Evidence map›Paper›PMID 33489885›Full record

ReviewFrontiers in oncology2020

Targeting Adrenomedullin in Oncology: A Feasible Strategy With Potential as Much More Than an Alternative Anti-Angiogenic Therapy.

Ramiro Vázquez, Maria E Riveiro, Caroline Berenguer-Daizé, Anthony O'Kane, Julie Gormley, Olivier Touzelet, Keyvan Rezai, Mohamed Bekradda, L'Houcine Ouafik

Open access · goldAbstract readReview
In one paragraph

Review 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 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  4. Adrenomedullin in Tumorigenesis and Cancer Progression.International journal of molecular sciences · 2025
    Review
  5. Current and novel biomarkers in cardiogenic shock.European journal of heart failure · 2025
    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 4 institutions in 2 countries.

Ramiro VázquezPreclinical Department, Early Drug Development Group (E2DG), Boulogne-Billancourt, France.
Maria E RiveiroPreclinical Department, Early Drug Development Group (E2DG), Boulogne-Billancourt, France.
Caroline Berenguer-DaizéAix Marseille University, CNRS, INP, Institute of NeuroPhysiopathology, Marseille, France.
Anthony O'KaneDiscovery and Scientific Affairs Department, Fusion Antibodies plc., Belfast, United Kingdom.
Julie GormleyDiscovery and Scientific Affairs Department, Fusion Antibodies plc., Belfast, United Kingdom.
Olivier TouzeletDiscovery and Scientific Affairs Department, Fusion Antibodies plc., Belfast, United Kingdom.
Keyvan RezaiDepartment of Radio-Pharmacology, Institute Curie-René Huguenin Hospital, Saint-Cloud, France.
Mohamed BekraddaPreclinical Department, Early Drug Development Group (E2DG), Boulogne-Billancourt, France.
L'Houcine OuafikAix Marseille University, CNRS, INP, Institute of NeuroPhysiopathology, Marseille, France.
Centre National de la Recherche Scientifique · FRInstitut Curie · FRInstitut de Neurophysiopathologie · FRItalian Institute of Technology · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development, maintenance and metastasis of solid tumors are highly dependent on the formation of blood and lymphatic vessels from pre-existing ones through a series of processes that are respectively known as angiogenesis and lymphangiogenesis. Both are mediated by specific growth-stimulating molecules, such as the vascular endothelial growth factor (VEGF) and adrenomedullin (AM), secreted by diverse cell types which involve not only the cancerogenic ones, but also those constituting the tumor stroma (i.e., macrophages, pericytes, fibroblasts, and endothelial cells). In this sense, anti-angiogenic therapy represents a clinically-validated strategy in oncology. Current therapeutic approaches are mainly based on VEGF-targeting agents, which, unfortunately, are usually limited by toxicity and/or tumor-acquired resistance. AM is a ubiquitous peptide hormone mainly secreted in the endothelium with an important involvement in blood vessel development and cardiovascular homeostasis. In this review, we will introduce the state-of-the-art in terms of AM physiology, while putting a special focus on its pro-tumorigenic role, and discuss its potential as a therapeutic target in oncology. A large amount of research has evidenced AM overexpression in a vast majority of solid tumors and a correlation between AM levels and disease stage, progression and/or vascular density has been observed. The analysis presented here indicates that the involvement of AM in the pathogenesis of cancer arises from: 1) direct promotion of cell proliferation and survival; 2) increased vascularization and the subsequent supply of nutrients and oxygen to the tumor; 3) and/or alteration of the cell phenotype into a more aggressive one. Furthermore, we have performed a deep scrutiny of the pathophysiological prominence of each of the AM receptors (AM

Indexed as

adrenomedullinAM1 and AM2angiogenesiscancermetastasisRAMP1-3

Identifiers

PMID33489885
PMCPMC7815935
OpenAlexW3118484999

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Registered trials

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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.