Evidence map›Paper›PMID 32098331›Full record

ArticleBiology2020

β2-Adrenergic Signalling Promotes Cell Migration by Upregulating Expression of the Metastasis-Associated Molecule LYPD3.

Michael Gruet, Daniel Cotton, Clare Coveney, David J Boocock, Sarah Wagner, Lucie Komorowski, Robert C Rees, A Graham Pockley, A Christopher Garner, John D Wallis and 2 more

Open access · goldAbstract read
In one paragraph

Article in Biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% 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, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. The β2-adrenergic receptor associates with CXCR4 multimers in human cancer cells.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Article
  9. βCells · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. The tumor-nerve circuit in breast cancer.Cancer metastasis reviews · 2023
    Review
  15. Article
  16. ß-Adrenoreceptors in Human Cancers.International journal of molecular sciences · 2023
    Review
  17. Article
  18. Review
  19. Article
  20. 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

12 authors at 2 institutions in 1 country.

Michael GruetJohn van Geest Cancer Research Centre, Nottingham Trent University, Nottingham NG11 8NS, UK.
Daniel CottonJohn van Geest Cancer Research Centre, Nottingham Trent University, Nottingham NG11 8NS, UK.
Clare CoveneyJohn van Geest Cancer Research Centre, Nottingham Trent University, Nottingham NG11 8NS, UK.
David J BoocockJohn van Geest Cancer Research Centre, Nottingham Trent University, Nottingham NG11 8NS, UK.ORCID 0000-0002-7333-3549
Sarah WagnerJohn van Geest Cancer Research Centre, Nottingham Trent University, Nottingham NG11 8NS, UK.
Lucie KomorowskiJohn van Geest Cancer Research Centre, Nottingham Trent University, Nottingham NG11 8NS, UK.
Robert C ReesJohn van Geest Cancer Research Centre, Nottingham Trent University, Nottingham NG11 8NS, UK.
A Graham PockleyJohn van Geest Cancer Research Centre, Nottingham Trent University, Nottingham NG11 8NS, UK.
A Christopher GarnerSchool of Science and Technology, Nottingham Trent University, Nottingham NG11 8NS, UK.
John D WallisSchool of Science and Technology, Nottingham Trent University, Nottingham NG11 8NS, UK.
Amanda K MilesJohn van Geest Cancer Research Centre, Nottingham Trent University, Nottingham NG11 8NS, UK.ORCID 0000-0002-5388-938X
Desmond G PoweJohn van Geest Cancer Research Centre, Nottingham Trent University, Nottingham NG11 8NS, UK.
Nottingham Trent University · GBNottingham University Hospitals NHS Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastasis is associated with poor prognosis in breast cancer. Although some studies suggest beta-blockers increase survival by delaying metastasis, others have been discordant. This study provides both insights into the anomalous findings and identifies potential biomarkers that may be treatment targets. Cell line models of basal-type and oestrogen receptor-positive breast cancer were profiled for basal levels of adrenoceptor gene/protein expression, and β2-adrenoceptor mediated cell behaviour including migration, invasion, adhesion, and survival in response to adrenoceptor agonist/antagonist treatment. Protein profiling and histology identified biomarkers and drug targets. Baseline levels of adrenoceptor gene expression are higher in basal-type rather than oestrogen receptor-positive cancer cells. Norepinephrine (NE) treatment increased invasive capacity in all cell lines but did not increase proliferation/survival. Protein profiling revealed the upregulation of the pro-metastatic gene Ly6/PLAUR Domain-Containing Protein 3 (LYPD3) in norepinephrine-treated MDA-MB-468 cells. Histology confirmed selective LYPD3 expression in primary and metastatic breast tumour samples. These findings demonstrate that basal-type cancer cells show a more aggressive adrenoceptor-β2-activated phenotype in the resting and stimulated state, which is attenuated by adrenoceptor-β2 inhibition. This study also highlights the first association between ADRβ2 signalling and LYPD3; its knockdown significantly reduced the basal and norepinephrine-induced activity of MCF-7 cells in vitro. The regulation of ADRβ2 signalling by LYPD3 and its metastasis promoting activities, reveal LYPD3 as a promising therapeutic target in the treatment of breast and other cancers.

Indexed as

beta-blockersbreast cancerLYPD3β2-adrenoceptor

Identifiers

PMID32098331
PMCPMC7168268
OpenAlexW3006733396

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.