Evidence map›Paper›PMID 21880978›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

The process of macrophage migration promotes matrix metalloproteinase-independent invasion by tumor cells.

Romain Guiet, Emeline Van Goethem, Céline Cougoule, Stéphanie Balor, Annie Valette, Talal Al Saati, Clifford A Lowell, Véronique Le Cabec, Isabelle Maridonneau-Parini

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

52 citing papers in PubMed, 97 citations in OpenAlex.

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  15. Multicellular 3D Models to Study Tumour-Stroma Interactions.International journal of molecular sciences · 2021
    Review
  16. Article
  17. Research progress of tumor microenvironment and tumor-associated macrophages.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
    Review
  18. Organoids as ComplexCellular and molecular bioengineering · 2020
    Review
  19. Article
  20. Article
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

9 authors at 7 institutions in 3 countries.

Romain GuietCentre National de la Recherche Scientifique, Institut de Pharmacologie et de Biologie Structurale, Unité Mixte de Recherche 5089, 31077 Toulouse, France.
Emeline Van Goethem
Céline Cougoule
Stéphanie Balor
Annie Valette
Talal Al Saati
Clifford A Lowell
Véronique Le Cabec
Isabelle Maridonneau-Parini
Institut de Pharmacologie et de Biologie Structurale · FRUniversité Fédérale de Toulouse Midi-Pyrénées · FRInserm · FRInstitut de Génomique Fonctionnelle · FRInstitut des Technologies Avancées en sciences du Vivant · FRUniversité Toulouse III - Paul Sabatier · FRUniversity of California, San Francisco · US

Funding

Signaling by Cytoplasmic Tyrosine Kinases in LeukocytesR01AI068150 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOWELL, CLIFFORD A · 2006 to 2016
$3.4M
NIAID NIH HHS R01 AI068150
6 · The paper itself

Abstract

Tumor-associated macrophages are known to amplify the malignant potential of tumors by secreting a variety of cytokines and proteases involved in tumor cell invasion and metastasis, but how these macrophages infiltrate tumors and whether the macrophage migration process facilitates tumor cell invasion remain poorly documented. To address these questions, we used cell spheroids of breast carcinoma SUM159PT cells as an in vitro model of solid tumors. We found that macrophages used both the mesenchymal mode requiring matrix metalloproteinases (MMPs) and the amoeboid migration mode to infiltrate tumor cell spheroids. Whereas individual SUM159PT cells invaded Matrigel using an MMP-dependent mesenchymal mode, when they were grown as spheroids, tumor cells were unable to invade the Matrigel surrounding spheroids. When spheroids were infiltrated or in contact with macrophages, tumor cell invasiveness was restored. It was dependent on the capacity of macrophages to remodel the matrix and migrate in an MMP-independent mesenchymal mode. This effect of macrophages was much reduced when spheroids were infiltrated by Matrigel migration-defective Hck(-/-) macrophages. In the presence of macrophages, SUM159PT migrated into Matrigel in the proximity of macrophages and switched from an MMP-dependent mesenchymal migration to an amoeboid mode resistant to protease inhibitors.Thus, in addition to the well-described paracrine loop between macrophages and tumor cells, macrophages can also contribute to the invasiveness of tumor cells by remodeling the extracellular matrix and by opening the way to exit the tumor and colonize the surrounding tissues in an MMP-dispensable manner.

Indexed as

AnimalsCell Line, TumorChemotaxis, LeukocyteFemaleHumansImmunohistochemistryMacrophagesMatrix MetalloproteinasesMiceMicroscopy, Electron, ScanningMicroscopy, Electron, TransmissionNeoplasm InvasivenessSpheroids, CellularMatrix Metalloproteinases

Identifiers

PMID21880978
PMCPMC4276309
OpenAlexW2098301447

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.