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Microtubule inhibitor-based antibody–drug conjugates for cancer therapy

The specificity of monoclonal antibodies represents a potential therapeutic advantage, but their use as single agents in oncology has proven limited to date. The development of antibody-drug conjugates (ADCs) takes advantage of the specificity of the monoclonal antibody and potent cytotoxic effect o...

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Autores principales: Klute, Kelsey, Nackos, Eleni, Tasaki, Shinsuke, Nguyen, Daniel P, Bander, Neil H, Tagawa, Scott T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259504/
https://www.ncbi.nlm.nih.gov/pubmed/25506226
http://dx.doi.org/10.2147/OTT.S46887
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author Klute, Kelsey
Nackos, Eleni
Tasaki, Shinsuke
Nguyen, Daniel P
Bander, Neil H
Tagawa, Scott T
author_facet Klute, Kelsey
Nackos, Eleni
Tasaki, Shinsuke
Nguyen, Daniel P
Bander, Neil H
Tagawa, Scott T
author_sort Klute, Kelsey
collection PubMed
description The specificity of monoclonal antibodies represents a potential therapeutic advantage, but their use as single agents in oncology has proven limited to date. The development of antibody-drug conjugates (ADCs) takes advantage of the specificity of the monoclonal antibody and potent cytotoxic effect of chemotherapy, leading to enhanced cytotoxicity in target cells and limiting toxicity to normal tissue. Microtubules represent a validated oncologic target in a range of tumor types, with a number of anti-microtubule targeting cytotoxic drugs approved for cancer use. The systemic use of potent microtubule-binding agents is limited by their effects in normal cells, which leads to toxicity including myelosuppression and peripheral neuropathy. Linking these agents to monoclonal antibodies may limit toxicity to normal tissues and increase drug concentration in target tissues, also allowing the use of more potent agents which would be too toxic to administer in their unbound form. Two such ADCs have been approved for clinical use and many others are in development. Here we review the characteristics of each of the ADC components that have led to efficacious therapies and discuss some of the tubulin inhibitor-based ADCs in development for cancer therapy.
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spelling pubmed-42595042014-12-12 Microtubule inhibitor-based antibody–drug conjugates for cancer therapy Klute, Kelsey Nackos, Eleni Tasaki, Shinsuke Nguyen, Daniel P Bander, Neil H Tagawa, Scott T Onco Targets Ther Review The specificity of monoclonal antibodies represents a potential therapeutic advantage, but their use as single agents in oncology has proven limited to date. The development of antibody-drug conjugates (ADCs) takes advantage of the specificity of the monoclonal antibody and potent cytotoxic effect of chemotherapy, leading to enhanced cytotoxicity in target cells and limiting toxicity to normal tissue. Microtubules represent a validated oncologic target in a range of tumor types, with a number of anti-microtubule targeting cytotoxic drugs approved for cancer use. The systemic use of potent microtubule-binding agents is limited by their effects in normal cells, which leads to toxicity including myelosuppression and peripheral neuropathy. Linking these agents to monoclonal antibodies may limit toxicity to normal tissues and increase drug concentration in target tissues, also allowing the use of more potent agents which would be too toxic to administer in their unbound form. Two such ADCs have been approved for clinical use and many others are in development. Here we review the characteristics of each of the ADC components that have led to efficacious therapies and discuss some of the tubulin inhibitor-based ADCs in development for cancer therapy. Dove Medical Press 2014-12-03 /pmc/articles/PMC4259504/ /pubmed/25506226 http://dx.doi.org/10.2147/OTT.S46887 Text en © 2014 Klute et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Klute, Kelsey
Nackos, Eleni
Tasaki, Shinsuke
Nguyen, Daniel P
Bander, Neil H
Tagawa, Scott T
Microtubule inhibitor-based antibody–drug conjugates for cancer therapy
title Microtubule inhibitor-based antibody–drug conjugates for cancer therapy
title_full Microtubule inhibitor-based antibody–drug conjugates for cancer therapy
title_fullStr Microtubule inhibitor-based antibody–drug conjugates for cancer therapy
title_full_unstemmed Microtubule inhibitor-based antibody–drug conjugates for cancer therapy
title_short Microtubule inhibitor-based antibody–drug conjugates for cancer therapy
title_sort microtubule inhibitor-based antibody–drug conjugates for cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259504/
https://www.ncbi.nlm.nih.gov/pubmed/25506226
http://dx.doi.org/10.2147/OTT.S46887
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