Evidence map›Paper›PMID 32782397›Full record

ReviewOncogene2020

The oxytocin receptor signalling system and breast cancer: a critical review.

Huiping Liu, Christian W Gruber, Paul F Alewood, Andreas Möller, Markus Muttenthaler

Open access · hybridAbstract readReview
In one paragraph

Review in Oncogene, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
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  16. Design, synthesis, conformational analysis, and biological activity of CαJournal of enzyme inhibition and medicinal chemistry · 2023
    Article
  17. Article
  18. Article
  19. Article
  20. Roles of the Oxytocin Receptor (OXTR) in Human Diseases.International journal of molecular sciences · 2023
    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 at 4 institutions in 2 countries.

Huiping LiuInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, 4072, Australia.ORCID http://orcid.org/0000-0003-0317-9029
Christian W GruberCenter for Physiology and Pharmacology, Medical University of Vienna, 1090, Vienna, Austria.
Paul F AlewoodInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, 4072, Australia.
Andreas MöllerTumour Microenvironment Laboratory, QIMR Berghofer Medical Research Institute, Herston, QLD 4006, Australia.ORCID http://orcid.org/0000-0002-8618-6998
Markus MuttenthalerInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, 4072, Australia. markus.muttenthaler@univie.ac.at.ORCID http://orcid.org/0000-0003-1996-4646
The University of Queensland · AUMedical University of Vienna · ATQIMR Berghofer Medical Research Institute · AUUniversity of Vienna · AT

Funding

Austrian Science Fund FWF I 3243Austrian Science Fund FWF P 32109
6 · The paper itself

Abstract

Breast cancer is making up one-quarter of all new female cancer cases diagnosed worldwide. Breast cancer surgeries, radiation therapies, cytotoxic chemotherapies and targeted therapies have made significant progress and play a dominant role in breast cancer patient management. However, many challenges remain, including resistance to systemic therapies, tumour recurrence and metastasis. The cyclic neuropeptide oxytocin (OT) elicits a plethora of biological responses via the oxytocin receptor (OTR) in both the central and peripheral nervous system, including social bonding, stress, maternal behaviour, sexual activity, uterus contraction, milk ejection and cancer. As a typical member of the G protein-coupled receptor family, OTR represents also an intriguing target for cancer therapy. There is emerging evidence that OTR plays a role in breast cancer development and progression, and several breast cancer cell lines express OTR. However, despite supporting evidence that OT lowers breast cancer risks, its mechanistic role in breast cancer development and the related signalling pathways are not fully understood. Here, we review the current knowledge of the OT/OTR signalling system in healthy breast tissue as well as in breast cancer, and discuss OTR as a potential therapeutic target for breast cancer management.

Indexed as

Disease SusceptibilitySignal TransductionAnimalsAntineoplastic AgentsBreast NeoplasmsCell Transformation, NeoplasticChemopreventionDisease ManagementDisease Models, AnimalDrug Evaluation, PreclinicalFemaleGene Expression Regulation, NeoplasticHumansLigandsMolecular Targeted TherapyOxytocinAntineoplastic AgentsLigandsOxytocinReceptors, EstrogenReceptors, Oxytocin

Identifiers

PMID32782397
PMCPMC7483001
OpenAlexW3048773279

What OpenQuestion holds

Textmetadata
LicenceTDM
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.