Evidence map›Paper›PMID 27328024›Full record

ArticleMolecular and cellular endocrinology2016

Forkhead box O member FOXO1 regulates the majority of follicle-stimulating hormone responsive genes in ovarian granulosa cells.

Maria K Herndon, Nathan C Law, Elyse M Donaubauer, Brandon Kyriss, Mary Hunzicker-Dunn

Abstract read
In one paragraph

Article in Molecular and cellular endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

37 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Rehmannioside D mitigates disease progression in rats with experimental-induced diminished ovarian reserveThe Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2023
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

Maria K HerndonSchool of Molecular Biosciences and the Center for Reproductive Biology, Washington State University, Pullman WA 99163, USA. Electronic address: mkmeyer@vetmed.wsu.edu.
Nathan C LawSchool of Molecular Biosciences and the Center for Reproductive Biology, Washington State University, Pullman WA 99163, USA. Electronic address: nathan_law@vetmed.wsu.edu.
Elyse M DonaubauerSchool of Molecular Biosciences and the Center for Reproductive Biology, Washington State University, Pullman WA 99163, USA. Electronic address: edonaubauer@vetmed.wsu.edu.
Brandon KyrissSchool of Molecular Biosciences and the Center for Reproductive Biology, Washington State University, Pullman WA 99163, USA. Electronic address: kyrissbp@gmail.com.
Mary Hunzicker-DunnSchool of Molecular Biosciences and the Center for Reproductive Biology, Washington State University, Pullman WA 99163, USA. Electronic address: mehd@wsu.edu.
Washington State University · US

Funding

FSH-Stimulated Signals that Regulate Follicular MaturationR01HD062053 · NICHD · WASHINGTON STATE UNIVERSITY · PI HUNZICKER-DUNN, MARY E, NILSON, JOHN H. · 2009 to 2013
$1.5M
Functional Significance of the HIF1 Transcriptome in Granulosa CellsR01HD065859 · NICHD · WASHINGTON STATE UNIVERSITY · PI HUNZICKER-DUNN, MARY E, NILSON, JOHN H. · 2010 to 2014
$1.5M
Molecular Bioscience Graduate Training ProgramT32GM083864 · NIGMS · WASHINGTON STATE UNIVERSITY · PI NILSON, JOHN H. · 2010 to 2014
$646k
NICHD NIH HHS R01 HD062053NICHD NIH HHS R01 HD065859NIGMS NIH HHS T32 GM083864
6 · The paper itself

Abstract

FSH promotes maturation of ovarian follicles. One pathway activated by FSH in granulosa cells (GCs) is phosphatidylinositol-3 kinase/AKT. The AKT target FOXO1 is reported to function primarily as a repressor of FSH genes, including Ccnd2 and Inha. Based on its broad functions in other tissues, we hypothesized that FOXO1 may regulate many more GC genes. We transduced GCs with empty adenovirus or constitutively active FOXO1 followed by treatment with FSH for 24 h, and conducted RNA deep sequencing. Results show that FSH regulates 3772 genes ≥2.0-fold; 60% of these genes are activated or repressed by FOXO1. Pathway Studio Analysis revealed enrichment of genes repressed by FOXO1 in metabolism, signaling, transport, development, and activated by FOXO1 in signaling, cytoskeletal functions, and apoptosis. Gene regulation was verified by q-PCR (eight genes) and ChIP analysis (two genes). We conclude that FOXO1 regulates the majority of FSH target genes in GCs.

Indexed as

AnimalsCells, CulturedFemaleFollicle Stimulating HormoneForkhead Box Protein O1Gene Expression ProfilingGene Expression RegulationGene Regulatory NetworksGranulosa CellsHigh-Throughput Nucleotide SequencingNerve Tissue ProteinsRatsSequence Analysis, RNAFollicle Stimulating HormoneForkhead Box Protein O1Foxo1 protein, ratNerve Tissue ProteinsFollicle-stimulating hormoneFOXO1Granulosa cellsRNA deep sequencing

Identifiers

PMID27328024
PMCPMC4983523
OpenAlexW2427457449

What OpenQuestion holds

Textmetadata
LicenceTDM
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.