Evidence map›Paper›PMID 33007268›Full record

ArticleCell2020

Regulation of Collective Metastasis by Nanolumenal Signaling.

Emma D Wrenn, Ami Yamamoto, Breanna M Moore, Yin Huang, Margaux McBirney, Aaron J Thomas, Erin Greenwood, Yuri F Rabena, Habib Rahbar, Savannah C Partridge and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
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  8. Collective migration modes in development, tissue repair and cancer.Nature reviews. Molecular cell biology · 2025
    Review
  9. Article
  10. Molecular principles underlying aggressive cancers.Signal transduction and targeted therapy · 2025
    Review
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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

11 authors at 4 institutions in 2 countries.

Emma D WrennTranslational Research Program, Public Health Sciences and Human Biology Divisions, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Molecular and Cellular Biology Graduate Program, University of Washington, Seattle, WA 98195, USA.
Ami YamamotoTranslational Research Program, Public Health Sciences and Human Biology Divisions, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Molecular and Cellular Biology Graduate Program, University of Washington, Seattle, WA 98195, USA.
Breanna M MooreTranslational Research Program, Public Health Sciences and Human Biology Divisions, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Yin HuangTranslational Research Program, Public Health Sciences and Human Biology Divisions, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Margaux McBirneyTranslational Research Program, Public Health Sciences and Human Biology Divisions, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Aaron J ThomasTranslational Research Program, Public Health Sciences and Human Biology Divisions, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Erin GreenwoodTranslational Research Program, Public Health Sciences and Human Biology Divisions, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Yuri F RabenaTranslational Research Program, Public Health Sciences and Human Biology Divisions, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Breast Specimen Repository, Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Habib RahbarDepartment of Radiology, University of Washington School of Medicine, Seattle Cancer Care Alliance, Seattle, WA 98109, USA.
Savannah C PartridgeDepartment of Radiology, University of Washington School of Medicine, Seattle Cancer Care Alliance, Seattle, WA 98109, USA.
Kevin J CheungTranslational Research Program, Public Health Sciences and Human Biology Divisions, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. Electronic address: kcheung@fredhutch.org.
Fred Hutch Cancer Center · USSeattle Cancer Care Alliance · USUniversity of Washington · USCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZA

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Role of tumor cell cluster-induced signaling in breast cancer metastasisR37CA234488 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Kevin Jon Cheung · 2020 to 2026
$2.8M
NCI NIH HHS P30 CA015704NCI NIH HHS R37 CA234488
6 · The paper itself

Abstract

Collective metastasis is defined as the cohesive migration and metastasis of multicellular tumor cell clusters. Disrupting various cell adhesion genes markedly reduces cluster formation and colonization efficiency, yet the downstream signals transmitted by clustering remain largely unknown. Here, we use mouse and human breast cancer models to identify a collective signal generated by tumor cell clusters supporting metastatic colonization. We show that tumor cell clusters produce the growth factor epigen and concentrate it within nanolumina-intercellular compartments sealed by cell-cell junctions and lined with microvilli-like protrusions. Epigen knockdown profoundly reduces metastatic outgrowth and switches clusters from a proliferative to a collective migratory state. Tumor cell clusters from basal-like 2, but not mesenchymal-like, triple-negative breast cancer cell lines have increased epigen expression, sealed nanolumina, and impaired outgrowth upon nanolumenal junction disruption. We propose that nanolumenal signaling could offer a therapeutic target for aggressive metastatic breast cancers.

Indexed as

AnimalsBreast NeoplasmsCell AdhesionCell Line, TumorCell MovementEpigenEpithelial-Mesenchymal TransitionHumansIntercellular JunctionsMiceNeoplasm MetastasisNeoplastic Cells, CirculatingSignal TransductionTriple Negative Breast NeoplasmsEpigenbasal-like 2 breast cancercollective invasioncollective metastasiscollective signalingCTC clustersepigennanolumenal signalingnanoluminatriple-negative breast cancertumor cell clusters

Identifiers

PMID33007268
PMCPMC7772852
OpenAlexW3089960120

What OpenQuestion holds

Textmetadata
LicenceTDM
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.