Evidence map›Paper›PMID 39936103›Full record

ReviewFrontiers in endocrinology2025

Interaction of GPER-1 with the endocrine signaling axis in breast cancer.

Luis Molina Calistro, Yennyfer Arancibia, Marcela Alejandra Olivera, Sigrid Domke, Rodrigo Flavio Torres

Abstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. GPCR Biased Signaling in Cancer.Handbook of experimental pharmacology · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. 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

5 authors.

Luis Molina CalistroFacultad de Medicina y Ciencia, Universidad San Sebastián, Puerto Montt, Chile.
Yennyfer ArancibiaFacultad de Medicina y Ciencia, Universidad San Sebastián, Puerto Montt, Chile.
Marcela Alejandra OliveraFacultad de Medicina y Ciencia, Universidad San Sebastián, Puerto Montt, Chile.
Sigrid DomkeFacultad de Ciencias para el cuidado de la salud, Universidad San Sebastián, Puerto Montt, Chile.
Rodrigo Flavio TorresFacultad de Medicina y Ciencia, Universidad San Sebastián, Puerto Montt, Chile.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G Protein-Coupled Estrogen Receptor 1 (GPER-1) is a membrane estrogen receptor that has emerged as a key player in breast cancer development and progression. In addition to its direct influence on estrogen signaling, a crucial interaction between GPER-1 and the hypothalamic-pituitary-gonadal (HPG) axis has been evidenced. The novel and complex relationship between GPER-1 and HPG implies a hormonal regulation with important homeostatic effects on general organ development and reproductive tissues, but also on the pathophysiology of cancer, especially breast cancer. Recent research points to a great versatility of GPER-1, interacting with classical estrogen receptors and with signaling pathways related to inflammation. Importantly, through its activation by environmental and synthetic estrogens, GPER-1 is associated with hormone therapy resistance in breast cancer. These findings open new perspectives in the understanding of breast tumor development and raise the possibility of future applications in the design of more personalized and effective therapeutic approaches.

Indexed as

Breast NeoplasmsHypothalamo-Hypophyseal SystemReceptors, EstrogenReceptors, G-Protein-CoupledSignal TransductionAnimalsEstrogensFemaleHumansEstrogensGPER1 protein, humanReceptors, EstrogenReceptors, G-Protein-Coupledbreast cancerendocrine resistanceestrogenGPER-1hypothalamic-pituitary-gonadal axispersonalized medicine

Identifiers

PMID39936103
PMCPMC11811623

What OpenQuestion holds

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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.