Evidence map›Paper›PMID 22138749›Full record

ArticleCellular and molecular life sciences : CMLS2012

Revisiting the role of hCG: new regulation of the angiogenic factor EG-VEGF and its receptors.

S Brouillet, P Hoffmann, S Chauvet, A Salomon, S Chamboredon, F Sergent, M Benharouga, J J Feige, N Alfaidy

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
5.5field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 70 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Article
  6. Novel Insights into Prokineticin 1 Role in Pregnancy-related Diseases.International journal of medical sciences · 2024
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Placental Development and Pregnancy-Associated Diseases.Maternal-fetal medicine (Wolters Kluwer Health, Inc.) · 2022
    Review
  13. Review
  14. Article
  15. Article
  16. Follicular fluid estradiol is an improved predictor ofExperimental and therapeutic medicine · 2020
    Article
  17. Article
  18. Prediction of severe ovarian hyperstimulation syndrome in women undergoingThe Journal of international medical research · 2020
    Article
  19. Review
  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

9 authors at 5 institutions in 1 country.

S BrouilletInstitut National de la Santé et de la Recherche Médicale, Unité 1036, Laboratoire Biologie du Cancer et de l'Infection, Grenoble, France.
P Hoffmann
S Chauvet
A Salomon
S Chamboredon
F Sergent
M Benharouga
J J Feige
N Alfaidy
Inserm · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRUniversité Joseph Fourier · FRCentre Hospitalier Universitaire de Grenoble · FRUniversité Grenoble Alpes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endocrine gland-derived vascular endothelial growth factor (EG-VEGF) is an angiogenic factor reported to be specific for endocrine tissues, including the placenta. Its biological activity is mediated via two G protein-coupled receptors, prokineticin receptor 1 (PROKR1) and prokineticin receptor 2 (PROKR2). We have recently shown that (i) EG-VEGF expression peaks between the 8th and 11th weeks of gestation, (ii) its mRNA and protein levels are up-regulated by hypoxia, (iii) EG-VEGF is a negative regulator of trophoblast invasion and (iv) its circulating levels are increased in preeclampsia (PE), the most threatening pathology of pregnancy. Here, we investigated the regulation of the expression of EG-VEGF and its receptors by hCG, a key pregnancy hormone that is also deregulated in PE. During the first trimester of pregnancy, hCG and EG-VEGF exhibit the same pattern of expression, suggesting that EG-VEGF is potentially regulated by hCG. Both placental explants (PEX) and primary cultures of trophoblasts from the first trimester of pregnancy were used to investigate this hypothesis. Our results show that (i) LHCGR, the hCG receptor, is expressed both in cyto- and syncytiotrophoblasts, (ii) hCG increases EG-VEGF, PROKR1 and PROKR2 mRNA and protein expression in a dose- and time-dependent manner, (iii) hCG increases the release of EG-VEGF from PEX conditioned media, (iv) hCG effects are transcriptional and post-transcriptional and (v) the hCG effects are mediated by cAMP via cAMP response elements present in the EG-VEGF promoter region. Altogether, these results demonstrate a new role for hCG in the regulation of EG-VEGF and its receptors, an emerging regulatory system in placental development.

Indexed as

Base SequenceCells, CulturedChorionic GonadotropinDNA PrimersFemaleGene ExpressionHumansIn Vitro TechniquesModels, BiologicalMolecular Sequence DataPlacentaPlacentationPregnancyPregnancy Trimester, FirstReceptors, G-Protein-CoupledReceptors, LHChorionic GonadotropinDNA PrimersPROKR1 protein, humanPROKR2 protein, humanReceptors, G-Protein-CoupledReceptors, LHReceptors, PeptideRNA, MessengerVascular Endothelial Growth Factor, Endocrine-Gland-Derived

Identifiers

PMID22138749
PMCPMC11115148
OpenAlexW1978394890

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.