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Targeting Receptors on Cancer Cells with Protein Toxins

Cancer cells frequently upregulate surface receptors that promote growth and survival. These receptors constitute valid targets for intervention. One strategy involves the delivery of toxic payloads with the goal of killing those cancer cells with high receptor levels. Delivery can be accomplished b...

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Detalles Bibliográficos
Autores principales: Antignani, Antonella, Ho, Eric Chun Hei, Bilotta, Maria Teresa, Qiu, Rong, Sarnvosky, Robert, FitzGerald, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563326/
https://www.ncbi.nlm.nih.gov/pubmed/32957689
http://dx.doi.org/10.3390/biom10091331
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author Antignani, Antonella
Ho, Eric Chun Hei
Bilotta, Maria Teresa
Qiu, Rong
Sarnvosky, Robert
FitzGerald, David J.
author_facet Antignani, Antonella
Ho, Eric Chun Hei
Bilotta, Maria Teresa
Qiu, Rong
Sarnvosky, Robert
FitzGerald, David J.
author_sort Antignani, Antonella
collection PubMed
description Cancer cells frequently upregulate surface receptors that promote growth and survival. These receptors constitute valid targets for intervention. One strategy involves the delivery of toxic payloads with the goal of killing those cancer cells with high receptor levels. Delivery can be accomplished by attaching a toxic payload to either a receptor-binding antibody or a receptor-binding ligand. Generally, the cell-binding domain of the toxin is replaced with a ligand or antibody that dictates a new binding specificity. The advantage of this “immunotoxin” approach lies in the potency of these chimeric molecules for killing cancer cells. However, receptor expression on normal tissue represents a significant obstacle to therapeutic intervention.
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spelling pubmed-75633262020-10-27 Targeting Receptors on Cancer Cells with Protein Toxins Antignani, Antonella Ho, Eric Chun Hei Bilotta, Maria Teresa Qiu, Rong Sarnvosky, Robert FitzGerald, David J. Biomolecules Review Cancer cells frequently upregulate surface receptors that promote growth and survival. These receptors constitute valid targets for intervention. One strategy involves the delivery of toxic payloads with the goal of killing those cancer cells with high receptor levels. Delivery can be accomplished by attaching a toxic payload to either a receptor-binding antibody or a receptor-binding ligand. Generally, the cell-binding domain of the toxin is replaced with a ligand or antibody that dictates a new binding specificity. The advantage of this “immunotoxin” approach lies in the potency of these chimeric molecules for killing cancer cells. However, receptor expression on normal tissue represents a significant obstacle to therapeutic intervention. MDPI 2020-09-17 /pmc/articles/PMC7563326/ /pubmed/32957689 http://dx.doi.org/10.3390/biom10091331 Text en © 2020 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
Antignani, Antonella
Ho, Eric Chun Hei
Bilotta, Maria Teresa
Qiu, Rong
Sarnvosky, Robert
FitzGerald, David J.
Targeting Receptors on Cancer Cells with Protein Toxins
title Targeting Receptors on Cancer Cells with Protein Toxins
title_full Targeting Receptors on Cancer Cells with Protein Toxins
title_fullStr Targeting Receptors on Cancer Cells with Protein Toxins
title_full_unstemmed Targeting Receptors on Cancer Cells with Protein Toxins
title_short Targeting Receptors on Cancer Cells with Protein Toxins
title_sort targeting receptors on cancer cells with protein toxins
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7563326/
https://www.ncbi.nlm.nih.gov/pubmed/32957689
http://dx.doi.org/10.3390/biom10091331
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