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Antibodies and Derivatives Targeting DR4 and DR5 for Cancer Therapy

Developing therapeutics that induce apoptosis in cancer cells has become an increasingly attractive approach for the past 30 years. The discovery of tumor necrosis factor (TNF) superfamily members and more specifically TNF-related apoptosis-inducing ligand (TRAIL), the only cytokine of the family ca...

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Detalles Bibliográficos
Autores principales: Dubuisson, Agathe, Micheau, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698863/
https://www.ncbi.nlm.nih.gov/pubmed/31548531
http://dx.doi.org/10.3390/antib6040016
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author Dubuisson, Agathe
Micheau, Olivier
author_facet Dubuisson, Agathe
Micheau, Olivier
author_sort Dubuisson, Agathe
collection PubMed
description Developing therapeutics that induce apoptosis in cancer cells has become an increasingly attractive approach for the past 30 years. The discovery of tumor necrosis factor (TNF) superfamily members and more specifically TNF-related apoptosis-inducing ligand (TRAIL), the only cytokine of the family capable of eradicating selectively cancer cells, led to the development of numerous TRAIL derivatives targeting death receptor 4 (DR4) and death receptor 5 (DR5) for cancer therapy. With a few exceptions, preliminary attempts to use recombinant TRAIL, agonistic antibodies, or derivatives to target TRAIL agonist receptors in the clinic have been fairly disappointing. Nonetheless, a tremendous effort, worldwide, is being put into the development of novel strategic options to target TRAIL receptors. Antibodies and derivatives allow for the design of novel and efficient agonists. We summarize and discuss here the advantages and drawbacks of the soar of TRAIL therapeutics, from the first developments to the next generation of agonistic products, with a particular insight on new concepts.
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spelling pubmed-66988632019-09-05 Antibodies and Derivatives Targeting DR4 and DR5 for Cancer Therapy Dubuisson, Agathe Micheau, Olivier Antibodies (Basel) Review Developing therapeutics that induce apoptosis in cancer cells has become an increasingly attractive approach for the past 30 years. The discovery of tumor necrosis factor (TNF) superfamily members and more specifically TNF-related apoptosis-inducing ligand (TRAIL), the only cytokine of the family capable of eradicating selectively cancer cells, led to the development of numerous TRAIL derivatives targeting death receptor 4 (DR4) and death receptor 5 (DR5) for cancer therapy. With a few exceptions, preliminary attempts to use recombinant TRAIL, agonistic antibodies, or derivatives to target TRAIL agonist receptors in the clinic have been fairly disappointing. Nonetheless, a tremendous effort, worldwide, is being put into the development of novel strategic options to target TRAIL receptors. Antibodies and derivatives allow for the design of novel and efficient agonists. We summarize and discuss here the advantages and drawbacks of the soar of TRAIL therapeutics, from the first developments to the next generation of agonistic products, with a particular insight on new concepts. MDPI 2017-10-25 /pmc/articles/PMC6698863/ /pubmed/31548531 http://dx.doi.org/10.3390/antib6040016 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Dubuisson, Agathe
Micheau, Olivier
Antibodies and Derivatives Targeting DR4 and DR5 for Cancer Therapy
title Antibodies and Derivatives Targeting DR4 and DR5 for Cancer Therapy
title_full Antibodies and Derivatives Targeting DR4 and DR5 for Cancer Therapy
title_fullStr Antibodies and Derivatives Targeting DR4 and DR5 for Cancer Therapy
title_full_unstemmed Antibodies and Derivatives Targeting DR4 and DR5 for Cancer Therapy
title_short Antibodies and Derivatives Targeting DR4 and DR5 for Cancer Therapy
title_sort antibodies and derivatives targeting dr4 and dr5 for cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698863/
https://www.ncbi.nlm.nih.gov/pubmed/31548531
http://dx.doi.org/10.3390/antib6040016
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