Iron accumulation in tumor-associated macrophages marks an improved overall survival in patients with lung adenocarcinoma.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
05 08 2019
Historique:
received: 13 11 2018
accepted: 08 07 2019
entrez: 7 8 2019
pubmed: 7 8 2019
medline: 24 10 2020
Statut: epublish

Résumé

Iron-loaded tumor-associated macrophages (iTAMs) show a pro-inflammatory phenotype, hallmarked by anti-tumorigenic activity and an ability to attenuate tumor growth. Here we explored the relevance of these findings in lung cancer patients by investigating the impact of the iTAM content in the tumor microenvironment (TME) on patient survival. We analyzed 102 human non-small cell lung cancer (NSCLC) paraffin-embedded archival tissue samples for iron levels and macrophage numbers. Interestingly, patients with lung adenocarcinoma accumulating iron in the TME show higher numbers of M1-like pro-inflammatory TAMs and a survival advantage compared to iron-negative patients. By contrast, in patients with lung squamous cell carcinoma iron in the TME does not affect survival, suggesting a unique influence of iron on different histological subtypes of non-small cell lung cancer (NSCLC). We conclude that in lung adenocarcinoma iron may serve as a prognostic marker for patient survival and as a potential therapeutic target for anti-cancer therapy.

Identifiants

pubmed: 31383898
doi: 10.1038/s41598-019-47833-x
pii: 10.1038/s41598-019-47833-x
pmc: PMC6683135
doi:

Substances chimiques

Iron E1UOL152H7

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

11326

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Auteurs

Carl Maximilian Thielmann (CM)

Department of Pediatric Oncology, Hematology and Immunology, University of Heidelberg, Heidelberg, Germany.
Molecular Medicine Partnership Unit (MMPU), University of Heidelberg & EMBL, Heidelberg, Germany.
Translational Lung Research Center (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.

Milene Costa da Silva (M)

Department of Pediatric Oncology, Hematology and Immunology, University of Heidelberg, Heidelberg, Germany.
Molecular Medicine Partnership Unit (MMPU), University of Heidelberg & EMBL, Heidelberg, Germany.
Graduate Program in Areas of Basic and Applied Biology (GABBA), University of Porto, Porto, Portugal.
German Cancer Research Center (DKFZ), University of Heidelberg, Heidelberg, Germany.
Translational Lung Research Center (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.

Thomas Muley (T)

Translational Research Unit, Thoraxklinik, at University Hospital Heidelberg, Heidelberg, Germany.
Translational Lung Research Center (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.

Michael Meister (M)

Translational Research Unit, Thoraxklinik, at University Hospital Heidelberg, Heidelberg, Germany.
Translational Lung Research Center (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany.

Esther Herpel (E)

Institute of Pathology, University of Heidelberg, Heidelberg, Germany.
Tissue Bank of the National Center for Tumor Diseases (NCT), Heidelberg, Germany.

Martina U Muckenthaler (MU)

Department of Pediatric Oncology, Hematology and Immunology, University of Heidelberg, Heidelberg, Germany. martina.muckenthaler@med.uni-heidelberg.de.
Molecular Medicine Partnership Unit (MMPU), University of Heidelberg & EMBL, Heidelberg, Germany. martina.muckenthaler@med.uni-heidelberg.de.
Translational Lung Research Center (TLRC), German Center for Lung Research (DZL), Heidelberg, Germany. martina.muckenthaler@med.uni-heidelberg.de.

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Classifications MeSH