Evidence map›Paper›PMID 30696910›Full record

ArticleScientific reports2019

Imaging endogenous macrophage iron deposits reveals a metabolic biomarker of polarized tumor macrophage infiltration and response to CSF1R breast cancer immunotherapy.

Avigdor Leftin, Nir Ben-Chetrit, Johanna A Joyce, Jason A Koutcher

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Macrophage Plasticity in Cancer Therapy: Function, Timing, and Tradeoffs.International journal of molecular sciences · 2026
    Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Iron and Cancer.Advances in experimental medicine and biology · 2025
    Review
  7. Review
  8. Review
  9. Targeting iron to contrast cancer progression.Current opinion in chemical biology · 2023
    Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. A novel roadmap connecting theEuropean radiology experimental · 2021
    Review
  17. Review
  18. Iron and Cancer: 2020 Vision.Cancer research · 2020
    Review
  19. Review
  20. Article
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

4 authors at 1 institution in 2 countries.

Avigdor LeftinDepartment of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA. leftina@mskcc.org.
Nir Ben-ChetritCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Johanna A JoyceCancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.ORCID 0000-0002-6332-2598
Jason A KoutcherDepartment of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Tumor Hypoxia Imaging - Laboratory and Clinical StudiesP01CA115675 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI ZANZONICO, PAT B · 2006 to 2010
$9.5M
Innate Metabolic MRI of Macrophage Infiltration in Prostate CancerF32CA206277 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI LEFTIN, AVIGDOR · 2016 to 2017
$127k
NCI NIH HHS F32 CA206277NCI NIH HHS P01 CA115675NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Iron deposits are a phenotypic trait of tumor-associated macrophages (TAMs). Histological iron imaging and contrast-agent free magnetic resonance imaging (MRI) can detect these deposits, but their presence  in human cancer, and correlation with immunotherapeutic response is largely untested. Here, primarily using these iron imaging approaches, we evaluated the spatial distribution of polarized macrophage populations containing high endogenous levels of iron in preclinical murine models and human breast cancer, and used them as metabolic biomarkers to correlate TAM infiltration with response to immunotherapy in preclinical trials. Macrophage-targeted inhibition of the colony stimulating factor 1 receptor (CSF1R) by immunotherapy was confirmed to inhibit macrophage accumulation and slow mammary tumor growth in mouse models while also reducing hemosiderin iron-laden TAM accumulation as measured by both iron histology and in vivo iron MRI (FeMRI). Spatial profiling of TAM iron deposit infiltration defined regions of maximal accumulation and response to the CSF1R inhibitor, and revealed differences between microenvironments of human cancer according to levels of polarized macrophage iron accumulation in stromal margins. We therefore demonstrate that iron deposition serves as an endogenous metabolic imaging biomarker of TAM infiltration in breast cancer that has high translational potential for evaluation of immunotherapeutic response.

Indexed as

AnimalsAntineoplastic AgentsBiomarkers, PharmacologicalBreast NeoplasmsCell DifferentiationCell MovementCells, CulturedDiagnostic ImagingFemaleHemosiderinHumansImmunotherapyIntracellular SpaceIronMacrophagesMiceAntineoplastic AgentsBiomarkers, PharmacologicalCSF1R protein, humanHemosiderinIronReceptor, Macrophage Colony-Stimulating FactorReceptors, Granulocyte-Macrophage Colony-Stimulating Factor

Identifiers

PMID30696910
PMCPMC6351660
OpenAlexW2914805964

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.