Evidence map›Paper›PMID 36175895›Full record

ArticleJournal of nanobiotechnology2022

Enhanced natural killer cell anti-tumor activity with nanoparticles mediated ferroptosis and potential therapeutic application in prostate cancer.

Kwang-Soo Kim, Bongseo Choi, Hyunjun Choi, Min Jun Ko, Dong-Hwan Kim, Dong-Hyun Kim

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
8.7field-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

38 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
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  6. Effect of clinically relevant iron oxide nanoparticles on macrophage polarization, tumor growth and tumor microenvironment modulation.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Article
  7. Review
  8. Review
  9. Review
  10. Article
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  12. Inducing ferroptosis to improve cancer therapy: a promising tool for enhancing immunotherapy.Journal of experimental & clinical cancer research : CR · 2025
    Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Ferroptosis: CD8Cell death discovery · 2025
    Review
  20. Review
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

6 authors at 3 institutions in 2 countries.

Kwang-Soo KimDepartment of Radiology, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA.
Bongseo ChoiDepartment of Radiology, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA.
Hyunjun ChoiDepartment of Radiology, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA.
Min Jun KoDepartment of Radiology, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA.
Dong-Hwan KimSchool of Chemical Engineering, Sungkyunkwan University (SKKU), Suwon, 16419, Korea. dhkim1@skku.edu.
Dong-Hyun KimDepartment of Radiology, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA. dhkim@northwestern.edu.
Northwestern University · USUniversity of Illinois Chicago · USSungkyunkwan University · KR

Funding

Image-Guided Transcatheter Delivery of Natural Killer Cell Therapy Augmented with IFN-Gamma Eluting MicrospheresR01EB026207 · NIBIB · NORTHWESTERN UNIVERSITY AT CHICAGO · PI KIM, DONG-HYUN · 2018 to 2021
$1.4M
Ministry of Trade, Industry and Energy P0008746NIBIB NIH HHS R01 EB026207NIBIB NIH HHS R01EB026207
6 · The paper itself

Abstract

Ferroptosis provides an opportunity to overcome the cancer cell therapeutic resistance and modulate the immune system. Here an interaction between ferroptosis of cancer cells and natural killer (NK) cells was investigated with a clinical grade iron oxide nanoparticle (ferumoxytol) for potential synergistic anti-cancer effect of ferroptosis and NK cell therapy in prostate cancer. When ferumoxytol mediated ferroptosis of cancer cells was combined with NK cells, the NK cells' cytotoxic function was increased. Observed ferroptosis mediated NK cell activation was also confirmed with IFN-γ secretion and lytic degranulation. Upregulation of ULBPs, which is one of the ligands for NK cell activating receptor NKG2D, was observed in the co-treatment of ferumoxytol mediated ferroptosis and NK cells. Additionally, HMGB1 and PD-L1 expression of cancer cells were observed in the treatment of ferroptosis + NK cells. Finally, in vivo therapeutic efficacy of ferumoxytol mediated ferroptosis and NK cell therapy was observed with significant tumor volume regression in a prostate cancer mice model. These results suggest that the NK cells' function can be enhanced with ferumoxytol mediated ferroptosis.

Indexed as

FerroptosisHMGB1 ProteinNanoparticlesProstatic NeoplasmsAnimalsB7-H1 AntigenCell Line, TumorCytotoxicity, ImmunologicFerrosoferric OxideHumansKiller Cells, NaturalMaleMiceNK Cell Lectin-Like Receptor Subfamily KB7-H1 AntigenFerrosoferric OxideHMGB1 ProteinNK Cell Lectin-Like Receptor Subfamily KCancer therapyFerroptosisNanomedicineNK cellsProstate cancer

Identifiers

PMID36175895
PMCPMC9523925
OpenAlexW4297962997

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.