Please use this identifier to cite or link to this item:
https://hdl.handle.net/2445/191089
Title: | Functional patient-derived organoid screenings identify MCLA-158 as a therapeutic EGFR × LGR5 bispecific antibody with efficacy in epithelial tumors |
Author: | Herpers, Bram Eppink, Berina James, Mark I. Cortina, Carme Cañellas Socias, Adrià Boj, Sylvia F. Hernando Momblona, Xavier Glodzik, Dominik Roovers, Rob C. Wetering, Marc van de Bartelink Clements, Carina Zondag van der Zande, Vanessa García Mateos, Jara Yan, Kuan Salinaro, Lucia Basmeleh, Abdoul Fatrai, Szabolc Maussang, David Lammerts van Bueren, Jeroen J. Chicote, Irene Serna, Garazi Cabellos, Laia Ramírez, Lorena Nuciforo, Paolo Salazar Soler, Ramón Santos, Cristina Villanueva Garatachea, Alberto Attolini, Stephan-Otto Sancho, Elena Palmer, Héctor G. Tabernero Caturla, Josep Stratton, Michael R. Kruif, John de Logtenberg, Ton Clevers, Hans Price, Leo S. Vries, Robert Batlle, Eduard Throsby, Mark |
Keywords: | Càncer colorectal Desenvolupament de medicaments Colorectal cancer Drug development |
Issue Date: | 24-Nov-2022 |
Publisher: | Springer Nature |
Abstract: | Patient-derived organoids (PDOs) recapitulate tumor architecture, contain cancer stem cells and have predictive value supporting personalized medicine. Here we describe a large-scale functional screen of dual-targeting bispecific antibodies (bAbs) on a heterogeneous colorectal cancer PDO biobank and paired healthy colonic mucosa samples. More than 500 therapeutic bAbs generated against Wingless-related integration site (WNT) and receptor tyrosine kinase (RTK) targets were functionally evaluated by high-content imaging to capture the complexity of PDO responses. Our drug discovery strategy resulted in the generation of MCLA-158, a bAb that specifically triggers epidermal growth factor receptor degradation in leucine-rich repeat-containing G-protein-coupled receptor 5-positive (LGR5+) cancer stem cells but shows minimal toxicity toward healthy LGR5+ colon stem cells. MCLA-158 exhibits therapeutic properties such as growth inhibition of KRAS-mutant colorectal cancers, blockade of metastasis initiation and suppression of tumor outgrowth in preclinical models for several epithelial cancer types.© 2022. The Author(s), under exclusive licence to Springer Nature America, Inc. |
Note: | Postprint del document publicat a: https://doi.org/10.1038/s43018-022-00359-0 |
It is part of: | Nature Cancer, 2022, num. 3, p. 418–436 |
URI: | https://hdl.handle.net/2445/191089 |
Related resource: | https://doi.org/10.1038/s43018-022-00359-0 |
ISSN: | 2662-1347 |
Appears in Collections: | Articles publicats en revistes (Institut de Recerca Biomèdica (IRB Barcelona)) Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) |
Files in This Item:
File | Description | Size | Format | |
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Nature Cancer_Herpers_2022_FULL.pdf | 11.44 MB | Adobe PDF | View/Open |
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