Evidence map›Paper›PMID 31091437›Full record

ArticleCell reports2019

Integrin-Mediated Macrophage Adhesion Promotes Lymphovascular Dissemination in Breast Cancer.

Rachel Evans, Fabian Flores-Borja, Sina Nassiri, Elena Miranda, Katherine Lawler, Anita Grigoriadis, James Monypenny, Cheryl Gillet, Julie Owen, Peter Gordon and 13 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2019. 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
3.4field-weighted citation impact, top 6% 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, 57 citations in OpenAlex.

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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

23 authors at 5 institutions in 2 countries.

Rachel EvansRichard Dimbleby Department of Cancer Research, Randall Division & Division of Cancer Studies, Kings College London, London, UK. Electronic address: rachel.evans@ucl.ac.uk.
Fabian Flores-BorjaBreast Cancer Now Research Unit, King's College London, Guy's Hospital, London, UK.
Sina NassiriSwiss Institute for Experimental Cancer Research (ISREC), School of Life Sciences, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Elena MirandaPathology Core Facility, University College London Cancer Institute, London, UK.
Katherine LawlerRichard Dimbleby Department of Cancer Research, Randall Division & Division of Cancer Studies, Kings College London, London, UK; Institute for Mathematical and Molecular Biomedicine, King's College London, London, UK.
Anita GrigoriadisBreast Cancer Now Research Unit, King's College London, Guy's Hospital, London, UK.
James MonypennyRichard Dimbleby Department of Cancer Research, Randall Division & Division of Cancer Studies, Kings College London, London, UK.
Cheryl GilletKing's Health Partners Cancer Biobank, King's College London, London, UK; Research Oncology, Division of Cancer Studies, Guy's Hospital, King's College London, London, UK.
Julie OwenKing's Health Partners Cancer Biobank, King's College London, London, UK; Research Oncology, Division of Cancer Studies, Guy's Hospital, King's College London, London, UK.
Peter GordonBreast Cancer Now Research Unit, King's College London, Guy's Hospital, London, UK.
Victoria MaleBreast Cancer Now Research Unit, King's College London, Guy's Hospital, London, UK.
Anthony CheungBreast Cancer Now Research Unit, King's College London, Guy's Hospital, London, UK.
Farzana NoorBreast Cancer Now Research Unit, King's College London, Guy's Hospital, London, UK.
Paul BarberRichard Dimbleby Department of Cancer Research, Randall Division & Division of Cancer Studies, Kings College London, London, UK; UCL Cancer Institute, University College London, London, UK.
Rebecca MarlowBreast Cancer Now Research Unit, King's College London, Guy's Hospital, London, UK.
Erika Francesch-DomenechBreast Cancer Now Research Unit, King's College London, Guy's Hospital, London, UK.
Gilbert FruhwirthDivision of Imaging Sciences and Biomedical Engineering, King's College London, London, UK.
Mario SquadritoSwiss Institute for Experimental Cancer Research (ISREC), School of Life Sciences, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Borivoj VojnovicDepartment of Oncology, Cancer Research UK and Medical Research Council, Oxford Institute for Radiation Oncology, University of Oxford, UK.
Andrew TuttBreast Cancer Now Research Unit, King's College London, Guy's Hospital, London, UK.
Frederic FestyTissue Engineering and Biophotonics, King's College London, London, UK.
Michele De PalmaSwiss Institute for Experimental Cancer Research (ISREC), School of Life Sciences, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Tony NgRichard Dimbleby Department of Cancer Research, Randall Division & Division of Cancer Studies, Kings College London, London, UK; Breast Cancer Now Research Unit, King's College London, Guy's Hospital, London, UK; UCL Cancer Institute, University College London, London, UK. Electronic address: tony.ng@kcl.ac.uk.
Guy's Hospital · GBKing's College London · GBÉcole Polytechnique Fédérale de Lausanne · CHCancer Research UK · GBLondon Cancer · GB

Funding

Cancer Research UK 16463Cancer Research UK 20265Cancer Research UK C1519/A10331Cancer Research UK C1519/A16463Cancer Research UK C1519/A6906Cancer Research UK C5255/A15935
6 · The paper itself

Abstract

Lymphatic vasculature is crucial for metastasis in triple-negative breast cancer (TNBC); however, cellular and molecular drivers controlling lymphovascular metastasis are poorly understood. We define a macrophage-dependent signaling cascade that facilitates metastasis through lymphovascular remodeling. TNBC cells instigate mRNA changes in macrophages, resulting in β4 integrin-dependent adhesion to the lymphovasculature. β4 integrin retains macrophages proximal to lymphatic endothelial cells (LECs), where release of TGF-β1 drives LEC contraction via RhoA activation. Macrophages promote gross architectural changes to lymphovasculature by increasing dilation, hyperpermeability, and disorganization. TGF-β1 drives β4 integrin clustering at the macrophage plasma membrane, further promoting macrophage adhesion and demonstrating the dual functionality of TGF-β1 signaling in this context. β4 integrin-expressing macrophages were identified in human breast tumors, and a combination of vascular-remodeling macrophage gene signature and TGF-β signaling scores correlates with metastasis. We postulate that future clinical strategies for patients with TNBC should target crosstalk between β4 integrin and TGF-β1.

Indexed as

AnimalsCell AdhesionCell Adhesion MoleculesEndothelial CellsFemaleGene Expression Regulation, NeoplasticHEK293 CellsHumansIntegrin beta4KalininLymphatic MetastasisLymphatic VesselsMacrophagesMiceMice, Inbred BALB CMice, Inbred C57BLCell Adhesion MoleculesIntegrin beta4KalininrhoA GTP-Binding ProteinRHOA protein, humanTGFB1 protein, humanTransforming Growth Factor beta1adhesioncancercontractionlymphovasculaturemacrophagesremodelingRhoATGF-β1β4 integrin

Identifiers

PMID31091437
PMCPMC6527923
OpenAlexW2946828413

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.