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EpCAM Immunotherapy versus Specific Targeted Delivery of Drugs

The epithelial cell adhesion molecule (EpCAM), or CD326, was one of the first cancer associated biomarkers to be discovered. In the last forty years, this biomarker has been investigated for use in personalized cancer therapy, with the first monoclonal antibody, edrecolomab, being trialled in humans...

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Autores principales: Macdonald, Joanna, Henri, Justin, Roy, Kislay, Hays, Emma, Bauer, Michelle, Veedu, Rakesh Naduvile, Pouliot, Normand, Shigdar, Sarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789369/
https://www.ncbi.nlm.nih.gov/pubmed/29329202
http://dx.doi.org/10.3390/cancers10010019
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author Macdonald, Joanna
Henri, Justin
Roy, Kislay
Hays, Emma
Bauer, Michelle
Veedu, Rakesh Naduvile
Pouliot, Normand
Shigdar, Sarah
author_facet Macdonald, Joanna
Henri, Justin
Roy, Kislay
Hays, Emma
Bauer, Michelle
Veedu, Rakesh Naduvile
Pouliot, Normand
Shigdar, Sarah
author_sort Macdonald, Joanna
collection PubMed
description The epithelial cell adhesion molecule (EpCAM), or CD326, was one of the first cancer associated biomarkers to be discovered. In the last forty years, this biomarker has been investigated for use in personalized cancer therapy, with the first monoclonal antibody, edrecolomab, being trialled in humans more than thirty years ago. Since then, several other monoclonal antibodies have been raised to EpCAM and tested in clinical trials. However, while monoclonal antibody therapy has been investigated against EpCAM for almost 40 years as primary or adjuvant therapy, it has not shown as much promise as initially heralded. In this review, we look at the reasons why and consider alternative targeting options, such as aptamers, to turn this almost ubiquitously expressed epithelial cancer biomarker into a viable target for future personalized therapy.
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spelling pubmed-57893692018-02-02 EpCAM Immunotherapy versus Specific Targeted Delivery of Drugs Macdonald, Joanna Henri, Justin Roy, Kislay Hays, Emma Bauer, Michelle Veedu, Rakesh Naduvile Pouliot, Normand Shigdar, Sarah Cancers (Basel) Review The epithelial cell adhesion molecule (EpCAM), or CD326, was one of the first cancer associated biomarkers to be discovered. In the last forty years, this biomarker has been investigated for use in personalized cancer therapy, with the first monoclonal antibody, edrecolomab, being trialled in humans more than thirty years ago. Since then, several other monoclonal antibodies have been raised to EpCAM and tested in clinical trials. However, while monoclonal antibody therapy has been investigated against EpCAM for almost 40 years as primary or adjuvant therapy, it has not shown as much promise as initially heralded. In this review, we look at the reasons why and consider alternative targeting options, such as aptamers, to turn this almost ubiquitously expressed epithelial cancer biomarker into a viable target for future personalized therapy. MDPI 2018-01-12 /pmc/articles/PMC5789369/ /pubmed/29329202 http://dx.doi.org/10.3390/cancers10010019 Text en © 2018 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
Macdonald, Joanna
Henri, Justin
Roy, Kislay
Hays, Emma
Bauer, Michelle
Veedu, Rakesh Naduvile
Pouliot, Normand
Shigdar, Sarah
EpCAM Immunotherapy versus Specific Targeted Delivery of Drugs
title EpCAM Immunotherapy versus Specific Targeted Delivery of Drugs
title_full EpCAM Immunotherapy versus Specific Targeted Delivery of Drugs
title_fullStr EpCAM Immunotherapy versus Specific Targeted Delivery of Drugs
title_full_unstemmed EpCAM Immunotherapy versus Specific Targeted Delivery of Drugs
title_short EpCAM Immunotherapy versus Specific Targeted Delivery of Drugs
title_sort epcam immunotherapy versus specific targeted delivery of drugs
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789369/
https://www.ncbi.nlm.nih.gov/pubmed/29329202
http://dx.doi.org/10.3390/cancers10010019
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