Evidence map›Paper›PMID 31588689›Full record

ArticleCancer medicine2019

Beta-blockers exert potent anti-tumor effects in cutaneous and uveal melanoma.

Prisca Bustamante, Denise Miyamoto, Alicia Goyeneche, Paulina García de Alba Graue, Eva Jin, Thupten Tsering, Ana Beatriz Dias, Miguel N Burnier, Julia V Burnier

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.5field-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

28 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  9. Bioadhesive Eudragit RLPharmaceutics · 2025
    Article
  10. Review
  11. The βAdvances in pharmacological and pharmaceutical sciences · 2024
    Review
  12. Article
  13. Review
  14. Targeting the βThe Journal of pathology · 2023
    Article
  15. Article
  16. Drug repurposing-an emerging strategy in cancer therapeutics.Naunyn-Schmiedeberg's archives of pharmacology · 2022
    Review
  17. Review
  18. Article
  19. Review
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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

9 authors at 1 institution in 1 country.

Prisca BustamanteCancer Research Program, Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Denise MiyamotoCancer Research Program, Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Alicia GoyenecheCancer Research Program, Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Paulina García de Alba GraueCancer Research Program, Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Eva JinCancer Research Program, Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Thupten TseringCancer Research Program, Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Ana Beatriz DiasCancer Research Program, Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Miguel N BurnierCancer Research Program, Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Julia V BurnierCancer Research Program, Research Institute of the McGill University Health Centre, Montreal, QC, Canada.ORCID 0000-0002-2184-2157
McGill University Health Centre · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMelanoma is a life-threatening group of cancers mainly affecting the skin (cutaneous melanoma, CM) and the eyes (uveal melanoma, UM). Nearly half of patients with UM develop liver metastases regardless of the primary treatment. For this reason, adjuvant therapy to prevent disease progression is essential to improve survival of patients with melanoma. Beta-adrenoceptors (β-AR) have emerged as novel targets to inhibit tumor growth and dissemination in CM, but have not been investigated in UM.

methodsThe aim of this study was to comprehensively evaluate the effects of a non-selective β-blocker in UM and CM. Propranolol was tested on four UM and two CM cell lines to determine the effects of this beta-blocker. The expression of β-AR in UM was assessed in enucleated eyes of 36 patients.

resultsThe results showed that propranolol exerts potent anti-proliferative effects, attenuates migration, reduces VEGF and induces cell cycle arrest and apoptosis in both UM and CM in a dose-dependent manner. Furthermore, levels of cell-free DNA released from the cells correlated to propranolol treatment and may be an indicator of treatment response. Finally, immunohistochemical analysis revealed the expression of β1 and β2 adrenoceptors in all UM patients, with higher expression seen in the more aggressive epithelioid versus less aggressive spindle cells.

conclusionsCollectively our data suggest that a nonselective beta-blocker may be effective against melanoma. For the first time, we show potent anti-tumor effects in UM cells following propranolol administration and expression of β1 and β2 adrenoceptors in patient tissue.

Indexed as

Adrenergic beta-AntagonistsApoptosisCell Line, TumorCell MovementCell ProliferationDrug Screening Assays, AntitumorHumansMelanomaPrimary Cell CulturePropranololReceptors, Adrenergic, beta-1Receptors, Adrenergic, beta-2Skin NeoplasmsUveaUveal MelanomaUveal NeoplasmsADRB1 protein, humanADRB2 protein, humanAdrenergic beta-AntagonistsPropranololReceptors, Adrenergic, beta-1Receptors, Adrenergic, beta-2adjuvant therapybeta-blockersmelanomauveal melanoma

Identifiers

PMID31588689
PMCPMC6885887
OpenAlexW2979420081

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.