Evidence map›Paper›PMID 32825056›Full record

ArticleCancers2020

P2X7 Receptor Promotes Mouse Mammary Cancer Cell Invasiveness and Tumour Progression, and Is a Target for Anticancer Treatment.

Lucie Brisson, Stéphanie Chadet, Osbaldo Lopez-Charcas, Bilel Jelassi, David Ternant, Julie Chamouton, Stéphanie Lerondel, Alain Le Pape, Isabelle Couillin, Aurélie Gombault and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  9. Targeting purine metabolism in ovarian cancer.Journal of ovarian research · 2022
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  16. P2X7 receptor: a critical regulator and potential target for breast cancer.Journal of molecular medicine (Berlin, Germany) · 2021
    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

15 authors at 3 institutions in 3 countries.

Lucie BrissonInserm UMR1069-Nutrition, Growth and Cancer, University of Tours, 37032 Tours, France.ORCID 0000-0001-7811-1382
Stéphanie ChadetEA4245-Transplantation, Immunology and Inflammation, University of Tours, 37032 Tours, France.
Osbaldo Lopez-CharcasEA4245-Transplantation, Immunology and Inflammation, University of Tours, 37032 Tours, France.ORCID 0000-0002-5080-8310
Bilel JelassiEA4245-Transplantation, Immunology and Inflammation, University of Tours, 37032 Tours, France.
David TernantEA4245-Transplantation, Immunology and Inflammation, University of Tours, 37032 Tours, France.
Julie ChamoutonInserm UMR1069-Nutrition, Growth and Cancer, University of Tours, 37032 Tours, France.
Stéphanie LerondelCNRS UPS44 TAAM, PHENOMIN, Centre d'Imagerie du Petit Animal, 45071 Orléans, France.
Alain Le PapeCNRS UPS44 TAAM, PHENOMIN, Centre d'Imagerie du Petit Animal, 45071 Orléans, France.
Isabelle CouillinLaboratory of Molecular and Experimental Immunology and Neurogenetics, UMR 7355, CNRS, University of Orléans, 45071 Orléans, France.
Aurélie GombaultLaboratory of Molecular and Experimental Immunology and Neurogenetics, UMR 7355, CNRS, University of Orléans, 45071 Orléans, France.
Fabrice TroveroKey-Obs: Preclinical CRO, 45100 Orléans, France.
Stéphan ChevalierInserm UMR1069-Nutrition, Growth and Cancer, University of Tours, 37032 Tours, France.
Pierre BessonEA4245-Transplantation, Immunology and Inflammation, University of Tours, 37032 Tours, France.ORCID 0000-0003-1257-8005
Lin-Hua JiangEA4245-Transplantation, Immunology and Inflammation, University of Tours, 37032 Tours, France.ORCID 0000-0001-6398-0411
Sébastien RogerEA4245-Transplantation, Immunology and Inflammation, University of Tours, 37032 Tours, France.ORCID 0000-0002-9852-5248
Université de Tours · FRCentre National de la Recherche Scientifique · FRUniversité d'Orléans · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The P2X7 receptor is an ATP-gated cation channel with a still ambiguous role in cancer progression, proposed to be either pro- or anti-cancerous, depending on the cancer or cell type in the tumour. Its role in mammary cancer progression is not yet defined. Here, we show that P2X7 receptor is functional in highly aggressive mammary cancer cells, and induces a change in cell morphology with fast F-actin reorganization and formation of filopodia, and promotes cancer cell invasiveness through both 2- and 3-dimensional extracellular matrices in vitro. Furthermore, P2X7 receptor sustains Cdc42 activity and the acquisition of a mesenchymal phenotype. In an immunocompetent mouse mammary cancer model, we reveal that the expression of P2X7 receptor in cancer cells, but not in the host mice, promotes tumour growth and metastasis development, which were reduced by treatment with specific P2X7 antagonists. Our results demonstrate that P2X7 receptor drives mammary tumour progression and represents a pertinent target for mammary cancer treatment.

Indexed as

antagonistscancer cell invasivenessinvadopodiametastasesP2X7 receptor

Identifiers

PMID32825056
PMCPMC7565976
OpenAlexW3058891854

What Socratic 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 Socratic graph.