Evidence map›Paper›PMID 42155037›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2026

Late gestational exposure to flutamide alters stromal composition and immune landscape in the rat mammary gland during pre-puberty, peri-puberty, and adulthood.

David Tovar Parra, Alec McDermott, Jysiane Cardot, Melany Nicole Juarez, Fabien Joao, Rhizlane El Omri-Charai, Line Berthiaume, Bhawna Dhawan, Arash Aghigh, Yann Breton and 5 more

Abstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

David Tovar ParraInstitut National de la Recherche Scientifique (INRS), Centre Armand-Frappier Santé Biotechnologie , 531 boul des Prairies, Laval, Quebec, H7V 1B7, Canada.ORCID 0000-0002-1005-4526
Alec McDermottInstitut National de la Recherche Scientifique (INRS), Centre Armand-Frappier Santé Biotechnologie , 531 boul des Prairies, Laval, Quebec, H7V 1B7, Canada.
Jysiane CardotInstitut National de la Recherche Scientifique (INRS), Centre Armand-Frappier Santé Biotechnologie , 531 boul des Prairies, Laval, Quebec, H7V 1B7, Canada.
Melany Nicole JuarezInstitut National de la Recherche Scientifique (INRS), Centre Armand-Frappier Santé Biotechnologie , 531 boul des Prairies, Laval, Quebec, H7V 1B7, Canada.
Fabien JoaoInstitut National de la Recherche Scientifique (INRS), Centre Armand-Frappier Santé Biotechnologie , 531 boul des Prairies, Laval, Quebec, H7V 1B7, Canada.
Rhizlane El Omri-CharaiInstitut National de la Recherche Scientifique (INRS), Centre Armand-Frappier Santé Biotechnologie , 531 boul des Prairies, Laval, Quebec, H7V 1B7, Canada.
Line BerthiaumeAxe Endocrinologie-Néphrologie, Centre de recherche du CHU de Québec-Université Laval, Québec City, Québec, G1V 4G2, Canada.
Bhawna DhawanCentre Énergie Matériaux Télécommunications, Institut National de la Recherche Scientifique, 1650 boulevard Lionel-Boulet, Varennes, Quebec, J3X 1P7, Canada.
Arash AghighCentre Énergie Matériaux Télécommunications, Institut National de la Recherche Scientifique, 1650 boulevard Lionel-Boulet, Varennes, Quebec, J3X 1P7, Canada.
Yann BretonAxe Maladies infectieuses et immunitaires, Centre de recherche du CHU de Québec-Université Laval, Québec City, Québec, G1V 4G2, Canada.
François LégaréCentre Énergie Matériaux Télécommunications, Institut National de la Recherche Scientifique, 1650 boulevard Lionel-Boulet, Varennes, Quebec, J3X 1P7, Canada.
Géraldine DelbèsInstitut National de la Recherche Scientifique (INRS), Centre Armand-Frappier Santé Biotechnologie , 531 boul des Prairies, Laval, Quebec, H7V 1B7, Canada.ORCID 0000-0002-9169-1075
Martin PelletierAxe Maladies infectieuses et immunitaires, Centre de recherche du CHU de Québec-Université Laval, Québec City, Québec, G1V 4G2, Canada.ORCID 0000-0001-5033-4947
Étienne Audet-WalshAxe Endocrinologie-Néphrologie, Centre de recherche du CHU de Québec-Université Laval, Québec City, Québec, G1V 4G2, Canada.
Isabelle PlanteInstitut National de la Recherche Scientifique (INRS), Centre Armand-Frappier Santé Biotechnologie , 531 boul des Prairies, Laval, Quebec, H7V 1B7, Canada.ORCID 0000-0003-2080-6450

Funding

Fonds de recherche du Québec-Nature et TehnologiesNational Sciences and Engineering Research Council of Canada RGPIN-2019-04740National Sciences and Engineering Research Council of Canada RGPIN-2020-05726National Sciences and Engineering Research Council of Canada RGPIN-2023-0523
6 · The paper itself

Abstract

Perinatal development of the mammary gland is regulated by hormonal signals that influence cell proliferation, extracellular matrix remodeling, immune cell recruitment, and intracellular signaling. Although the role of estrogen in mammary gland development is well established, the impact of androgens remains less understood. To address this gap, we inhibited androgen signaling in utero using the anti-androgen flutamide (FLU) and investigated the effects on mammary gland development in rats. Using an integrative strategy combining histology, transcriptomics, lipidomics, cytokine profiling, and high-resolution imaging, mammary tissue were analyzed at pre-puberty (postnatal days [PND] 21), peri-puberty (PND46), and adulthood (PND90). FLU exposure induced subtle, yet significant, alterations in mammary morphology and molecular signatures. At PND21, the FLU-exposed group exhibited an increased number of adipocytes with reduced size. Transcriptomic analysis revealed differentially expressed genes at PND21 and enrichment in pathways related to androgen response and immune signaling, but minimal changes at later developmental stages. Lipidomic profiling showed transient disruption in long-chain fatty acid composition at early developmental stages. Cytokine profiling revealed a reduced adaptive immune response at PND46 and PND90, and second-harmonic generation imaging demonstrated changes in collagen fiber orientation and density across all developmental stages. These data indicate that prenatal androgen signaling is essential for proper stromal development and the establishment of early transcriptional networks in the mammary gland, with only minor long-term effects on glandular architecture in adult nulliparous females.

Indexed as

Androgen AntagonistsFlutamideMammary Glands, AnimalPrenatal Exposure Delayed EffectsSexual MaturationStromal CellsAnimalsCytokinesFemalePregnancyRatsRats, Sprague-DawleyTranscriptomeAndrogen AntagonistsCytokinesFlutamideandrogen receptoranti-androgenendocrine disruptionlipidomicmammary gland developmenttranscriptomic

Identifiers

PMID42155037
PMCPMC13220753

What Socratic 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 Socratic graph.