Evidence map›Paper›PMID 25703025›Full record

ArticleCellular signalling2015

Activation of β2-adrenergic receptor by (R,R')-4'-methoxy-1-naphthylfenoterol inhibits proliferation and motility of melanoma cells.

Artur Wnorowski, Mariola Sadowska, Rajib K Paul, Nagendra S Singh, Anna Boguszewska-Czubara, Lucita Jimenez, Kotb Abdelmohsen, Lawrence Toll, Krzysztof Jozwiak, Michel Bernier and 1 more

Abstract read
In one paragraph

Article in Cellular signalling, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Novel fenoterol derivatives as suppressors of ERK1/2 phosphorylation in melanoma.Naunyn-Schmiedeberg's archives of pharmacology · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. The Role of β-Blockers in Melanoma.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2020
    Review
  10. Article
  11. Article
  12. Article
  13. To block it, or not to block it?Journal of cancer research and clinical oncology · 2017
    Article
  14. Article
  15. Concurrent activation of βCellular signalling · 2017
    Article
  16. Frontiers in pharmacology · 2017
    Article
  17. Article
  18. 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

11 authors at 4 institutions in 2 countries.

Artur WnorowskiDepartment of Chemistry, Medical University of Lublin, 20-093 Lublin, Poland; Laboratory of Clinical Investigation, National Institute on Aging, NIH, Baltimore, MD 21224, USA. Electronic address: artur.wnorowski@gmail.com.
Mariola SadowskaUniversity of Maryland Greenebaum Cancer Center, Baltimore, MD 21201, USA. Electronic address: mariolas349@gmail.com.
Rajib K PaulLaboratory of Clinical Investigation, National Institute on Aging, NIH, Baltimore, MD 21224, USA. Electronic address: rajibkpaul@gmail.com.
Nagendra S SinghLaboratory of Clinical Investigation, National Institute on Aging, NIH, Baltimore, MD 21224, USA. Electronic address: nagendra.singh@nih.gov.
Anna Boguszewska-CzubaraDepartment of Medicinal Chemistry, Medical University of Lublin, 20-093 Lublin, Poland. Electronic address: anna.boguszewska-czubara@am.lublin.pl.
Lucita JimenezSRI International, Menlo Park, CA 94025, USA. Electronic address: lucita.jimenez@sri.com.
Kotb AbdelmohsenLaboratory of Genetics, National Institute on Aging, NIH, Baltimore, MD 21224, USA. Electronic address: abdelmohsenk@grc.nia.nih.gov.
Lawrence TollTorrey Pines Institute for Molecular Studies, Port St. Lucie, FL 34987, USA. Electronic address: ltoll@tpims.org.
Krzysztof JozwiakDepartment of Chemistry, Medical University of Lublin, 20-093 Lublin, Poland. Electronic address: krzysztof.jozwiak@umlub.pl.
Michel BernierTranslational Gerontology Branch, National Institute on Aging, NIH, Baltimore, MD 21224, USA. Electronic address: Bernierm@mail.nih.gov.
Irving W WainerLaboratory of Clinical Investigation, National Institute on Aging, NIH, Baltimore, MD 21224, USA. Electronic address: iwwainer@mitchellwoods.com.
National Institute on Aging · USMedical University of Lublin · PLSRI International · USTorrey Pines Institute For Molecular Studies · US

Funding

Disease Status Drug Metabolism and New Drug Discovery ZIAAG000297 · NIA · NATIONAL INSTITUTE ON AGING · PI EGAN, JOSEPHINE · 2009 to 2025
$38.2M
Intramural NIH HHS ZIA AG000297NIA NIH HHS N01-AG-3-1009
6 · The paper itself

Abstract

(R,R')-4'-methoxy-1-naphthylfenoterol [(R,R')-MNF] is a highly-selective β2 adrenergic receptor (β2-AR) agonist. Incubation of a panel of human-derived melanoma cell lines with (R,R')-MNF resulted in a dose- and time-dependent inhibition of motility as assessed by in vitro wound healing and xCELLigence migration and invasion assays. Activity of (R,R')-MNF positively correlated with the β2-AR expression levels across tested cell lines. The anti-motility activity of (R,R')-MNF was inhibited by the β2-AR antagonist ICI-118,551 and the protein kinase A inhibitor H-89. The adenylyl cyclase activator forskolin and the phosphodiesterase 4 inhibitor Ro 20-1724 mimicked the ability of (R,R')-MNF to inhibit migration of melanoma cell lines in culture, highlighting the importance of cAMP for this phenomenon. (R,R')-MNF caused significant inhibition of cell growth in β2-AR-expressing cells as monitored by radiolabeled thymidine incorporation and xCELLigence system. The MEK/ERK cascade functions in cellular proliferation, and constitutive phosphorylation of MEK and ERK at their active sites was significantly reduced upon β2-AR activation with (R,R')-MNF. Protein synthesis was inhibited concomitantly both with increased eEF2 phosphorylation and lower expression of tumor cell regulators, EGF receptors, cyclin A and MMP-9. Taken together, these results identified β2-AR as a novel potential target for melanoma management, and (R,R')-MNF as an efficient trigger of anti-tumorigenic cAMP/PKA-dependent signaling in β2-AR-expressing lesions.

Indexed as

Adrenergic beta-2 Receptor AgonistsAntineoplastic AgentsCell Line, TumorCell MovementCell ProliferationCyclic AMPFenoterolHumansMelanomaReceptors, Adrenergic, beta-2Signal Transduction4'-methoxy-1-naphthylfenoterolAdrenergic beta-2 Receptor AgonistsAntineoplastic AgentsCyclic AMPFenoterolReceptors, Adrenergic, beta-2Beta2 adrenoreceptor selective agonistBeta blockerMelanocortin 1 receptorMelanocyteMetastasisMigration

Identifiers

PMID25703025
PMCPMC4361792
OpenAlexW1991374291

What OpenQuestion holds

Textmetadata
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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.