Evidence map›Paper›PMID 38377195›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Targeting nuclear receptor corepressors for reversible male contraception.

Suk-Hyun Hong, Glenda Castro, Dan Wang, Russell Nofsinger, Maureen Kane, Alexandra Folias, Annette R Atkins, Ruth T Yu, Joseph L Napoli, Paolo Sassone-Corsi and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

4 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
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

14 authors at 5 institutions in 3 countries.

Suk-Hyun HongGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037.
Glenda CastroGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037.
Dan WangGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037.
Russell NofsingerGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037.
Maureen KaneDepartment of Nutritional Sciences and Toxicology, The University of California, Berkeley, CA 94720.
Alexandra FoliasDepartment of Nutritional Sciences and Toxicology, The University of California, Berkeley, CA 94720.
Annette R AtkinsGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037.ORCID 0000-0003-3583-4091
Ruth T YuGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037.ORCID 0000-0002-9527-9627
Joseph L NapoliDepartment of Nutritional Sciences and Toxicology, The University of California, Berkeley, CA 94720.ORCID 0000-0003-3223-4752
Paolo Sassone-CorsiDepartment of Biological Chemistry, Center for Epigenetics and Metabolism, U1233 INSERM, University of California, Irvine, CA 92697.
Dirk G de RooijReproductive Biology Group, Division of Developmental Biology, Department of Biology, Faculty of Science, Utrecht University, 3584 CH Utrecht, The Netherlands.ORCID 0000-0003-3932-4419
Christopher LiddleStorr Liver Centre, The Westmead Institute for Medical Research and Sydney Medical School, University of Sydney, Westmead, NSW 2145, Australia.ORCID 0000-0003-3936-6790
Michael DownesGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037.ORCID 0000-0002-6351-9585
Ronald M EvansGene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, CA 92037.ORCID 0000-0002-9986-5965
Salk Institute for Biological Studies · USUniversity of California, Berkeley · USThe University of Sydney · AUUniversity of California, Irvine · USUtrecht University · NL

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Reuben Shaw · 1985 to 2026
$82.8M
Project 3: The AMPK Autophagy Pathway as a Metabolic Liability in Pancratic Ductal AdenocarcinomaP01CA265762 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI TONY R. HUNTER · 2023 to 2026
$14.6M
Histidine phosphorylation as a new target for cancer therapyR35CA242443 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI HUNTER, TONY R. · 2019 to 2025
$7.5M
Organic nanoparticles for dual MRI-guided therapeutic selection and ovarian cancer drug deliveryR01CA220468 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Jeremiah Allen Johnson · 2017 to 2026
$4.9M
Hormonal Regulation of Mammalian Gene ExpressionR01DK057978 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EVANS, RONALD M · 2021 to 2024
$2.6M
NCI NIH HHS P01 CA265762NCI NIH HHS P30 CA014195NCI NIH HHS R01 CA220468NCI NIH HHS R35 CA242443
6 · The paper itself

Abstract

Despite numerous female contraceptive options, nearly half of all pregnancies are unintended. Family planning choices for men are currently limited to unreliable condoms and invasive vasectomies with questionable reversibility. Here, we report the development of an oral contraceptive approach based on transcriptional disruption of cyclical gene expression patterns during spermatogenesis. Spermatogenesis involves a continuous series of self-renewal and differentiation programs of spermatogonial stem cells (SSCs) that is regulated by retinoic acid (RA)-dependent activation of receptors (RARs), which control target gene expression through association with corepressor proteins. We have found that the interaction between RAR and the corepressor silencing mediator of retinoid and thyroid hormone receptors (SMRT) is essential for spermatogenesis. In a genetically engineered mouse model that negates SMRT-RAR binding (SMRT

Indexed as

DNA-Binding ProteinsRepressor ProteinsAnimalsContraceptionCo-Repressor ProteinsFemaleHumansMaleMiceNuclear Receptor Co-Repressor 1Nuclear Receptor Co-Repressor 2TretinoinCo-Repressor ProteinsDNA-Binding ProteinsNuclear Receptor Co-Repressor 1Nuclear Receptor Co-Repressor 2Repressor ProteinsTretinoinretinoic acid signalingspermatogenesistranscriptional corepression

Identifiers

PMID38377195
PMCPMC10907271
OpenAlexW4391985133

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.