Evidence map›Paper›PMID 37834441›Full record

ReviewInternational journal of molecular sciences2023

GPER: An Estrogen Receptor Key in Metastasis and Tumoral Microenvironments.

Ana Carolina Tirado-Garibay, Elba Andrea Falcón-Ruiz, Alejandra Ochoa-Zarzosa, Joel E López-Meza

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. GPCR Biased Signaling in Cancer.Handbook of experimental pharmacology · 2026
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Epigenetic Modulation of Estrogen Receptor Signaling in Ovarian Cancer.International journal of molecular sciences · 2024
    Review
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

4 authors at 1 institution in 1 country.

Ana Carolina Tirado-GaribayCentro Multidisciplinario de Estudios en Biotecnología-FMVZ, Universidad Michoacana de San Nicolás de Hidalgo, Morelia 58893, Mexico.
Elba Andrea Falcón-RuizCentro Multidisciplinario de Estudios en Biotecnología-FMVZ, Universidad Michoacana de San Nicolás de Hidalgo, Morelia 58893, Mexico.ORCID 0000-0001-5887-4550
Alejandra Ochoa-ZarzosaCentro Multidisciplinario de Estudios en Biotecnología-FMVZ, Universidad Michoacana de San Nicolás de Hidalgo, Morelia 58893, Mexico.ORCID 0000-0003-3441-2989
Joel E López-MezaCentro Multidisciplinario de Estudios en Biotecnología-FMVZ, Universidad Michoacana de San Nicolás de Hidalgo, Morelia 58893, Mexico.ORCID 0000-0002-3269-9202
Universidad Michoacana de San Nicolás de Hidalgo · MX

Funding

Coordinación de la Investigación Científica UMSNH CIC 14.5Instituto de Ciencia, Tecnología e Innovación del Estado de Michoacán PICIR 022-2022
6 · The paper itself

Abstract

Estrogens and their role in cancer are well-studied, and some cancer types are classified in terms of their response to them. In recent years, a G protein-coupled estrogen receptor (GPER) has been described with relevance in cancer. GPER is a pleiotropic receptor with tissue-specific activity; in normal tissues, its activation is related to correct development and homeostasis, while in cancer cells, it can be pro- or anti-tumorigenic. Also, GPER replaces estrogen responsiveness in estrogen receptor alpha (ERα)-lacking cancer cell lines. One of the most outstanding activities of GPER is its role in epithelial-mesenchymal transition (EMT), which is relevant for metastasis development. In addition, the presence of this receptor in tumor microenvironment cells contributes to the phenotypic plasticity required for the dissemination and maintenance of tumors. These characteristics suggest that GPER could be a promising therapeutic target for regulating cancer development. This review focuses on the role of GPER in EMT in tumorigenic and associated cells, highlighting its role in relation to the main hallmarks of cancer and possible therapeutic options.

Indexed as

Receptors, EstrogenTumor MicroenvironmentCell ProliferationEstrogensHumansReceptors, G-Protein-CoupledEstrogensGPER1 protein, humanReceptors, EstrogenReceptors, G-Protein-Coupledepithelium–mesenchymal transitionGPERmetastasistherapeutic targettumor microenvironment

Identifiers

PMID37834441
PMCPMC10573234
OpenAlexW4387457752

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.