Evidence map›Paper›PMID 32819314›Full record

ArticleBMC cancer2020

Breast cancer mammospheres secrete Adrenomedullin to induce lipolysis and browning of adjacent adipocytes.

Martin Paré, Cédric Y Darini, Xi Yao, Bérengère Chignon-Sicard, Samah Rekima, Simon Lachambre, Virginie Virolle, Adriana Aguilar-Mahecha, Mark Basik, Christian Dani and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 44 citations in OpenAlex.

  1. TheInternational journal of molecular sciences · 2021
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  12. Adrenomedullin in Tumorigenesis and Cancer Progression.International journal of molecular sciences · 2025
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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

11 authors at 3 institutions in 2 countries.

Martin ParéUniversité Côte d'Azur, CNRS, INSERM, iBV, Nice, France.
Cédric Y DariniSegal Cancer Center, Lady Davis Institute for Medical Research, Sir Mortimer B. Davis Jewish General Hospital, McGill University, Montréal, Québec, Canada.
Xi YaoUniversité Côte d'Azur, CNRS, INSERM, iBV, Nice, France.
Bérengère Chignon-SicardUniversité Côte d'Azur, Pasteur 2 Hospital, Department of Plastic and Reconstructive Surgery, Nice, France.
Samah RekimaUniversité Côte d'Azur, CNRS, INSERM, iBV, Nice, France.
Simon LachambreUniversité Côte d'Azur, CNRS, INSERM, iBV, Nice, France.
Virginie VirolleUniversité Côte d'Azur, CNRS, INSERM, iBV, Nice, France.
Adriana Aguilar-MahechaSegal Cancer Center, Lady Davis Institute for Medical Research, Sir Mortimer B. Davis Jewish General Hospital, McGill University, Montréal, Québec, Canada.
Mark BasikSegal Cancer Center, Lady Davis Institute for Medical Research, Sir Mortimer B. Davis Jewish General Hospital, McGill University, Montréal, Québec, Canada.
Christian DaniUniversité Côte d'Azur, CNRS, INSERM, iBV, Nice, France.
Annie LadouxUniversité Côte d'Azur, CNRS, INSERM, iBV, Nice, France. ladoux@unice.fr.ORCID http://orcid.org/0000-0003-3857-2621
Centre National de la Recherche Scientifique · FRJewish General Hospital · CAUniversité Côte d'Azur · FR

Funding

Agence Nationale de la Recherche #ANR-11-LABX-0028-01Agence Nationale de la Recherche #ANR-18-CE18-006 (hiPS-adipospheres)Association pour la Recherche sur le Cancer 2016 1204713
6 · The paper itself

Abstract

backgroundCancer cells cooperate with cells that compose their environment to promote tumor growth and invasion. Among them, adipocytes provide lipids used as a source of energy by cancer cells and adipokines that contribute to tumor expansion. Mechanisms supporting the dynamic interactions between cancer cells and stromal adipocytes, however, remain unclear.

methodsWe set-up a co-culture model with breast cancer cells grown in 3D as mammospheres and human adipocytes to accurately recapitulate intrinsic features of tumors, such as hypoxia and cancer cell-adipocytes interactions.

resultsHerein, we observed that the lipid droplets' size was reduced in adipocytes adjacent to the mammospheres, mimicking adipocyte morphology on histological sections. We showed that the uncoupling protein UCP1 was expressed in adipocytes close to tumor cells on breast cancer histological sections as well as in adipocytes in contact with the mammospheres. Mammospheres produced adrenomedullin (ADM), a multifactorial hypoxia-inducible peptide while ADM receptors were detected in adipocytes. Stimulation of adipocytes with ADM promoted UCP1 expression and increased HSL phosphorylation, which activated lipolysis. Invalidation of ADM in breast cancer cells dramatically reduced UCP1 expression in adipocytes.

conclusionsBreast tumor cells secreted ADM that modified cancer-associated adipocytes through paracrine signaling, leading to metabolic changes and delipidation. Hence, ADM appears to be crucial in controlling the interactions between cancer cells and adipocytes and represents an excellent target to hinder them.

Indexed as

Paracrine CommunicationAdipocytesAdrenomedullinBreastBreast NeoplasmsCell HypoxiaCoculture TechniquesFemaleHumansLipid DropletsLipolysisMCF-7 CellsSpheroids, CellularTumor MicroenvironmentUncoupling Protein 1ADM protein, humanAdrenomedullinUCP1 protein, humanUncoupling Protein 1AdipocytesAdrenomedullinBreast cancerBrowningLipolysisUCP1

Identifiers

PMID32819314
PMCPMC7441622
OpenAlexW3066725994

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.