Evidence map›Paper›PMID 33489901›Full record

ArticleFrontiers in oncology2020

Targeting the Endothelin-1 Receptors Curtails Tumor Growth and Angiogenesis in Multiple Myeloma.

Anna Russignan, Giada Dal Collo, Anna Bagnato, Nicola Tamassia, Mattia Bugatti, Mirella Belleri, Luisa Lorenzi, Enrica Borsi, Riccardo Bazzoni, Michele Gottardi and 7 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

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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

17 authors at 5 institutions in 1 country.

Anna RussignanSection of Hematology and Bone-Marrow Transplant Unit, Department of Medicine, University of Verona, Verona, Italy.
Giada Dal ColloSection of Hematology and Bone-Marrow Transplant Unit, Department of Medicine, University of Verona, Verona, Italy.
Anna BagnatoPreclinical Models and New Therapeutic Agents Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Nicola TamassiaSection of General Pathology, Department of Medicine, University of Verona, Verona, Italy.
Mattia BugattiSection of Pathology, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Mirella BelleriExperimental Oncology and Immunology Unit, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Luisa LorenziSection of Pathology, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Enrica BorsiDepartment of Experimental Diagnostic and Specialty Medicine (DIMES), "L. and A. Seràgnoli", Bologna University, Bologna, Italy.
Riccardo BazzoniSection of Hematology and Bone-Marrow Transplant Unit, Department of Medicine, University of Verona, Verona, Italy.
Michele GottardiHematology Section, Ospedale Cà Foncello, Treviso, Italy.
Carolina TerragnaDepartment of Experimental Diagnostic and Specialty Medicine (DIMES), "L. and A. Seràgnoli", Bologna University, Bologna, Italy.
William VermiSection of Pathology, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Arianna GiacominiExperimental Oncology and Immunology Unit, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Marco PrestaExperimental Oncology and Immunology Unit, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Marco Antonio CassatellaSection of General Pathology, Department of Medicine, University of Verona, Verona, Italy.
Mauro KramperaSection of Hematology and Bone-Marrow Transplant Unit, Department of Medicine, University of Verona, Verona, Italy.
Cristina TecchioSection of Hematology and Bone-Marrow Transplant Unit, Department of Medicine, University of Verona, Verona, Italy.
University of Verona · ITUniversity of Brescia · ITUniversity of Bologna · ITCa' Foncello Hospital · ITIstituti di Ricovero e Cura a Carattere Scientifico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The endothelin-1 (ET-1) receptors were recently found to mediate pro-survival functions in multiple myeloma (MM) cells in response to autocrine ET-1. This study investigated the effectiveness of macitentan, a dual ET-1 receptor antagonist, in MM treatment, and the mechanisms underlying its activities. Macitentan affected significantly MM cell (RPMI-8226, U266, KMS-12-PE) survival and pro-angiogenic cytokine release by down-modulating ET-1-activated MAPK/ERK and HIF-1α pathways, respectively. HIF-1α silencing abrogated the ET-1 mediated induction of genes encoding for pro-angiogenic cytokines such as VEGF-A, IL-8, Adrenomedullin, and ET-1 itself. Upon exposure to macitentan, MM cells cultured in the presence of the hypoxia-mimetic agent CoCl

Indexed as

angiogenesisendothelin-1 axisHIF-1αmacitentanmultiple myeloma

Identifiers

PMID33489901
PMCPMC7820698
OpenAlexW3120330915

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.