Evidence map›Paper›PMID 35570706›Full record

ArticleCancer research2022

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

Maria C Heinz, Niek A Peters, Koen C Oost, Rik G H Lindeboom, Lisa van Voorthuijsen, Arianna Fumagalli, Mirjam C van der Net, Gustavo de Medeiros, Joris H Hageman, Ingrid Verlaan-Klink and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
9.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

51 citing papers in PubMed, 80 citations in OpenAlex.

  1. Stemness in Colon Cancer.Methods in molecular biology (Clifton, N.J.) · 2027
    Article
  2. Niches in cancer: from primary tumors to metastatic disease.Journal of hematology & oncology · 2026
    Review
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  18. Epigenetic Gatekeeping of Intestinal Stem Cell Transformation.bioRxiv : the preprint server for biology · 2026
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 5 institutions in 2 countries.

Maria C Heinz *Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID 0000-0003-2866-9155
Niek A Peters *Division of Imaging and Cancer, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID 0000-0002-1741-4379
Koen C OostCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID 0000-0002-5162-9939
Rik G H Lindeboom *Oncode Institute, the Netherlands.ORCID 0000-0002-3660-504X
Lisa van Voorthuijsen *Oncode Institute, the Netherlands.ORCID 0000-0003-4822-185X
Arianna Fumagalli *Oncode Institute, the Netherlands.
Mirjam C van der NetCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID 0000-0003-1759-8750
Gustavo de MedeirosQuantitative Biology, Friedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland.ORCID 0000-0001-5877-3012
Joris H HagemanCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID 0000-0002-1386-054X
Ingrid Verlaan-KlinkCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, the Netherlands.
Inne H M Borel RinkesDepartment of Surgery, University Medical Center Utrecht, Utrecht, the Netherlands.
Prisca LiberaliQuantitative Biology, Friedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland.ORCID 0000-0003-0695-6081
Martijn GloerichCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID 0000-0002-0034-4642
Jacco van RheenenOncode Institute, the Netherlands.
Michiel VermeulenOncode Institute, the Netherlands.
Onno KranenburgDivision of Imaging and Cancer, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID 0000-0002-2112-4390
Hugo J G SnippertCenter for Molecular Medicine, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID 0000-0002-4189-5213
Utrecht University · NLRadboud University Nijmegen · NLEncontech (Netherlands) · NLFriedrich Miescher Institute · CHUniversity of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Colorectal NeoplasmsLiver NeoplasmsAnimalsHumansMiceNeoplasm MicrometastasisNeoplastic Stem Cells

Identifiers

PMID35570706
PMCPMC9381095
OpenAlexW4280515619

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.