Evidence map›Paper›PMID 27324437›Full record

ArticleScientific reports2016

Protein Kinase A: A Master Kinase of Granulosa Cell Differentiation.

Pawan Puri, Lynda Little-Ihrig, Uma Chandran, Nathan C Law, Mary Hunzicker-Dunn, Anthony J Zeleznik

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 67 citations in OpenAlex.

  1. Review
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  6. Identification of FSH-regulated and estrous stage-specific transcriptional networks in mouse ovaries.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  15. AKAP13 Enhances CREB1 Activation by FSH in Granulosa Cells.Reproductive sciences (Thousand Oaks, Calif.) · 2023
    Article
  16. The role of amphiregulin in ovarian function and disease.Cellular and molecular life sciences : CMLS · 2023
    Review
  17. Review
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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

6 authors at 3 institutions in 1 country.

Pawan PuriDepartment of Obstetrics, Gynecology and Reproductive Sciences, Magee Womens Research Institute, University of Pittsburgh, Pittsburgh, 15213, PA, USA.
Lynda Little-IhrigDepartment of Obstetrics, Gynecology and Reproductive Sciences, Magee Womens Research Institute, University of Pittsburgh, Pittsburgh, 15213, PA, USA.
Uma ChandranDepartment of Biomedical Informatics, University of Pittsburgh, Pittsburgh, 15206, PA, USA.
Nathan C LawSchool of Molecular Biosciences, College of Veterinary Medicine, Washington State University, Pullman, 99164, WA, USA.
Mary Hunzicker-DunnSchool of Molecular Biosciences, College of Veterinary Medicine, Washington State University, Pullman, 99164, WA, USA.
Anthony J ZeleznikDepartment of Obstetrics, Gynecology and Reproductive Sciences, Magee Womens Research Institute, University of Pittsburgh, Pittsburgh, 15213, PA, USA.
Magee-Womens Research Institute · USWashington State University · USUniversity of Pittsburgh · 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
Cyclic AMP Signaling in Granulosa CellsR01HD059901 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ZELEZNIK, ANTHONY J · 2010 to 2013
$1.1M
Molecular Bioscience Graduate Training ProgramT32GM083864 · NIGMS · WASHINGTON STATE UNIVERSITY · PI NILSON, JOHN H. · 2010 to 2014
$646k
NICHD NIH HHS R01 HD059901NICHD NIH HHS R01 HD062053NICHD NIH HHS R01 HD065859NIGMS NIH HHS T32 GM083864
6 · The paper itself

Abstract

Activation of protein kinase A (PKA) by follicle stimulating hormone (FSH) transduces the signal that drives differentiation of ovarian granulosa cells (GCs). An unresolved question is whether PKA is sufficient to initiate the complex program of GC responses to FSH. We compared signaling pathways and gene expression profiles of GCs stimulated with FSH or expressing PKA-CQR, a constitutively active mutant of PKA. Both FSH and PKA-CQR stimulated the phosphorylation of proteins known to be involved in GC differentiation including CREB, ß-catenin, AKT, p42/44 MAPK, GAB2, GSK-3ß, FOXO1, and YAP. In contrast, FSH stimulated the phosphorylation of p38 MAP kinase but PKA-CQR did not. Microarray analysis revealed that 85% of transcripts that were up-regulated by FSH were increased to a comparable extent by PKA-CQR and of the transcripts that were down-regulated by FSH, 76% were also down-regulated by PKA-CQR. Transcripts regulated similarly by FSH and PKA-CQR are involved in steroidogenesis and differentiation, while transcripts more robustly up-regulated by PKA-CQR are involved in ovulation. Thus, PKA, under the conditions of our experimental approach appears to function as a master upstream kinase that is sufficient to initiate the complex pattern of intracellular signaling pathway and gene expression profiles that accompany GC differentiation.

Indexed as

Animalsbeta CateninCell DifferentiationCells, CulturedCyclic AMP-Dependent Protein KinasesFemaleFollicle Stimulating Hormone, HumanGene Expression RegulationGlycogen Synthase Kinase 3Granulosa CellsHumansMutationOvaryp38 Mitogen-Activated Protein KinasesRatsRats, Inbred Strainsbeta CateninCyclic AMP-Dependent Protein KinasesFollicle Stimulating Hormone, HumanGlycogen Synthase Kinase 3p38 Mitogen-Activated Protein KinasesSteroids

Identifiers

PMID27324437
PMCPMC4914995
OpenAlexW2460203703

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.