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Overcoming TRAIL Resistance for Glioblastoma Treatment

The tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) shows a promising therapeutic potential in cancer treatment as it exclusively causes apoptosis in a broad spectrum of cancer cells through triggering the extrinsic apoptosis pathway via binding to cognate death receptors, with...

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Detalles Bibliográficos
Autores principales: Deng, Longfei, Zhai, Xuan, Liang, Ping, Cui, Hongjuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070820/
https://www.ncbi.nlm.nih.gov/pubmed/33919846
http://dx.doi.org/10.3390/biom11040572
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author Deng, Longfei
Zhai, Xuan
Liang, Ping
Cui, Hongjuan
author_facet Deng, Longfei
Zhai, Xuan
Liang, Ping
Cui, Hongjuan
author_sort Deng, Longfei
collection PubMed
description The tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) shows a promising therapeutic potential in cancer treatment as it exclusively causes apoptosis in a broad spectrum of cancer cells through triggering the extrinsic apoptosis pathway via binding to cognate death receptors, with negligible toxicity in normal cells. However, most cancers, including glioblastoma multiforme (GBM), display TRAIL resistance, hindering its application in clinical practice. Recent studies have unraveled novel mechanisms in regulating TRAIL-induced apoptosis in GBM and sought effective combinatorial modalities to sensitize GBM to TRAIL treatment, establishing pre-clinical foundations and the reasonable expectation that the TRAIL/TRAIL death receptor axis could be harnessed to treat GBM. In this review, we will revisit the status quo of the mechanisms of TRAIL resistance and emerging strategies for sensitizing GBM to TRAIL-induced apoptosis and also discuss opportunities of TRAIL-based combinatorial therapies in future clinical use for GBM treatment.
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spelling pubmed-80708202021-04-26 Overcoming TRAIL Resistance for Glioblastoma Treatment Deng, Longfei Zhai, Xuan Liang, Ping Cui, Hongjuan Biomolecules Review The tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) shows a promising therapeutic potential in cancer treatment as it exclusively causes apoptosis in a broad spectrum of cancer cells through triggering the extrinsic apoptosis pathway via binding to cognate death receptors, with negligible toxicity in normal cells. However, most cancers, including glioblastoma multiforme (GBM), display TRAIL resistance, hindering its application in clinical practice. Recent studies have unraveled novel mechanisms in regulating TRAIL-induced apoptosis in GBM and sought effective combinatorial modalities to sensitize GBM to TRAIL treatment, establishing pre-clinical foundations and the reasonable expectation that the TRAIL/TRAIL death receptor axis could be harnessed to treat GBM. In this review, we will revisit the status quo of the mechanisms of TRAIL resistance and emerging strategies for sensitizing GBM to TRAIL-induced apoptosis and also discuss opportunities of TRAIL-based combinatorial therapies in future clinical use for GBM treatment. MDPI 2021-04-14 /pmc/articles/PMC8070820/ /pubmed/33919846 http://dx.doi.org/10.3390/biom11040572 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
Deng, Longfei
Zhai, Xuan
Liang, Ping
Cui, Hongjuan
Overcoming TRAIL Resistance for Glioblastoma Treatment
title Overcoming TRAIL Resistance for Glioblastoma Treatment
title_full Overcoming TRAIL Resistance for Glioblastoma Treatment
title_fullStr Overcoming TRAIL Resistance for Glioblastoma Treatment
title_full_unstemmed Overcoming TRAIL Resistance for Glioblastoma Treatment
title_short Overcoming TRAIL Resistance for Glioblastoma Treatment
title_sort overcoming trail resistance for glioblastoma treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070820/
https://www.ncbi.nlm.nih.gov/pubmed/33919846
http://dx.doi.org/10.3390/biom11040572
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