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Organoid cultures of early-onset colorectal cancers reveal distinct and rare genetic profiles.
- Source :
-
Gut [Gut] 2020 Dec; Vol. 69 (12), pp. 2165-2179. Date of Electronic Publication: 2020 Mar 26. - Publication Year :
- 2020
-
Abstract
- Objective: Sporadic early-onset colorectal cancer (EOCRC) has bad prognosis, yet is poorly represented by cell line models. We examine the key mutational and transcriptomic alterations in an organoid biobank enriched in EOCRCs.<br />Design: We established paired cancer (n=32) and normal organoids (n=18) from 20 patients enriched in microsatellite-stable EOCRC. Exome and transcriptome analysis was performed.<br />Results: We observed a striking diversity of molecular phenotypes, including PTPRK-RSPO3 fusions. Transcriptionally, RSPO fusion organoids resembled normal colon organoids and were distinct from APC mutant organoids, with high BMP2 and low PTK7 expression. Single cell transcriptome analysis confirmed the similarity between RSPO fusion organoids and normal organoids, with a propensity for maturation on Wnt withdrawal, whereas the APC mutant organoids were locked in progenitor stages. CRISPR/Cas9 engineered mutation of APC in normal human colon organoids led to upregulation of PTK7 protein and suppression of BMP2 , but less so with an engineered RNF43 mutation. The frequent co-occurrence of RSPO fusions with SMAD4 or BMPR1A mutation was confirmed in TCGA database searches. RNF43 mutation was found in organoid from a leukaemia survivor with a novel mutational signature; and organoids with POLE proofreading mutation displayed ultramutation. The cancer organoid genomes were stable over long culture periods, while normal human colon organoids tended to be subject to clonal dominance over time.<br />Conclusions: These organoid models enriched in EOCRCs with linked genomic data fill a gap in existing CRC models and reveal distinct genetic profiles and novel pathway cooperativity.<br />Competing Interests: Competing interests: SYL and STY have received research sponsorship from Pfizer, Merck, Servier and Curegenix. HC is an inventor on several patents relating to Wnt activity in cancers and a pending patent on growing organoids from patients with colorectal cancer. He is a cofounder and SAB member of Surrozen, a start-up in Silicon Valley; a SAB member of Kallyope (New York), Merus (Utrecht) and Decibel (Boston); a non-executive board member of Roche (Basel) and SAB member of the Roche subsidiary Genentech (San Francisco) since 2019; a scientific advisor for and investor in Life Sciences Partners, a biotech venture capital firm located in Amsterdam.<br /> (© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.)
- Subjects :
- Adenomatous Polyposis Coli Protein genetics
Bone Morphogenetic Protein 2 genetics
Bone Morphogenetic Protein Receptors, Type I genetics
CRISPR-Cas Systems
Cell Adhesion Molecules genetics
Gene Expression Profiling
Gene Fusion
Humans
Models, Genetic
Mutation
Receptor Protein-Tyrosine Kinases genetics
Receptor-Like Protein Tyrosine Phosphatases, Class 2 genetics
Smad4 Protein genetics
Thrombospondins genetics
Tissue Banks
Ubiquitin-Protein Ligases genetics
Up-Regulation
Exome Sequencing
Colorectal Neoplasms genetics
Genetic Profile
Organoids pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1468-3288
- Volume :
- 69
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Gut
- Publication Type :
- Academic Journal
- Accession number :
- 32217638
- Full Text :
- https://doi.org/10.1136/gutjnl-2019-320019