Evidence map›Paper›PMID 41708829›Full record

ArticleNature aging2026

Induction of senescence during postpartum mammary gland involution supports tissue remodeling and promotes postpartum tumorigenesis.

Aurelie Chiche, Lamia Djoual, Elsa Charifou, Shuoyang Wang, Laurianne Temime, Marielle Saclier, Shaoxiang Wang, Jeremy Chantrel, Han Li

Abstract read
In one paragraph

Article in Nature aging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Tissue-resident memory T cells reshapeFrontiers in immunology · 2026
    Review
  5. 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.

Aurelie Chiche *Cellular plasticity in age-related pathologies, Department of Developmental & Stem Cell Biology, CNRS UMR 3738, Université Paris Cité, Institut Pasteur, Paris, France.
Lamia Djoual *Cellular plasticity in age-related pathologies, Department of Developmental & Stem Cell Biology, CNRS UMR 3738, Université Paris Cité, Institut Pasteur, Paris, France.ORCID http://orcid.org/0009-0002-9312-2586
Elsa Charifou *Cellular plasticity in age-related pathologies, Department of Developmental & Stem Cell Biology, CNRS UMR 3738, Université Paris Cité, Institut Pasteur, Paris, France.
Shuoyang WangCellular plasticity in age-related pathologies, Department of Developmental & Stem Cell Biology, CNRS UMR 3738, Université Paris Cité, Institut Pasteur, Paris, France.ORCID http://orcid.org/0009-0008-0446-8395
Laurianne TemimeCellular plasticity in age-related pathologies, Department of Developmental & Stem Cell Biology, CNRS UMR 3738, Université Paris Cité, Institut Pasteur, Paris, France.ORCID http://orcid.org/0009-0006-6101-968X
Marielle SaclierCellular plasticity in age-related pathologies, Department of Developmental & Stem Cell Biology, CNRS UMR 3738, Université Paris Cité, Institut Pasteur, Paris, France.ORCID http://orcid.org/0000-0002-5194-682X
Shaoxiang WangCellular plasticity in age-related pathologies, Department of Developmental & Stem Cell Biology, CNRS UMR 3738, Université Paris Cité, Institut Pasteur, Paris, France.
Jeremy ChantrelCellular plasticity in age-related pathologies, Department of Developmental & Stem Cell Biology, CNRS UMR 3738, Université Paris Cité, Institut Pasteur, Paris, France.ORCID http://orcid.org/0000-0003-4001-0388
Han LiCellular plasticity in age-related pathologies, Department of Developmental & Stem Cell Biology, CNRS UMR 3738, Université Paris Cité, Institut Pasteur, Paris, France. han.li@pasteur.fr.ORCID http://orcid.org/0000-0002-1065-1179

Funding

AFM-Téléthon (French Muscular Dystrophy Association) 22403Agence Nationale de la Recherche (French National Research Agency) ANR-10-LABX-73, ANR-16-CE13-0017, ANR-21-CE13-0006-01, ANR-22-CE16-0015-03Fondation ARC pour la Recherche sur le Cancer (ARC Foundation for Cancer Research) PJA 20181208231
6 · The paper itself

Abstract

Cellular senescence is an evolutionarily conserved stress response that contributes to tissue repair and tumor suppression, yet its accumulation is also linked to aging and disease. Whether physiological senescence can be exploited by oncogenic events to promote tumorigenesis is unknown. Postpartum mammary gland involution is a major adult tissue remodeling event, resembling wound healing, and is closely associated with postpartum breast cancer. Here, we show that during mammary gland involution in mice, a p16

Indexed as

CarcinogenesisCellular SenescenceMammary Glands, AnimalPostpartum PeriodAnimalsCell Transformation, NeoplasticCyclin-Dependent Kinase Inhibitor p16FemaleLactationMiceCyclin-Dependent Kinase Inhibitor p16

Identifiers

PMID41708829
PMCPMC13004681

What OpenQuestion holds

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LicenceCC BY
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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.