Evidence map›Paper›PMID 28937680›Full record

ArticleNature chemistry2017

Salinomycin kills cancer stem cells by sequestering iron in lysosomes.

Trang Thi Mai, Ahmed Hamaï, Antje Hienzsch, Tatiana Cañeque, Sebastian Müller, Julien Wicinski, Olivier Cabaud, Christine Leroy, Amandine David, Verónica Acevedo and 7 more

Abstract read
In one paragraph

Article in Nature chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 304 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
304citing papers in PubMed, 1 pooled it
36.4field-weighted citation impact, top 1% 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

304 citing papers in PubMed, 1 synthesis or guideline pooled it, 602 citations in OpenAlex.

  1. Pooled it
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  8. An iron logic unites bacterial and cancer persister cells.Nature reviews. Molecular cell biology · 2026
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244 more citing papers are in PubMed but not listed here.

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 4 institutions in 3 countries.

Trang Thi MaiInstitut Curie, PSL Research University, Chemical Cell Biology Group, 26 rue d'Ulm, 75248 Paris Cedex 05, France.
Ahmed HamaïInstitut Necker-Enfants Malades, INSERM U1151-CNRS UMR8253, Université Paris Descartes-Sorbonne Paris Cité, 14 rue Maria Helena Vieira Da Silva, 75993 Paris Cedex 14, France.
Antje HienzschInstitut de Chimie des Substances Naturelles, UPR2301, 1 Avenue de la Terrasse, 91198 Gif-sur-Yvette Cedex, France.ORCID 0000-0003-0566-3658
Tatiana CañequeInstitut Curie, PSL Research University, Chemical Cell Biology Group, 26 rue d'Ulm, 75248 Paris Cedex 05, France.
Sebastian MüllerInstitut Curie, PSL Research University, Chemical Cell Biology Group, 26 rue d'Ulm, 75248 Paris Cedex 05, France.
Julien WicinskiAix Marseille Université, CNRS, INSERM, Institut Paoli-Calmettes, CRCM, Equipe Oncologie Moléculaire labellisée 'Ligue contre le cancer', 13009 Marseille, France.
Olivier CabaudAix Marseille Université, CNRS, INSERM, Institut Paoli-Calmettes, CRCM, Equipe Oncologie Moléculaire labellisée 'Ligue contre le cancer', 13009 Marseille, France.
Christine LeroyInstitut Necker-Enfants Malades, INSERM U1151-CNRS UMR8253, Université Paris Descartes-Sorbonne Paris Cité, 14 rue Maria Helena Vieira Da Silva, 75993 Paris Cedex 14, France.
Amandine DavidInstitut Necker-Enfants Malades, INSERM U1151-CNRS UMR8253, Université Paris Descartes-Sorbonne Paris Cité, 14 rue Maria Helena Vieira Da Silva, 75993 Paris Cedex 14, France.
Verónica AcevedoInstitut Curie, PSL Research University, Chemical Cell Biology Group, 26 rue d'Ulm, 75248 Paris Cedex 05, France.
Akihide RyoDepartment of Microbiology, Yokohama City University School of Medicine, Yokohama 236-0004, Japan.
Christophe GinestierAix Marseille Université, CNRS, INSERM, Institut Paoli-Calmettes, CRCM, Equipe Oncologie Moléculaire labellisée 'Ligue contre le cancer', 13009 Marseille, France.
Daniel BirnbaumAix Marseille Université, CNRS, INSERM, Institut Paoli-Calmettes, CRCM, Equipe Oncologie Moléculaire labellisée 'Ligue contre le cancer', 13009 Marseille, France.
Emmanuelle Charafe-JauffretAix Marseille Université, CNRS, INSERM, Institut Paoli-Calmettes, CRCM, Equipe Oncologie Moléculaire labellisée 'Ligue contre le cancer', 13009 Marseille, France.
Patrice CodognoInstitut Necker-Enfants Malades, INSERM U1151-CNRS UMR8253, Université Paris Descartes-Sorbonne Paris Cité, 14 rue Maria Helena Vieira Da Silva, 75993 Paris Cedex 14, France.
Maryam MehrpourInstitut Necker-Enfants Malades, INSERM U1151-CNRS UMR8253, Université Paris Descartes-Sorbonne Paris Cité, 14 rue Maria Helena Vieira Da Silva, 75993 Paris Cedex 14, France.
Raphaël RodriguezInstitut Curie, PSL Research University, Chemical Cell Biology Group, 26 rue d'Ulm, 75248 Paris Cedex 05, France.ORCID 0000-0001-7668-446X
Centre National de la Recherche Scientifique · FRDélégation Paris 5 · FRInstitut de Chimie des Substances Naturelles · FRYokohama City University · JP

Funding

European Research Council 647973
6 · The paper itself

Abstract

Cancer stem cells (CSCs) represent a subset of cells within tumours that exhibit self-renewal properties and the capacity to seed tumours. CSCs are typically refractory to conventional treatments and have been associated to metastasis and relapse. Salinomycin operates as a selective agent against CSCs through mechanisms that remain elusive. Here, we provide evidence that a synthetic derivative of salinomycin, which we named ironomycin (AM5), exhibits a more potent and selective activity against breast CSCs in vitro and in vivo, by accumulating and sequestering iron in lysosomes. In response to the ensuing cytoplasmic depletion of iron, cells triggered the degradation of ferritin in lysosomes, leading to further iron loading in this organelle. Iron-mediated production of reactive oxygen species promoted lysosomal membrane permeabilization, activating a cell death pathway consistent with ferroptosis. These findings reveal the prevalence of iron homeostasis in breast CSCs, pointing towards iron and iron-mediated processes as potential targets against these cells.

Indexed as

Antineoplastic AgentsBreast NeoplasmsCell ProliferationCell SurvivalDrug Screening Assays, AntitumorFemaleHomeostasisHumansIronLysosomesMolecular ConformationNeoplastic Stem CellsPolyether PolyketidesPyransReactive Oxygen SpeciesAntineoplastic AgentsIronPolyether PolyketidesPyransReactive Oxygen Speciessalinomycin

Identifiers

PMID28937680
PMCPMC5890907
OpenAlexW2614441145

What OpenQuestion holds

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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.