Solid Tumors
title_sort evolution and future of targeted cancer therapy: from nanoparticles, oncolytic viruses, and oncolytic bacteria to the treatment of solid tumors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623458/
https://www.ncbi.nlm.nih.gov/pubmed/34835785
http://dx.doi.org/10.3390/nano11113018
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