Evidence map›Paper›PMID 35957076›Full record

ArticleNanomaterials (Basel, Switzerland)2022

Anti-Fn14-Conjugated Prussian Blue Nanoparticles as a Targeted Photothermal Therapy Agent for Glioblastoma.

Nicole F Bonan, Debbie K Ledezma, Matthew A Tovar, Preethi B Balakrishnan, Rohan Fernandes

Open access · goldAbstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Fn14-Targeted Gold Nanorods for Augmenting Laser Thermal Therapy for High-Grade Gliomas.Langmuir : the ACS journal of surfaces and colloids · 2025
    Article
  2. Review
  3. Article
  4. Emerging nanoplatforms towards microenvironment-responsive glioma therapy.Medical oncology (Northwood, London, England) · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Nanomaterials for Drug Delivery and Cancer Therapy.Nanomaterials (Basel, Switzerland) · 2023
    Article
  11. 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

5 authors at 1 institution in 1 country.

Nicole F BonanGeorge Washington Cancer Center, George Washington University, Washington, DC 20052, USA.ORCID 0000-0001-9053-8362
Debbie K LedezmaGeorge Washington Cancer Center, George Washington University, Washington, DC 20052, USA.ORCID 0000-0001-7922-3773
Matthew A TovarGeorge Washington Cancer Center, George Washington University, Washington, DC 20052, USA.ORCID 0000-0002-2922-7642
Preethi B BalakrishnanGeorge Washington Cancer Center, George Washington University, Washington, DC 20052, USA.
Rohan FernandesGeorge Washington Cancer Center, George Washington University, Washington, DC 20052, USA.ORCID 0000-0001-9439-4626
George Washington University · US

Funding

Engineered Ensemble Nanoimmunotherapies for CancerR37CA226171 · NCI · GEORGE WASHINGTON UNIVERSITY · PI FERNANDES, ROHAN · 2019 to 2024
$2.6M
George Washington University Institutional FundsNCI NIH HHS R37 CA226171NCI NIH HHS R37CA226171
6 · The paper itself

Abstract

Prussian blue nanoparticles (PBNPs) are effective photothermal therapy (PTT) agents: they absorb near-infrared radiation and reemit it as heat via phonon-phonon relaxations that, in the presence of tumors, can induce thermal and immunogenic cell death. However, in the context of central nervous system (CNS) tumors, the off-target effects of PTT have the potential to result in injury to healthy CNS tissue. Motivated by this need for targeted PTT agents for CNS tumors, we present a PBNP formulation that targets fibroblast growth factor-inducible 14 (Fn14)-expressing glioblastoma cell lines. We conjugated an antibody targeting Fn14, a receptor abundantly expressed on many glioblastomas but near absent on healthy CNS tissue, to PBNPs (aFn14-PBNPs). We measured the attachment efficiency of aFn14 onto PBNPs, the size and stability of aFn14-PBNPs, and the ability of aFn14-PBNPs to induce thermal and immunogenic cell death and target and treat glioblastoma tumor cells in vitro. aFn14 remained stably conjugated to the PBNPs for at least 21 days. Further, PTT with aFn14-PBNPs induced thermal and immunogenic cell death in glioblastoma tumor cells. However, in a targeted treatment assay, PTT was only effective in killing glioblastoma tumor cells when using aFn14-PBNPs, not when using PBNPs alone. Our methodology is novel in its targeting moiety, tumor application, and combination with PTT. To the best of our knowledge, PBNPs have not been investigated as a targeted PTT agent in glioblastoma via conjugation to aFn14. Our results demonstrate a novel and effective method for delivering targeted PTT to aFn14-expressing tumor cells via aFn14 conjugation to PBNPs.

Indexed as

aFn14 antibodyglioblastomaimmunogenic cell deathphotothermal therapyprussian blue nanoparticlestargeted therapythermal therapy

Identifiers

PMID35957076
PMCPMC9370342
OpenAlexW4289341900

What Socratic 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 Socratic graph.