Please use this identifier to cite or link to this item: http://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, Hector 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: http://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))

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