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: Kyle M. Pierce, William R. Miklavcic, Kyle P. Cook, Mikayla Sweitzer Hennen, Kenneth W. Bayles, Michael A. Hollingsworth, Amanda E. Brooks, Jessica E. Pullan, Kaitlin M. Dailey
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:c19bdbb1ecd94538b9ccb4e2771189482021-11-25T18:31:47ZThe Evolution and Future of Targeted Cancer Therapy: From Nanoparticles, Oncolytic Viruses, and Oncolytic Bacteria to the Treatment of Solid Tumors10.3390/nano111130182079-4991https://doaj.org/article/c19bdbb1ecd94538b9ccb4e2771189482021-11-01T00:00:00Zhttps://www.mdpi.com/2079-4991/11/11/3018https://doaj.org/toc/2079-4991While 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.Kyle M. PierceWilliam R. MiklavcicKyle P. CookMikayla Sweitzer HennenKenneth W. BaylesMichael A. HollingsworthAmanda E. BrooksJessica E. PullanKaitlin M. DaileyMDPI AGarticlenanoparticlesoncolytic virusesoncolytic bacteriaexosomesclinical trialssolid tumorsChemistryQD1-999ENNanomaterials, Vol 11, Iss 3018, p 3018 (2021)
institution DOAJ
collection DOAJ
language EN
topic nanoparticles
oncolytic viruses
oncolytic bacteria
exosomes
clinical trials
solid tumors
Chemistry
QD1-999
spellingShingle nanoparticles
oncolytic viruses
oncolytic bacteria
exosomes
clinical trials
solid tumors
Chemistry
QD1-999
Kyle M. Pierce
William R. Miklavcic
Kyle P. Cook
Mikayla Sweitzer Hennen
Kenneth W. Bayles
Michael A. Hollingsworth
Amanda E. Brooks
Jessica E. Pullan
Kaitlin M. Dailey
The Evolution and Future of Targeted Cancer Therapy: From Nanoparticles, Oncolytic Viruses, and Oncolytic Bacteria to the Treatment of Solid Tumors
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.
format article
author Kyle M. Pierce
William R. Miklavcic
Kyle P. Cook
Mikayla Sweitzer Hennen
Kenneth W. Bayles
Michael A. Hollingsworth
Amanda E. Brooks
Jessica E. Pullan
Kaitlin M. Dailey
author_facet Kyle M. Pierce
William R. Miklavcic
Kyle P. Cook
Mikayla Sweitzer Hennen
Kenneth W. Bayles
Michael A. Hollingsworth
Amanda E. Brooks
Jessica E. Pullan
Kaitlin M. Dailey
author_sort Kyle M. Pierce
title 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_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_sort evolution and future of targeted cancer therapy: from nanoparticles, oncolytic viruses, and oncolytic bacteria to the treatment of solid tumors
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/c19bdbb1ecd94538b9ccb4e277118948
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