Liver Colonization by Colorectal Cancer Metastases Requires YAP-Controlled Plasticity at the Micrometastatic Stage

Author:

Heinz Maria C.12ORCID,Peters Niek A.3ORCID,Oost Koen C.12ORCID,Lindeboom Rik G.H.24ORCID,van Voorthuijsen Lisa24ORCID,Fumagalli Arianna25,van der Net Mirjam C.1ORCID,de Medeiros Gustavo6ORCID,Hageman Joris H.12ORCID,Verlaan-Klink Ingrid12,Borel Rinkes Inne H.M.7,Liberali Prisca68ORCID,Gloerich Martijn1ORCID,van Rheenen Jacco25,Vermeulen Michiel24,Kranenburg Onno3ORCID,Snippert Hugo J.G.12ORCID

Affiliation:

1. 1Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, the Netherlands.

2. 2Oncode Institute, the Netherlands.

3. 3Division of Imaging and Cancer, University Medical Center Utrecht, Utrecht, the Netherlands.

4. 4Department of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, the Netherlands.

5. 5Department of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, the Netherlands.

6. 6Quantitative Biology, Friedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland.

7. 7Department of Surgery, University Medical Center Utrecht, Utrecht, the Netherlands.

8. 8University of Basel, Basel, Switzerland.

Abstract

Abstract Micrometastases of colorectal cancer can remain dormant for years prior to the formation of actively growing, clinically detectable lesions (i.e., colonization). A better understanding of this step in the metastatic cascade could help improve metastasis prevention and treatment. Here we analyzed liver specimens of patients with colorectal cancer and monitored real-time metastasis formation in mouse livers using intravital microscopy to reveal that micrometastatic lesions are devoid of cancer stem cells (CSC). However, lesions that grow into overt metastases demonstrated appearance of de novo CSCs through cellular plasticity at a multicellular stage. Clonal outgrowth of patient-derived colorectal cancer organoids phenocopied the cellular and transcriptomic changes observed during in vivo metastasis formation. First, formation of mature CSCs occurred at a multicellular stage and promoted growth. Conversely, failure of immature CSCs to generate more differentiated cells arrested growth, implying that cellular heterogeneity is required for continuous growth. Second, early-stage YAP activity was required for the survival of organoid-forming cells. However, subsequent attenuation of early-stage YAP activity was essential to allow for the formation of cell type heterogeneity, while persistent YAP signaling locked micro-organoids in a cellularly homogenous and growth-stalled state. Analysis of metastasis formation in mouse livers using single-cell RNA sequencing confirmed the transient presence of early-stage YAP activity, followed by emergence of CSC and non-CSC phenotypes, irrespective of the initial phenotype of the metastatic cell of origin. Thus, establishment of cellular heterogeneity after an initial YAP-controlled outgrowth phase marks the transition to continuously growing macrometastases. Significance: Characterization of the cell type dynamics, composition, and transcriptome of early colorectal cancer liver metastases reveals that failure to establish cellular heterogeneity through YAP-controlled epithelial self-organization prohibits the outgrowth of micrometastases. See related commentary by LeBleu, p. 1870

Funder

Dutch Cancer Society

ERC Starting Grant

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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