Evidence map›Paper›PMID 30905738›Full record

ArticleStem cell reports2019

Deciphering the Mammary Stem Cell Niche: A Role for Laminin-Binding Integrins.

Mathilde Romagnoli, Stéphanie Cagnet, Aurélie Chiche, Laura Bresson, Sylvain Baulande, Pierre de la Grange, Adèle De Arcangelis, Maaike Kreft, Elisabeth Georges-Labouesse, Arnoud Sonnenberg and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 2 countries.

Mathilde RomagnoliInstitut Curie, PSL Research University, CNRS, UMR144, 26 Rue d'Ulm, 75005 Paris, France; Sorbonne Universités, UPMC Univ Paris 06, 75005 Paris, France.
Stéphanie CagnetInstitut Curie, PSL Research University, CNRS, UMR144, 26 Rue d'Ulm, 75005 Paris, France; Sorbonne Universités, UPMC Univ Paris 06, 75005 Paris, France.
Aurélie ChicheInstitut Curie, PSL Research University, CNRS, UMR144, 26 Rue d'Ulm, 75005 Paris, France; Sorbonne Universités, UPMC Univ Paris 06, 75005 Paris, France.
Laura BressonInstitut Curie, PSL Research University, CNRS, UMR144, 26 Rue d'Ulm, 75005 Paris, France; Sorbonne Universités, UPMC Univ Paris 06, 75005 Paris, France.
Sylvain BaulandeInstitut Curie Genomics of Excellence (ICGex) Platform, Institut Curie, 75005 Paris, France.
Pierre de la GrangeGenoSplice Technology, 75005 Paris, France.
Adèle De ArcangelisInstitut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS UMR 7104/INSERM U1258/Université de Strasbourg, 67404 Illkirch, France.
Maaike KreftDivision of Cell Biology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.
Elisabeth Georges-LabouesseInstitut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS UMR 7104/INSERM U1258/Université de Strasbourg, 67404 Illkirch, France.
Arnoud SonnenbergDivision of Cell Biology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.
Marie-Ange DeugnierInstitut Curie, PSL Research University, CNRS, UMR144, 26 Rue d'Ulm, 75005 Paris, France; Sorbonne Universités, UPMC Univ Paris 06, 75005 Paris, France; Inserm, Paris, 75013 Paris, France.
Karine RaymondInstitut Curie, PSL Research University, CNRS, UMR144, 26 Rue d'Ulm, 75005 Paris, France; Sorbonne Universités, UPMC Univ Paris 06, 75005 Paris, France; Inserm, Paris, 75013 Paris, France.
Marina A GlukhovaInstitut Curie, PSL Research University, CNRS, UMR144, 26 Rue d'Ulm, 75005 Paris, France; Sorbonne Universités, UPMC Univ Paris 06, 75005 Paris, France; Inserm, Paris, 75013 Paris, France.
Marisa M FaraldoInstitut Curie, PSL Research University, CNRS, UMR144, 26 Rue d'Ulm, 75005 Paris, France; Sorbonne Universités, UPMC Univ Paris 06, 75005 Paris, France; Inserm, Paris, 75013 Paris, France. Electronic address: maria-luisa.martin-faraldo@curie.fr.
Centre National de la Recherche Scientifique · FRThe Netherlands Cancer Institute · NLInstitut Curie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Integrins, which bind laminin, a major component of the mammary basement membrane, are strongly expressed in basal stem cell-enriched populations, but their role in controlling mammary stem cell function remains unclear. We found that stem cell activity, as evaluated in transplantation and mammosphere assays, was reduced in mammary basal cells depleted of laminin receptors containing α3- and α6-integrin subunits. This was accompanied by low MDM2 levels, p53 stabilization, and diminished proliferative capacity. Importantly, disruption of p53 function restored the clonogenicity of α3/α6-integrin-depleted mammary basal stem cells, while inhibition of RHO or myosin II, leading to decreased p53 activity, rescued the mammosphere formation. These data suggest that α3/α6-integrin-mediated adhesion plays an essential role in controlling the proliferative potential of mammary basal stem/progenitor cells through myosin II-mediated regulation of p53 and indicate that laminins might be important components of the mammary stem cell niche.

Indexed as

cre-lox gene deletionintegrinlamininmammary glandstem cells

Identifiers

PMID30905738
PMCPMC6450809
OpenAlexW2923372083

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.