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A GPC2 antibody-drug conjugate is efficacious against neuroblastoma and small-cell lung cancer via binding a conformational epitope

Glypican 2 (GPC2) is a MYCN-regulated, differentially expressed cell-surface oncoprotein and target for immune-based therapies in neuroblastoma. Here, we build on GPC2’s immunotherapeutic attributes by finding that it is also a highly expressed, MYCN-driven oncoprotein on small-cell lung cancers (SC...

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Autores principales: Raman, Swetha, Buongervino, Samantha N., Lane, Maria V., Zhelev, Doncho V., Zhu, Zhongyu, Cui, Hong, Martinez, Benjamin, Martinez, Daniel, Wang, Yanping, Upton, Kristen, Patel, Khushbu, Rathi, Komal S., Navia, Carmen T., Harmon, Daniel B., Li, Yimei, Pawel, Bruce, Dimitrov, Dimiter S., Maris, John M., Julien, Jean-Philippe, Bosse, Kristopher R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8324494/
https://www.ncbi.nlm.nih.gov/pubmed/34337560
http://dx.doi.org/10.1016/j.xcrm.2021.100344
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author Raman, Swetha
Buongervino, Samantha N.
Lane, Maria V.
Zhelev, Doncho V.
Zhu, Zhongyu
Cui, Hong
Martinez, Benjamin
Martinez, Daniel
Wang, Yanping
Upton, Kristen
Patel, Khushbu
Rathi, Komal S.
Navia, Carmen T.
Harmon, Daniel B.
Li, Yimei
Pawel, Bruce
Dimitrov, Dimiter S.
Maris, John M.
Julien, Jean-Philippe
Bosse, Kristopher R.
author_facet Raman, Swetha
Buongervino, Samantha N.
Lane, Maria V.
Zhelev, Doncho V.
Zhu, Zhongyu
Cui, Hong
Martinez, Benjamin
Martinez, Daniel
Wang, Yanping
Upton, Kristen
Patel, Khushbu
Rathi, Komal S.
Navia, Carmen T.
Harmon, Daniel B.
Li, Yimei
Pawel, Bruce
Dimitrov, Dimiter S.
Maris, John M.
Julien, Jean-Philippe
Bosse, Kristopher R.
author_sort Raman, Swetha
collection PubMed
description Glypican 2 (GPC2) is a MYCN-regulated, differentially expressed cell-surface oncoprotein and target for immune-based therapies in neuroblastoma. Here, we build on GPC2’s immunotherapeutic attributes by finding that it is also a highly expressed, MYCN-driven oncoprotein on small-cell lung cancers (SCLCs), with significantly enriched expression in both the SCLC and neuroblastoma stem cell compartment.By solving the crystal structure of the D3-GPC2-Fab/GPC2 complex at 3.3 Å resolution, we further illustrate that the GPC2-directed antibody-drug conjugate (ADC; D3-GPC2-PBD), that links a human GPC2 antibody (D3) to DNA-damaging pyrrolobenzodiazepine (PBD) dimers, binds a tumor-specific, conformation-dependent epitope of the core GPC2 extracellular domain. We then show that this ADC induces durable neuroblastoma and SCLC tumor regression via induction of DNA damage, apoptosis, and bystander cell killing, notably with no signs of ADC-induced in vivo toxicity. These studies provide preclinical data to support the clinical translation of ADCs targeting GPC2.
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spelling pubmed-83244942021-07-31 A GPC2 antibody-drug conjugate is efficacious against neuroblastoma and small-cell lung cancer via binding a conformational epitope Raman, Swetha Buongervino, Samantha N. Lane, Maria V. Zhelev, Doncho V. Zhu, Zhongyu Cui, Hong Martinez, Benjamin Martinez, Daniel Wang, Yanping Upton, Kristen Patel, Khushbu Rathi, Komal S. Navia, Carmen T. Harmon, Daniel B. Li, Yimei Pawel, Bruce Dimitrov, Dimiter S. Maris, John M. Julien, Jean-Philippe Bosse, Kristopher R. Cell Rep Med Article Glypican 2 (GPC2) is a MYCN-regulated, differentially expressed cell-surface oncoprotein and target for immune-based therapies in neuroblastoma. Here, we build on GPC2’s immunotherapeutic attributes by finding that it is also a highly expressed, MYCN-driven oncoprotein on small-cell lung cancers (SCLCs), with significantly enriched expression in both the SCLC and neuroblastoma stem cell compartment.By solving the crystal structure of the D3-GPC2-Fab/GPC2 complex at 3.3 Å resolution, we further illustrate that the GPC2-directed antibody-drug conjugate (ADC; D3-GPC2-PBD), that links a human GPC2 antibody (D3) to DNA-damaging pyrrolobenzodiazepine (PBD) dimers, binds a tumor-specific, conformation-dependent epitope of the core GPC2 extracellular domain. We then show that this ADC induces durable neuroblastoma and SCLC tumor regression via induction of DNA damage, apoptosis, and bystander cell killing, notably with no signs of ADC-induced in vivo toxicity. These studies provide preclinical data to support the clinical translation of ADCs targeting GPC2. Elsevier 2021-07-21 /pmc/articles/PMC8324494/ /pubmed/34337560 http://dx.doi.org/10.1016/j.xcrm.2021.100344 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Raman, Swetha
Buongervino, Samantha N.
Lane, Maria V.
Zhelev, Doncho V.
Zhu, Zhongyu
Cui, Hong
Martinez, Benjamin
Martinez, Daniel
Wang, Yanping
Upton, Kristen
Patel, Khushbu
Rathi, Komal S.
Navia, Carmen T.
Harmon, Daniel B.
Li, Yimei
Pawel, Bruce
Dimitrov, Dimiter S.
Maris, John M.
Julien, Jean-Philippe
Bosse, Kristopher R.
A GPC2 antibody-drug conjugate is efficacious against neuroblastoma and small-cell lung cancer via binding a conformational epitope
title A GPC2 antibody-drug conjugate is efficacious against neuroblastoma and small-cell lung cancer via binding a conformational epitope
title_full A GPC2 antibody-drug conjugate is efficacious against neuroblastoma and small-cell lung cancer via binding a conformational epitope
title_fullStr A GPC2 antibody-drug conjugate is efficacious against neuroblastoma and small-cell lung cancer via binding a conformational epitope
title_full_unstemmed A GPC2 antibody-drug conjugate is efficacious against neuroblastoma and small-cell lung cancer via binding a conformational epitope
title_short A GPC2 antibody-drug conjugate is efficacious against neuroblastoma and small-cell lung cancer via binding a conformational epitope
title_sort gpc2 antibody-drug conjugate is efficacious against neuroblastoma and small-cell lung cancer via binding a conformational epitope
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8324494/
https://www.ncbi.nlm.nih.gov/pubmed/34337560
http://dx.doi.org/10.1016/j.xcrm.2021.100344
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