Evidence map›Paper›PMID 39318179›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Constitutive Androstane Receptor Regulates Germ Cell Homeostasis, Sperm Quality, and Male Fertility via Akt-Foxo1 Pathway.

Mélusine Monrose, Hélène Holota, Guillaume Martinez, Christelle Damon-Soubeyrand, Laura Thirouard, Emmanuelle Martinot, Edwige Battistelli, Angélique de Haze, Stéphanie Bravard, Christelle Tamisier and 7 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

17 authors.

Mélusine MonroseINSERM U1103, Université Clermont Auvergne, CNRS UMR-6293, GReD Institute, Team-Volle, Clermont-Ferrand, F-63001, France.
Hélène HolotaINSERM U1103, Université Clermont Auvergne, CNRS UMR-6293, GReD Institute, Team-Volle, Clermont-Ferrand, F-63001, France.
Guillaume MartinezCHU Grenoble Alpes, UM de Génétique Chromosomique, Grenoble, F-38000, France.
Christelle Damon-SoubeyrandINSERM U1103, Université Clermont Auvergne, CNRS UMR-6293, GReD Institute, Team-Volle, Clermont-Ferrand, F-63001, France.
Laura ThirouardINSERM U1103, Université Clermont Auvergne, CNRS UMR-6293, GReD Institute, Team-Volle, Clermont-Ferrand, F-63001, France.
Emmanuelle MartinotINSERM U1103, Université Clermont Auvergne, CNRS UMR-6293, GReD Institute, Team-Volle, Clermont-Ferrand, F-63001, France.
Edwige BattistelliINSERM U1103, Université Clermont Auvergne, CNRS UMR-6293, GReD Institute, Team-Volle, Clermont-Ferrand, F-63001, France.
Angélique de HazeINSERM U1103, Université Clermont Auvergne, CNRS UMR-6293, GReD Institute, Team-Volle, Clermont-Ferrand, F-63001, France.
Stéphanie BravardINSERM U1103, Université Clermont Auvergne, CNRS UMR-6293, GReD Institute, Team-Volle, Clermont-Ferrand, F-63001, France.
Christelle TamisierINSERM U1103, Université Clermont Auvergne, CNRS UMR-6293, GReD Institute, Team-Volle, Clermont-Ferrand, F-63001, France.
Françoise CairaINSERM U1103, Université Clermont Auvergne, CNRS UMR-6293, GReD Institute, Team-Volle, Clermont-Ferrand, F-63001, France.
Charles CouttonCHU Grenoble Alpes, UM de Génétique Chromosomique, Grenoble, F-38000, France.
Anne-Laure BarbotinCHU Lille, Institut de Biologie de la Reproduction-Spermiologie-CECOS, Lille, F-59000, France.
Angèle BoursierCHU Lille, Institut de Biologie de la Reproduction-Spermiologie-CECOS, Lille, F-59000, France.
Laila LakhalINRAe UMR1331, ToxAlim, University of Toulouse, Toulouse, F-31027, France.
Claude BeaudoinINSERM U1103, Université Clermont Auvergne, CNRS UMR-6293, GReD Institute, Team-Volle, Clermont-Ferrand, F-63001, France.
David H VolleINSERM U1103, Université Clermont Auvergne, CNRS UMR-6293, GReD Institute, Team-Volle, Clermont-Ferrand, F-63001, France.ORCID 0000-0003-0843-0550

Funding

Agence Nationale de la Recherche ANR-21-CE14-0083-02Agence Nationale de la Recherche ANR-22-CE34-007-01Cancer-Inserm C20010CSFondation ARC pour la Recherche sur le Cancer ARCDOC42021020003357Fondation pour la Recherche Médicale FDT202001010780Ligue Contre le Cancer
6 · The paper itself

Abstract

Male sexual function can be disrupted by exposure to exogenous compounds that cause testicular physiological alterations. The constitutive androstane receptor (Car) is a receptor for both endobiotics and xenobiotics involved in detoxification. However, its role in male fertility, particularly in regard to the reprotoxic effects of environmental pollutants, remains unclear. This study aims to investigate the role of the Car signaling pathway in male fertility. In vivo, in vitro, and pharmacological approaches are utilized in wild-type and Car-deficient mouse models. The results indicate that Car inhibition impaired male fertility due to altered sperm quality, specifically histone retention, which is correlated with an increased percentage of dying offspring in utero. The data highlighted interactions among Car, Akt, Foxo1, and histone acetylation. This study demonstrates that Car is crucial in germ cell homeostasis and male fertility. Further research on the Car signaling pathway is necessary to reveal unidentified causes of altered fertility and understand the harmful impact of environmental molecules on male fertility and offspring health.

Indexed as

Constitutive Androstane ReceptorFertilityForkhead Box Protein O1HomeostasisReceptors, Cytoplasmic and NuclearSignal TransductionSpermatozoaAnimalsGerm CellsMaleMiceMice, Inbred C57BLProto-Oncogene Proteins c-aktConstitutive Androstane ReceptorForkhead Box Protein O1Foxo1 protein, mouseProto-Oncogene Proteins c-aktReceptors, Cytoplasmic and Nuclearconstitutive androstane receptorFoxo1repro‐toxicityspermatogoniaxenobiotic

Identifiers

PMID39318179
PMCPMC11578384

What OpenQuestion holds

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Registered trials

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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.