Evidence map›Paper›PMID 19726735›Full record

ArticleBiology of reproduction2010

Progesterone receptor-induced gene expression in primary mouse granulosa cell cultures.

Venkataraman Sriraman, Mala Sinha, JoAnne S Richards

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  5. Archives of endocrinology and metabolism · 2021
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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

3 authors at 2 institutions in 1 country.

Venkataraman SriramanEMD-Serono Research Institute, Rockland, Massachusetts, USA.
Mala Sinha
JoAnne S Richards
Baylor College of Medicine · USThe University of Texas Medical Branch at Galveston · US

Funding

TRANSGENIC MOUSE MODELS TO STUDY OVARIAN FUNCTIONU54HD007495 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI RICHARDS, JOANNE STEWART · 1998 to 2013
$19.9M
UTMB WOMEN'S HEALTH RESEARCH SCHOLARS PROGRAMK12HD052023 · NICHD · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI BERENSON, ABBEY B · 2005 to 2023
$8.1M
LH ACTION IN OVARIAN CELL DIFFERENTIATIONR37HD016229 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI RICHARDS, JOANNE S. · 1998 to 2007
$2.0M
LH ACTION IN OVARIAN CELL DIFFERENTIATIONR01HD016229 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI RICHARDS, JOANNE STEWART · 1985 to 2013
$1.9M
GROWTH AND DIFFERENTIATION IN EUKARYOTEST32HD007495 · NICHD · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI KINTNER, CHRISTOPHER ROBERT · 1995 to 2009
$1.6M
LH Action in Ovarian Cell DifferentiationR56HD016229 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI RICHARDS, JOANNE STEWART · 2008 to 2008
$326k
TRANSGENIC ANIMAL--COREP30HD007495 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI GLASSER, STANLEY R · 1985 to 1997
–
NICHD NIH HHS HD-052023NICHD NIH HHS HD-07495NICHD NIH HHS HD-16229NICHD NIH HHS K12 HD052023NICHD NIH HHS P30 HD007495NICHD NIH HHS R01 HD016229NICHD NIH HHS R37 HD016229NICHD NIH HHS R56 HD016229NICHD NIH HHS T32 HD007495NICHD NIH HHS U54 HD007495
6 · The paper itself

Abstract

The progesterone receptor (PGR) is induced by luteinizing hormone (LH) in granulosa cells of preovulatory follicles, and the PGR-A isoform is essential for ovulation based on the phenotypes of Pgr isoform-specific knockout mice. Although several genes regulated by PGR-A in vivo have been identified, whether these genes are primary targets of PGR-A or if their expression also depends on other signaling molecules that are induced by the LH surge has not been resolved. Therefore, to identify genes that are either induced or repressed by PGR in the absence of LH-mediated signaling cascades, we infected primary cultures of mouse granulosa cells with either PGR-A or PGR-B adenoviral vectors without or with R-5020 as a PGR ligand. Total RNA was extracted from infected cells at 16 h and analyzed by Affymetrix Mouse 430 2.0 microarrays. PGR-A in the presence or absence of ligand significantly induced approximately 50 genes 2-fold or more (local pooled error test at P <or= 0.01). Fewer and different genes were induced by PGR-B in the absence of ligand. Edn1, Apoa1, and Cited1 were primarily regulated by PGR-A as verified by additional RT-PCR analyses, suppression by the PGR antagonist RU486, and the lack of induction by protein kinase A, protein kinase C, or epidermal growth factor (EGF)-like factors pathways. PGR regulation of these genes was confirmed further by gene expression analyses in hormonally primed Pgr mutant mouse ovaries. Because Edn1, Apoa1, and Cited1 are known to regulate angiogenesis, PGR may affect the neovascularization of follicles that is initiated with ovulation.

Indexed as

AdenoviridaeAnimalsApolipoprotein A-IApoptosis Regulatory ProteinsCells, CulturedEndothelin-1FemaleGene ExpressionGene Expression RegulationGenetic VectorsGranulosa CellsHumansLuteinizing HormoneMiceMice, Inbred C57BLMifepristoneApolipoprotein A-IApoptosis Regulatory ProteinsCited1 protein, mouseEndothelin-1Luteinizing HormoneMifepristoneNuclear Proteinsprogesterone receptor Aprogesterone receptor BPromegestoneReceptors, ProgesteroneTrans-Activators

Identifiers

PMID19726735
PMCPMC2809228
OpenAlexW2116671711

What OpenQuestion holds

Textmetadata
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.