Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/191089
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dc.contributor.authorHerpers, Bram-
dc.contributor.authorEppink, Berina-
dc.contributor.authorJames, Mark I.-
dc.contributor.authorCortina, Carme-
dc.contributor.authorCañellas Socias, Adrià-
dc.contributor.authorBoj, Sylvia F.-
dc.contributor.authorHernando Momblona, Xavier-
dc.contributor.authorGlodzik, Dominik-
dc.contributor.authorRoovers, Rob C.-
dc.contributor.authorWetering, Marc van de-
dc.contributor.authorBartelink Clements, Carina-
dc.contributor.authorZondag van der Zande, Vanessa-
dc.contributor.authorGarcía Mateos, Jara-
dc.contributor.authorYan, Kuan-
dc.contributor.authorSalinaro, Lucia-
dc.contributor.authorBasmeleh, Abdoul-
dc.contributor.authorFatrai, Szabolc-
dc.contributor.authorMaussang, David-
dc.contributor.authorLammerts van Bueren, Jeroen J.-
dc.contributor.authorChicote, Irene-
dc.contributor.authorSerna, Garazi-
dc.contributor.authorCabellos, Laia-
dc.contributor.authorRamírez, Lorena-
dc.contributor.authorNuciforo, Paolo-
dc.contributor.authorSalazar Soler, Ramón-
dc.contributor.authorSantos, Cristina-
dc.contributor.authorVillanueva Garatachea, Alberto-
dc.contributor.authorAttolini, Stephan-Otto-
dc.contributor.authorSancho, Elena-
dc.contributor.authorPalmer, Héctor G.-
dc.contributor.authorTabernero Caturla, Josep-
dc.contributor.authorStratton, Michael R.-
dc.contributor.authorKruif, John de-
dc.contributor.authorLogtenberg, Ton-
dc.contributor.authorClevers, Hans-
dc.contributor.authorPrice, Leo S.-
dc.contributor.authorVries, Robert-
dc.contributor.authorBatlle, Eduard-
dc.contributor.authorThrosby, Mark-
dc.date.accessioned2022-11-24T09:30:25Z-
dc.date.available2022-11-24T09:30:25Z-
dc.date.issued2022-11-24-
dc.identifier.issn2662-1347-
dc.identifier.urihttps://hdl.handle.net/2445/191089-
dc.description.abstractPatient-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.-
dc.format.extent36 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSpringer Nature-
dc.relation.isformatofPostprint del document publicat a: https://doi.org/10.1038/s43018-022-00359-0-
dc.relation.ispartofNature Cancer, 2022, num. 3, p. 418–436-
dc.relation.urihttps://doi.org/10.1038/s43018-022-00359-0-
dc.rights(c) Herpers, Bram, 2022-
dc.sourceArticles publicats en revistes (Institut de Recerca Biomèdica (IRB Barcelona))-
dc.subject.classificationCàncer colorectal-
dc.subject.classificationDesenvolupament de medicaments-
dc.subject.otherColorectal cancer-
dc.subject.otherDrug development-
dc.titleFunctional patient-derived organoid screenings identify MCLA-158 as a therapeutic EGFR × LGR5 bispecific antibody with efficacy in epithelial tumors-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.date.updated2022-11-23T12:27:35Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.idimarina6549334-
dc.identifier.pmid35469014-
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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