Evidence map›Paper›PMID 32957524›Full record

ReviewCells2020

Role of GPER-Mediated Signaling in Testicular Functions and Tumorigenesis.

Adele Chimento, Arianna De Luca, Marta Claudia Nocito, Paola Avena, Davide La Padula, Lucia Zavaglia, Vincenzo Pezzi

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.9field-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

25 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. GPER: An Estrogen Receptor Key in Metastasis and Tumoral Microenvironments.International journal of molecular sciences · 2023
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Estrogen Receptors-Mediated Apoptosis in Hormone-Dependent Cancers.International journal of molecular sciences · 2022
    Review
  18. 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

7 authors at 1 institution in 1 country.

Adele ChimentoDepartment of Pharmacy, Health and Nutritional Sciences, 87036 Arcavacata di Rende Cosenza, Italy.
Arianna De LucaDepartment of Pharmacy, Health and Nutritional Sciences, 87036 Arcavacata di Rende Cosenza, Italy.
Marta Claudia NocitoDepartment of Pharmacy, Health and Nutritional Sciences, 87036 Arcavacata di Rende Cosenza, Italy.
Paola AvenaDepartment of Pharmacy, Health and Nutritional Sciences, 87036 Arcavacata di Rende Cosenza, Italy.
Davide La PadulaDepartment of Pharmacy, Health and Nutritional Sciences, 87036 Arcavacata di Rende Cosenza, Italy.
Lucia ZavagliaDepartment of Pharmacy, Health and Nutritional Sciences, 87036 Arcavacata di Rende Cosenza, Italy.
Vincenzo PezziDepartment of Pharmacy, Health and Nutritional Sciences, 87036 Arcavacata di Rende Cosenza, Italy.ORCID 0000-0003-2311-2286
University of Calabria · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Estrogen signaling plays important roles in testicular functions and tumorigenesis. Fifteen years ago, it was discovered that a member of the G protein-coupled receptor family, GPR30, which binds also with high affinity to estradiol and is responsible, in part, for the rapid non-genomic actions of estrogens. GPR30, renamed as GPER, was detected in several tissues including germ cells (spermatogonia, spermatocytes, spermatids) and somatic cells (Sertoli and Leydig cells). In our previous review published in 2014, we summarized studies that evidenced a role of GPER signaling in mediating estrogen action during spermatogenesis and testis development. In addition, we evidenced that GPER seems to be involved in modulating estrogen-dependent testicular cancer cell growth; however, the effects on cell survival and proliferation depend on specific cell type. In this review, we update the knowledge obtained in the last years on GPER roles in regulating physiological functions of testicular cells and its involvement in neoplastic transformation of both germ and somatic cells. In particular, we will focus our attention on crosstalk among GPER signaling, classical estrogen receptors and other nuclear receptors involved in testis physiology regulation.

Indexed as

Gene Expression Regulation, NeoplasticReceptor Cross-TalkCell Transformation, NeoplasticErbB ReceptorsEstradiolHumansLeydig CellsMaleReceptors, EstrogenReceptors, G-Protein-CoupledSertoli CellsSignal TransductionSpermatidsSpermatocytesSpermatogenesisSpermatogoniaEGFR protein, humanErbB ReceptorsEstradiolGPER1 protein, humanReceptors, EstrogenReceptors, G-Protein-Coupledgerm cellsGPERLeydig cellsSertoli cellstelocytestesticular cancertestistestis physiology

Identifiers

PMID32957524
PMCPMC7563107
OpenAlexW3086420063

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.