Evidence map›Paper›PMID 41140511›Full record

ArticleScience and technology of advanced materials2025

Exploring anti-cancer activities of epidermal growth factor-immobilized polymeric nanoparticles.

Shota Yamamoto, Chia-Jung Chang, Masao Kamimura, Jun Nakanishi

Abstract read
In one paragraph

Article in Science and technology of advanced materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Shota YamamotoResearch Center for Macromolecules & Biomaterials, National Institute for Materials Science (NIMS), Tsukuba, Ibaraki, Japan.ORCID https://orcid.org/0000-0002-7422-0968
Chia-Jung ChangResearch Center for Macromolecules & Biomaterials, National Institute for Materials Science (NIMS), Tsukuba, Ibaraki, Japan.
Masao KamimuraGraduate School of Advanced Engineering, Tokyo University of Science, Katsushika-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0001-8510-2935
Jun NakanishiResearch Center for Macromolecules & Biomaterials, National Institute for Materials Science (NIMS), Tsukuba, Ibaraki, Japan.ORCID https://orcid.org/0000-0003-4457-6581

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytotoxic agents targeting the epidermal growth factor receptor (EGFR) exhibit significant potential for cancer therapy as EGFR is overexpressed in various cancers. As alternatives to conventional EGFR inhibitors (EGFRi), which exert side effects on non-cancer cells, EGF-immobilized gold nanoparticles exhibit selective cytotoxicity in EGFR-overexpressing cancer cells by locally enhancing EGFR activation and modulating signal transduction through a signal condensation mechanism. However, considering real therapeutic applications, it is important to confirm that the same principle can be applied to polymeric nanoparticles, which are more suitable carriers owing to their biodegradability and biocompatibility, remains unclear. Therefore, in this study, we aimed to investigate the anti-cancer activities of EGF-conjugates with two kinds of polymeric nanoparticles: polystyrene nanoparticles and polymeric micelles. Initial mechanistic studies on phosphorylation signaling and cholesterol depletion revealed that EGF-polystyrene nanoparticles exhibited cytotoxicity against human cervical adenocarcinoma HeLa cells via local enhancement of EGFR activity in membrane rafts. Moreover, EGF-polymeric micelles exerted selective anti-cancer effects against EGFRi-resistant MDA-MB468 refractory triple-negative breast cancer cells after optimization of particle size. These results suggest that the unique anti-cancer effects of EGF nanoparticles are not dependent on the carrier platform. Furthermore, EGF nanoparticles exhibited high cytotoxicity against cancer cells responding poorly to conventional EGFR-targeted anti-cancer drugs, showing potential for future medical applications.

Indexed as

Anti-cancer drugsEGF-nanoparticle conjugatespolymeric micellestriple-negative breast cancer

Identifiers

PMID41140511
PMCPMC12551373

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.