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Discovery of BT8009: A Nectin-4 Targeting Bicycle Toxin Conjugate for the Treatment of Cancer

[Image: see text] Bicycle toxin conjugates (BTCs) are a promising new class of molecules for targeted delivery of toxin payloads into tumors. Herein we describe the discovery of BT8009, a Nectin-4 targeting BTC currently under clinical evaluation. Nectin-4 is overexpressed in multiple tumor types an...

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Autores principales: Mudd, Gemma E., Scott, Heather, Chen, Liuhong, van Rietschoten, Katerine, Ivanova-Berndt, Gabriela, Dzionek, Katarzyna, Brown, Amy, Watcham, Sophie, White, Lewi, Park, Peter U., Jeffrey, Phil, Rigby, Mike, Beswick, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661471/
https://www.ncbi.nlm.nih.gov/pubmed/36204777
http://dx.doi.org/10.1021/acs.jmedchem.2c00065
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author Mudd, Gemma E.
Scott, Heather
Chen, Liuhong
van Rietschoten, Katerine
Ivanova-Berndt, Gabriela
Dzionek, Katarzyna
Brown, Amy
Watcham, Sophie
White, Lewi
Park, Peter U.
Jeffrey, Phil
Rigby, Mike
Beswick, Paul
author_facet Mudd, Gemma E.
Scott, Heather
Chen, Liuhong
van Rietschoten, Katerine
Ivanova-Berndt, Gabriela
Dzionek, Katarzyna
Brown, Amy
Watcham, Sophie
White, Lewi
Park, Peter U.
Jeffrey, Phil
Rigby, Mike
Beswick, Paul
author_sort Mudd, Gemma E.
collection PubMed
description [Image: see text] Bicycle toxin conjugates (BTCs) are a promising new class of molecules for targeted delivery of toxin payloads into tumors. Herein we describe the discovery of BT8009, a Nectin-4 targeting BTC currently under clinical evaluation. Nectin-4 is overexpressed in multiple tumor types and is a clinically validated target for selective delivery of cytotoxic payloads. A Nectin-4 targeting bicyclic peptide was identified by phage display, which showed highly selective binding for Nectin-4 but suffered from low plasma stability and poor physicochemical properties. Multiparameter chemical optimization involving introduction of non-natural amino acids resulted in a lead Bicycle that demonstrated high affinity for Nectin-4, good stability in biological matrices, and a much-improved physicochemical profile. The optimized Bicycle was conjugated to the cytotoxin Monomethyl auristatin E via a cleavable linker to give the targeted drug conjugate BT8009, which demonstrates potent anticancer activity in in vivo rodent models.
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spelling pubmed-96614712022-11-15 Discovery of BT8009: A Nectin-4 Targeting Bicycle Toxin Conjugate for the Treatment of Cancer Mudd, Gemma E. Scott, Heather Chen, Liuhong van Rietschoten, Katerine Ivanova-Berndt, Gabriela Dzionek, Katarzyna Brown, Amy Watcham, Sophie White, Lewi Park, Peter U. Jeffrey, Phil Rigby, Mike Beswick, Paul J Med Chem [Image: see text] Bicycle toxin conjugates (BTCs) are a promising new class of molecules for targeted delivery of toxin payloads into tumors. Herein we describe the discovery of BT8009, a Nectin-4 targeting BTC currently under clinical evaluation. Nectin-4 is overexpressed in multiple tumor types and is a clinically validated target for selective delivery of cytotoxic payloads. A Nectin-4 targeting bicyclic peptide was identified by phage display, which showed highly selective binding for Nectin-4 but suffered from low plasma stability and poor physicochemical properties. Multiparameter chemical optimization involving introduction of non-natural amino acids resulted in a lead Bicycle that demonstrated high affinity for Nectin-4, good stability in biological matrices, and a much-improved physicochemical profile. The optimized Bicycle was conjugated to the cytotoxin Monomethyl auristatin E via a cleavable linker to give the targeted drug conjugate BT8009, which demonstrates potent anticancer activity in in vivo rodent models. American Chemical Society 2022-10-07 2022-11-10 /pmc/articles/PMC9661471/ /pubmed/36204777 http://dx.doi.org/10.1021/acs.jmedchem.2c00065 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Mudd, Gemma E.
Scott, Heather
Chen, Liuhong
van Rietschoten, Katerine
Ivanova-Berndt, Gabriela
Dzionek, Katarzyna
Brown, Amy
Watcham, Sophie
White, Lewi
Park, Peter U.
Jeffrey, Phil
Rigby, Mike
Beswick, Paul
Discovery of BT8009: A Nectin-4 Targeting Bicycle Toxin Conjugate for the Treatment of Cancer
title Discovery of BT8009: A Nectin-4 Targeting Bicycle Toxin Conjugate for the Treatment of Cancer
title_full Discovery of BT8009: A Nectin-4 Targeting Bicycle Toxin Conjugate for the Treatment of Cancer
title_fullStr Discovery of BT8009: A Nectin-4 Targeting Bicycle Toxin Conjugate for the Treatment of Cancer
title_full_unstemmed Discovery of BT8009: A Nectin-4 Targeting Bicycle Toxin Conjugate for the Treatment of Cancer
title_short Discovery of BT8009: A Nectin-4 Targeting Bicycle Toxin Conjugate for the Treatment of Cancer
title_sort discovery of bt8009: a nectin-4 targeting bicycle toxin conjugate for the treatment of cancer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661471/
https://www.ncbi.nlm.nih.gov/pubmed/36204777
http://dx.doi.org/10.1021/acs.jmedchem.2c00065
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