Evidence map›Paper›PMID 41692043›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2026

Effect of clinically relevant iron oxide nanoparticles on macrophage polarization, tumor growth and tumor microenvironment modulation.

Karolin Roemhild, Yanchen Li, Roman A Barmin, Seyed Mohammadali Dadfar, Ekaterina Savina, Kim Lindelauf, Diana Moeckel, Elena Rama, Teresa Lemainque, Finn von Maltzahn and 12 more

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

22 authors.

Karolin RoemhildInstitute of Experimental Molecular Imaging, University Hospital RWTH Aachen, Aachen, Germany; Institute of Pathology, University Hospital RWTH Aachen, Aachen, Germany.
Yanchen LiInstitute of Experimental Molecular Imaging, University Hospital RWTH Aachen, Aachen, Germany.
Roman A BarminInstitute of Experimental Molecular Imaging, University Hospital RWTH Aachen, Aachen, Germany.
Seyed Mohammadali DadfarInstitute of Experimental Molecular Imaging, University Hospital RWTH Aachen, Aachen, Germany; Ardena Oss, Kloosterstraat 9, 5349 AB Oss, the Netherlands.
Ekaterina SavinaInstitute of Experimental Molecular Imaging, University Hospital RWTH Aachen, Aachen, Germany.
Kim LindelaufInstitute of Experimental Molecular Imaging, University Hospital RWTH Aachen, Aachen, Germany.
Diana MoeckelInstitute of Experimental Molecular Imaging, University Hospital RWTH Aachen, Aachen, Germany.
Elena RamaInstitute of Experimental Molecular Imaging, University Hospital RWTH Aachen, Aachen, Germany.
Teresa LemainqueInstitute of Experimental Molecular Imaging, University Hospital RWTH Aachen, Aachen, Germany; Department of Diagnostic and Interventional Radiology, Medical Faculty, University Hospital RWTH Aachen, Aachen, Germany.
Finn von MaltzahnInstitute of Experimental Molecular Imaging, University Hospital RWTH Aachen, Aachen, Germany.
Sven Thoröe-BovelethInstitute of Occupational, Social and Environmental Medicine, University Hospital RWTH Aachen, Aachen, Germany.
Robert PolaInstitute of Macromolecular Chemistry, Czech Academy of Sciences, Prague, Czech Republic.
Tomas EtrychInstitute of Macromolecular Chemistry, Czech Academy of Sciences, Prague, Czech Republic.
Ruth Knuechel-ClarkeInstitute of Pathology, University Hospital RWTH Aachen, Aachen, Germany.
Peter BoorInstitute of Pathology, University Hospital RWTH Aachen, Aachen, Germany; Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf (CIO ABCD), Aachen, Germany.
Thomas KrausInstitute of Occupational, Social and Environmental Medicine, University Hospital RWTH Aachen, Aachen, Germany.
Volkmar SchulzInstitute for Imaging and Computer Vision, University Hospital RWTH Aachen, Aachen, Germany.
Jan GrimmDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Fabian KiesslingInstitute of Experimental Molecular Imaging, University Hospital RWTH Aachen, Aachen, Germany.
Saskia von StillfriedInstitute of Pathology, University Hospital RWTH Aachen, Aachen, Germany; Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf (CIO ABCD), Aachen, Germany.
Roger M PallaresInstitute of Experimental Molecular Imaging, University Hospital RWTH Aachen, Aachen, Germany. Electronic address: rmoltopallar@ukaachen.de.
Twan LammersInstitute of Experimental Molecular Imaging, University Hospital RWTH Aachen, Aachen, Germany; Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf (CIO ABCD), Aachen, Germany. Electronic address: tlammers@ukaachen.de.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Exploring PSMA Biology in Tumor neovasculatureR01CA212379 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI GRIMM, JAN · 2017 to 2021
$3.5M
Smart and self-reporting clinical nano carriers for drug deliveryR01CA215700 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI GRIMM, JAN · 2017 to 2021
$3.5M
Exploiting ferroportin for cancer imaging and therapyR01CA218615 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI GRIMM, JAN · 2017 to 2021
$2.7M
Multicolor PET to interrogate cancer biologyR01EB033000 · NIBIB · SLOAN-KETTERING INST CAN RESEARCH · PI Jan Grimm, Vladimir Ponomarev · 2023 to 2026
$2.6M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA212379NCI NIH HHS R01 CA215700NCI NIH HHS R01 CA218615NIBIB NIH HHS R01 EB033000
6 · The paper itself

Abstract

Macrophages are key regulators of the tumor microenvironment (TME) and attractive targets for nanomedicine therapies. Because intracellular iron can promote pro-inflammatory macrophage polarization, superparamagnetic iron oxide nanoparticles (SPION) have been proposed as potential antitumor therapeutics. Nevertheless, their ability to remodel the TME and inhibit tumor growth has remained unclear. Here, we evaluated whether the commercially available SPION formulations Feraheme and Synomag can regulate macrophage polarization, modulate the microenvironment, affect tumor growth, and alter tumor-targeted drug delivery. In vitro, despite being internalized by macrophages highly efficiently, Feraheme and Synomag only elicited modest effects on macrophage polarization markers. In vivo, repeated intravenous administrations of Feraheme in an orthotopic and syngeneic 4 T1 triple-negative breast cancer model resulted in significant increases in intratumoral iron levels. However, they did not affect tumor growth nor statistically significant altered tumor-associated macrophage density and polarization, T-cell subsets, or the composition of the TME. Accordingly, pre-treatment with Feraheme did not alter tumor vascularization or collagen content, nor did it result in a statistically significant improvement in the delivery of a model polymeric nanocarrier. Together, these results support the use of SPION as tracers for macrophage-targeted imaging applications rather than as antitumor therapeutics and TME priming agents.

Indexed as

DextransMacrophagesMagnetic Iron Oxide NanoparticlesTriple Negative Breast NeoplasmsTumor MicroenvironmentAnimalsCell Line, TumorFemaleHumansDextransIron metabolismIron oxide nanoparticlesMacrophage polarizationMagnetic resonance imagingSPIONTumor microenvironment

Identifiers

PMID41692043
PMCPMC13450206

What OpenQuestion holds

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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.