Evidence map›Paper›PMID 27788481›Full record

ArticleOncotarget2016

Propranolol induces a favourable shift of anti-tumor immunity in a murine spontaneous model of melanoma.

Ludovic Jean Wrobel, Lloyd Bod, Renée Lengagne, Masashi Kato, Armelle Prévost-Blondel, Frédérique-Anne Le Gal

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 2 pooled it
4.9field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 2 syntheses or guidelines pooled it, 78 citations in OpenAlex.

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  14. The neural addiction of cancer.Nature reviews. Cancer · 2023
    Review
  15. Radiation Therapy Exacerbates Tumor-Promoting Innervation and Nerve Signaling in Rectal Cancer.International journal of radiation oncology, biology, physics · 2023
    Article
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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

6 authors at 4 institutions in 3 countries.

Ludovic Jean WrobelHôpitaux Universitaires de Genève, Service de Dermatologie, Genève, Switzerland.
Lloyd BodInserm, U1016, Institut Cochin, Paris, France.
Renée LengagneInserm, U1016, Institut Cochin, Paris, France.
Masashi KatoDepartment of Occupational and Environmental Health, Nagoya University Graduate School of Medicine, Aichi, Japan.
Armelle Prévost-BlondelInserm, U1016, Institut Cochin, Paris, France.
Frédérique-Anne Le GalHôpitaux Universitaires de Genève, Service de Dermatologie, Genève, Switzerland.
Centre National de la Recherche Scientifique · FRHôpital Beau-Séjour · CHInstitut Cochin · FRNagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In a previous study on a xenograft model of melanoma, we showed that the beta-adrenergic receptor antagonist propranolol inhibits melanoma development by modulating angiogenesis, proliferation and cell survival. Stress hormones can influence tumor development in different ways and norepinephrine was shown to downregulate antitumor immune responses by favoring the accumulation of immunosuppressive cells, impairing the function of lymphocytes. We assessed the effect of propranolol on antitumor immune response in the MT/Ret mouse model of melanoma. Propranolol treatment delayed primary tumor growth and metastases development in MT/Ret mice. Consistent with our previous observations in human melanoma xenografts, propranolol induces a decrease in cell proliferation and vessel density in the primary tumors and in metastases. In this immunocompetent model, propranolol significantly reduced the infiltration of myeloid cells, particularly neutrophils, in the primary tumor. Inversely, cytotoxic tumor infiltrating lymphocytes were more frequent in the tumor stroma of treated mice. In a consistent manner, we observed the same shift in the proportions of infiltrating leukocytes in the metastases of treated mice. Our results suggest that propranolol, by decreasing the infiltration of immunosuppressive myeloid cells in the tumor microenvironment, restores a better control of the tumor by cytotoxic cells.

Indexed as

AnimalsAntineoplastic AgentsCell ProliferationLymphocytes, Tumor-InfiltratingMelanoma, ExperimentalMiceMice, Inbred C57BLNeoplasm MetastasisPropranololProto-Oncogene Proteins c-retSkin NeoplasmsTreatment OutcomeAntineoplastic AgentsPropranololProto-Oncogene Proteins c-retRet protein, mouseanti-tumor immunitybeta-blockermelanomanorepinephrinepropranolol

Identifiers

PMID27788481
PMCPMC5363624
OpenAlexW2535549547

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.