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Functional patient-derived organoid screenings identify MCLA-158 as a therapeutic EGFR × LGR5 bispecific antibody with efficacy in epithelial tumors.

Authors :
Herpers B
Eppink B
James MI
Cortina C
Cañellas-Socias A
Boj SF
Hernando-Momblona X
Glodzik D
Roovers RC
van de Wetering M
Bartelink-Clements C
Zondag-van der Zande V
Mateos JG
Yan K
Salinaro L
Basmeleh A
Fatrai S
Maussang D
Lammerts van Bueren JJ
Chicote I
Serna G
Cabellos L
Ramírez L
Nuciforo P
Salazar R
Santos C
Villanueva A
Stephan-Otto Attolini C
Sancho E
Palmer HG
Tabernero J
Stratton MR
de Kruif J
Logtenberg T
Clevers H
Price LS
Vries RGJ
Batlle E
Throsby M
Source :
Nature cancer [Nat Cancer] 2022 Apr; Vol. 3 (4), pp. 418-436. Date of Electronic Publication: 2022 Apr 25.
Publication Year :
2022

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.<br /> (© 2022. The Author(s), under exclusive licence to Springer Nature America, Inc.)

Details

Language :
English
ISSN :
2662-1347
Volume :
3
Issue :
4
Database :
MEDLINE
Journal :
Nature cancer
Publication Type :
Academic Journal
Accession number :
35469014
Full Text :
https://doi.org/10.1038/s43018-022-00359-0