Evidence map›Paper›PMID 34680548›Full record

ArticleBiomedicines2021

LRP-1 Matricellular Receptor Involvement in Triple Negative Breast Cancer Tumor Angiogenesis.

Océane Campion, Jessica Thevenard Devy, Clotilde Billottet, Christophe Schneider, Nicolas Etique, Jean-William Dupuy, Anne-Aurélie Raymond, Camille Boulagnon Rombi, Marie Meunier, El-Hadi Djermoune and 8 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-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

14 citing papers in PubMed, 23 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

18 authors at 2 institutions in 1 country.

Océane CampionUFR Sciences Exactes et Naturelles, Université de Reims Champagne-Ardenne, 51687 Reims, France.
Jessica Thevenard DevyUFR Sciences Exactes et Naturelles, Université de Reims Champagne-Ardenne, 51687 Reims, France.
Clotilde BillottetINSERM, LAMC, U1029, Université de Bordeaux, 33600 Pessac, France.
Christophe SchneiderUFR Sciences Exactes et Naturelles, Université de Reims Champagne-Ardenne, 51687 Reims, France.ORCID 0000-0002-7867-0579
Nicolas EtiqueUFR Sciences Exactes et Naturelles, Université de Reims Champagne-Ardenne, 51687 Reims, France.ORCID 0000-0001-6613-9257
Jean-William DupuyPlateforme Protéome, Université de Bordeaux, 33076 Bordeaux, France.ORCID 0000-0002-2448-4797
Anne-Aurélie RaymondPlateforme Oncoprot, TBM-Core US 005, 33000 Bordeaux, France.
Camille Boulagnon RombiMatrice Extracellulaire et Dynamique Cellulaire, MEDyC, UMR 7369 CNRS, 51687 Reims, France.ORCID 0000-0001-5610-1722
Marie MeunierUFR Sciences Exactes et Naturelles, Université de Reims Champagne-Ardenne, 51687 Reims, France.
El-Hadi DjermouneCNRS, CRAN, Université de Lorraine, 54000 Nancy, France.ORCID 0000-0001-6605-2928
Elodie LelièvreUFR Sciences Exactes et Naturelles, Université de Reims Champagne-Ardenne, 51687 Reims, France.
Amandine WahartUFR Sciences Exactes et Naturelles, Université de Reims Champagne-Ardenne, 51687 Reims, France.
Camille BourUFR Sciences Exactes et Naturelles, Université de Reims Champagne-Ardenne, 51687 Reims, France.
Cathy HachetUFR Sciences Exactes et Naturelles, Université de Reims Champagne-Ardenne, 51687 Reims, France.
Stefano CairoXentech, 91000 Evry-Courcouronnes, France.
Andréas BikfalviINSERM, LAMC, U1029, Université de Bordeaux, 33600 Pessac, France.
Stéphane DedieuUFR Sciences Exactes et Naturelles, Université de Reims Champagne-Ardenne, 51687 Reims, France.
Jérôme DevyUFR Sciences Exactes et Naturelles, Université de Reims Champagne-Ardenne, 51687 Reims, France.ORCID 0000-0003-2703-8167
Centre National de la Recherche Scientifique · FRUniversité de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLRP-1 is a multifunctional scavenger receptor belonging to the LDLR family. Due to its capacity to control pericellular levels of various growth factors and proteases, LRP-1 plays a crucial role in membrane proteome dynamics, which appears decisive for tumor progression.

methodsLRP-1 involvement in a TNBC model was assessed using an RNA interference strategy in MDA-MB-231 cells. In vivo, tumorigenic and angiogenic effects of LRP-1-repressed cells were evaluated using an orthotopic xenograft model and two angiogenic assays (Matrigel

resultsLRP-1 repression in MDA-MB-231 tumors led to a 60% growth delay because of, inter alia, morphological and functional vascular differences, confirmed by angiogenic models. In vitro, the LRP-1-repressed cells secretome restrained HUVECs' angiogenic capabilities. A proteomics analysis revealed that LRP-1 supports tumor growth and angiogenesis by regulating TGF-β signaling and plasminogen/plasmin system.

conclusionsLRP-1, by its wide spectrum of interactions, emerges as an important matricellular player in the control of cancer-signaling events such as angiogenesis, by supporting tumor vascular morphology and functionality.

Indexed as

angiogenesisbreast cancerLRP-1TNBC

Identifiers

PMID34680548
PMCPMC8533426
OpenAlexW3205149084

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.