Evidence map›Paper›PMID 32985601›Full record

ArticleScientific reports2020

Ambrisentan, an endothelin receptor type A-selective antagonist, inhibits cancer cell migration, invasion, and metastasis.

Lucy Kappes, Ruba L Amer, Sabine Sommerlatte, Ghada Bashir, Corinna Plattfaut, Frank Gieseler, Timo Gemoll, Hauke Busch, Abeer Altahrawi, Ashraf Al-Sbiei and 16 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Pooled it
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  11. Repurposing of the Drug Tezosentan for Cancer Therapy.Current issues in molecular biology · 2023
    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

26 authors at 6 institutions in 6 countries.

Lucy Kappes *Department of Rheumatology and Clinical Immunology, University of Lübeck, Lübeck, Germany.
Ruba L Amer *Department of Medical Microbiology and Immunology, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.
Sabine SommerlatteDepartment of Rheumatology and Clinical Immunology, University of Lübeck, Lübeck, Germany.
Ghada BashirDepartment of Medical Microbiology and Immunology, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.
Corinna PlattfautSection Experimental Oncology, University Hospital and Medical School (UKSH), University of Lübeck, Lübeck, Germany.
Frank GieselerSection Experimental Oncology, University Hospital and Medical School (UKSH), University of Lübeck, Lübeck, Germany.ORCID http://orcid.org/0000-0001-6409-3822
Timo GemollSection for Translational Surgical Oncology and Biobanking, Department of Surgery, University of Lübeck and University Medical Center Schleswig-Holstein, Lübeck, Germany.
Hauke BuschLübeck Institute for Experimental Dermatology (LIED) and Institute of Cardiogenetics, University of Lübeck, Lübeck, Germany.ORCID http://orcid.org/0000-0003-4763-4521
Abeer AltahrawiDepartment of Pathology, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.
Ashraf Al-SbieiDepartment of Medical Microbiology and Immunology, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.
Shoja M HaneefaDepartment of Medical Microbiology and Immunology, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.
Kholoud ArafatDepartment of Pharmacology and Therapeutics, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.ORCID http://orcid.org/0000-0003-0549-7223
Lena F SchimkeDepartment of Rheumatology and Clinical Immunology, University of Lübeck, Lübeck, Germany.
Nadia El KhawankyDepartment of Hematology and Oncology, Faculty of Medicine, The University of Freiburg, Freiburg, Germany.
Kai Schulze-ForsterCellTrend GmbH, Luckenwalde, Brandenburg, Germany.
Harald HeideckeCellTrend GmbH, Luckenwalde, Brandenburg, Germany.
Anja Kerstein-StaehleDepartment of Rheumatology and Clinical Immunology, University of Lübeck, Lübeck, Germany.
Gabriele MarschnerDepartment of Rheumatology and Clinical Immunology, University of Lübeck, Lübeck, Germany.
Silke PitannDepartment of Rheumatology and Clinical Immunology, University of Lübeck, Lübeck, Germany.
Hans D OchsDepartment of Pediatrics, University of Washington School of Medicine, and Seattle Children's Research Institute, Seattle, WA, USA.
Antje MuellerDepartment of Rheumatology and Clinical Immunology, University of Lübeck, Lübeck, Germany.
Samir AttoubDepartment of Pharmacology and Therapeutics, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.
Maria J Fernandez-CabezudoDepartment of Biochemistry, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates.
Gabriela RiemekastenDepartment of Rheumatology and Clinical Immunology, University of Lübeck, Lübeck, Germany.
Basel K Al-Ramadi *Department of Medical Microbiology and Immunology, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, United Arab Emirates. ramadi.b@uaeu.ac.ae.
Otavio Cabral-Marques *Department of Immunology, Institute of Biomedical Sciences, University of São Paulo, Lineu Prestes Avenue, 1730, São Paulo, SP, Brazil. otavio.cmarques@gmail.com.
University of Lübeck · DEUnited Arab Emirates University · AEInstitute of Pathology Celle · DESeattle Children's Hospital · USUniversidade de São Paulo · BRUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several studies reported a central role of the endothelin type A receptor (ETAR) in tumor progression leading to the formation of metastasis. Here, we investigated the in vitro and in vivo anti-tumor effects of the FDA-approved ETAR antagonist, Ambrisentan, which is currently used to treat patients with pulmonary arterial hypertension. In vitro, Ambrisentan inhibited both spontaneous and induced migration/invasion capacity of different tumor cells (COLO-357 metastatic pancreatic adenocarcinoma, OvCar3 ovarian carcinoma, MDA-MB-231 breast adenocarcinoma, and HL-60 promyelocytic leukemia). Whole transcriptome analysis using RNAseq indicated Ambrisentan's inhibitory effects on the whole transcriptome of resting and PAR2-activated COLO-357 cells, which tended to normalize to an unstimulated profile. Finally, in a pre-clinical murine model of metastatic breast cancer, treatment with Ambrisentan was effective in decreasing metastasis into the lungs and liver. Importantly, this was associated with a significant enhancement in animal survival. Taken together, our work suggests a new therapeutic application for Ambrisentan in the treatment of cancer metastasis.

Indexed as

Cell MovementAnimalsAntihypertensive AgentsApoptosisBreast NeoplasmsCell ProliferationEndothelin A Receptor AntagonistsFemaleHumansLiver NeoplasmsLung NeoplasmsMiceMice, Inbred BALB CMice, NudeNeoplasm InvasivenessPhenylpropionatesambrisentanAntihypertensive AgentsEndothelin A Receptor AntagonistsPhenylpropionatesPyridazines

Identifiers

PMID32985601
PMCPMC7522204
OpenAlexW3088137181

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.