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TRAIL in the Treatment of Cancer: From Soluble Cytokine to Nanosystems
SIMPLE SUMMARY: TRAIL is a death ligand cytokine, predominantly used by effector immune cells to kill malignantly transformed cells. Since its discovery, TRAIL has attracted a lot of attention as a promising anticancer drug due to its selective action against cancer cells, promising a safe, low-toxi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600485/ https://www.ncbi.nlm.nih.gov/pubmed/36291908 http://dx.doi.org/10.3390/cancers14205125 |
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author | Alizadeh Zeinabad, Hojjat Szegezdi, Eva |
author_facet | Alizadeh Zeinabad, Hojjat Szegezdi, Eva |
author_sort | Alizadeh Zeinabad, Hojjat |
collection | PubMed |
description | SIMPLE SUMMARY: TRAIL is a death ligand cytokine, predominantly used by effector immune cells to kill malignantly transformed cells. Since its discovery, TRAIL has attracted a lot of attention as a promising anticancer drug due to its selective action against cancer cells, promising a safe, low-toxicity treatment. Despite its promising characteristics, clinical trials have not delivered on this promise, due to issues with the poor in vivo biological activity of recombinant TRAIL formulations. Nanoparticles have the potential to overcome these limitations, and an increasing number of studies have reported very promising preclinical results. Here, we summarize the potential of TRAIL for cancer therapy, and provide a critical assessment of the challenges and the potential of various formulations of nanovehicles designed to date for TRAIL-based cancer therapy. ABSTRACT: The death ligand tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL), a member of the TNF cytokine superfamily, has long been recognized for its potential as a cancer therapeutic due to its low toxicity against normal cells. However, its translation into a therapeutic molecule has not been successful to date, due to its short in vivo half-life associated with insufficient tumor accumulation and resistance of tumor cells to TRAIL-induced killing. Nanotechnology has the capacity to offer solutions to these limitations. This review provides a perspective and a critical assessment of the most promising approaches to realize TRAIL’s potential as an anticancer therapeutic, including the development of fusion constructs, encapsulation, nanoparticle functionalization and tumor-targeting, and discusses the current challenges and future perspectives. |
format | Online Article Text |
id | pubmed-9600485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96004852022-10-27 TRAIL in the Treatment of Cancer: From Soluble Cytokine to Nanosystems Alizadeh Zeinabad, Hojjat Szegezdi, Eva Cancers (Basel) Review SIMPLE SUMMARY: TRAIL is a death ligand cytokine, predominantly used by effector immune cells to kill malignantly transformed cells. Since its discovery, TRAIL has attracted a lot of attention as a promising anticancer drug due to its selective action against cancer cells, promising a safe, low-toxicity treatment. Despite its promising characteristics, clinical trials have not delivered on this promise, due to issues with the poor in vivo biological activity of recombinant TRAIL formulations. Nanoparticles have the potential to overcome these limitations, and an increasing number of studies have reported very promising preclinical results. Here, we summarize the potential of TRAIL for cancer therapy, and provide a critical assessment of the challenges and the potential of various formulations of nanovehicles designed to date for TRAIL-based cancer therapy. ABSTRACT: The death ligand tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL), a member of the TNF cytokine superfamily, has long been recognized for its potential as a cancer therapeutic due to its low toxicity against normal cells. However, its translation into a therapeutic molecule has not been successful to date, due to its short in vivo half-life associated with insufficient tumor accumulation and resistance of tumor cells to TRAIL-induced killing. Nanotechnology has the capacity to offer solutions to these limitations. This review provides a perspective and a critical assessment of the most promising approaches to realize TRAIL’s potential as an anticancer therapeutic, including the development of fusion constructs, encapsulation, nanoparticle functionalization and tumor-targeting, and discusses the current challenges and future perspectives. MDPI 2022-10-19 /pmc/articles/PMC9600485/ /pubmed/36291908 http://dx.doi.org/10.3390/cancers14205125 Text en © 2022 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 Alizadeh Zeinabad, Hojjat Szegezdi, Eva TRAIL in the Treatment of Cancer: From Soluble Cytokine to Nanosystems |
title | TRAIL in the Treatment of Cancer: From Soluble Cytokine to Nanosystems |
title_full | TRAIL in the Treatment of Cancer: From Soluble Cytokine to Nanosystems |
title_fullStr | TRAIL in the Treatment of Cancer: From Soluble Cytokine to Nanosystems |
title_full_unstemmed | TRAIL in the Treatment of Cancer: From Soluble Cytokine to Nanosystems |
title_short | TRAIL in the Treatment of Cancer: From Soluble Cytokine to Nanosystems |
title_sort | trail in the treatment of cancer: from soluble cytokine to nanosystems |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600485/ https://www.ncbi.nlm.nih.gov/pubmed/36291908 http://dx.doi.org/10.3390/cancers14205125 |
work_keys_str_mv | AT alizadehzeinabadhojjat trailinthetreatmentofcancerfromsolublecytokinetonanosystems AT szegezdieva trailinthetreatmentofcancerfromsolublecytokinetonanosystems |