Evidence map›Paper›PMID 37954478›Full record

ArticleFrontiers in nanotechnology2023

Epidermal growth factor alters silica nanoparticle uptake and improves gold-nanoparticle-mediated gene silencing in A549 cells.

Eva Susnik, Amelie Bazzoni, Patricia Taladriz-Blanco, Sandor Balog, Aura Maria Moreno-Echeverri, Christina Glaubitz, Beatriz Brito Oliveira, Daniela Ferreira, Pedro Viana Baptista, Alke Petri-Fink and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in nanotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Organelle-Targeting Nanoparticles.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  3. Review
  4. 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

11 authors at 4 institutions in 2 countries.

Eva SusnikAdolphe Merkle Institute, University of Fribourg, Fribourg, Switzerland.
Amelie BazzoniAdolphe Merkle Institute, University of Fribourg, Fribourg, Switzerland.
Patricia Taladriz-BlancoInternational Iberian Nanotechnology Laboratory, Braga, Portugal.
Sandor BalogAdolphe Merkle Institute, University of Fribourg, Fribourg, Switzerland.
Aura Maria Moreno-EcheverriAdolphe Merkle Institute, University of Fribourg, Fribourg, Switzerland.
Christina GlaubitzAdolphe Merkle Institute, University of Fribourg, Fribourg, Switzerland.
Beatriz Brito Oliveirai4HB, UCIBIO, Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, Caparica, Portugal.
Daniela Ferreirai4HB, UCIBIO, Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, Caparica, Portugal.
Pedro Viana Baptistai4HB, UCIBIO, Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, Caparica, Portugal.
Alke Petri-FinkAdolphe Merkle Institute, University of Fribourg, Fribourg, Switzerland.
Barbara Rothen-RutishauserAdolphe Merkle Institute, University of Fribourg, Fribourg, Switzerland.
Adolphe Merkle Institute · CHUniversidade Nova de Lisboa · PTUniversity of Fribourg · CHInternational Iberian Nanotechnology Laboratory · PT

Funding

Swiss National Science Foundation 182881
6 · The paper itself

Abstract

Introduction: Delivery of therapeutic nanoparticles (NPs) to cancer cells represents a promising approach for biomedical applications. A key challenge for nanotechnology translation from the bench to the bedside is the low amount of administered NPs dose that effectively enters target cells. To improve NPs delivery, several studies proposed NPs conjugation with ligands, which specifically deliver NPs to target cells via receptor binding. One such example is epidermal growth factor (EGF), a peptide involved in cell signaling pathways that control cell division by binding to epidermal growth factor receptor (EGFR). However, very few studies assessed the influence of EGF present in the cell environment, on the cellular uptake of NPs. Methods: We tested if the stimulation of EGFR-expressing lung carcinomacells A549 with EGF affects the uptake of 59 nm and 422 nm silica (SiO Results: Our findings show that EGF binding to its receptor results in receptor autophosphorylation and initiate signaling pathways, leading to enhanced endocytosis of 59 nm SiO Discussion: These findings contribute to a better understanding of NPs uptake in the presence of EGF and that is a promising approach for improved NPs delivery.

Indexed as

endocytosisepidermal growth factorgene silencinggoldmolecular mechanismsnanomedicinenanoparticlessilica

Identifiers

PMID37954478
PMCPMC7615298
OpenAlexW4384500367

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.