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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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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. |
format | Online Article Text |
id | pubmed-9661471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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