Evidence map›Paper›PMID 40761526›Full record

ArticleBioImpacts : BI2025

Enhanced efficacy of breast cancer treatment with etoposide-graphene oxide nanogels: A novel nanomedicine approach.

Abbas Asoudeh-Fard, Milad Mohkam, Asghar Parsaei, Shadi Asghari, Antonio Lauto, Fatemeh Khoshnoudi, Mustafa Mhmood Salman Al-Mamoori, Mohadeseh Asoudeh-Fard, Hossine Ghasemi Sadabadi, Ahmad Gholami

Abstract read
In one paragraph

Article in BioImpacts : BI, 2025. 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
–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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  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

10 authors.

Abbas Asoudeh-FardInstitute Galilée-University Sorbonne, University Sorbonne Paris North, Paris, France.ORCID https://orcid.org/0000-0002-6552-5268
Milad MohkamAllergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Asghar ParsaeiNiko Gene Saba Company, Rayan Novin Pajoohan Pars, Biotechnology Company, Biotechnology Incubator, Shiraz University of Medicine Sciences, Shiraz, Iran.ORCID https://orcid.org/0000-0001-7852-8129
Shadi AsghariDepartment of Microbiology, Shiraz Branch Islamic Azad University, Shiraz, Iran.ORCID https://orcid.org/0009-0000-8978-8452
Antonio LautoSchool of Science, University of Western Sydney, Campbelltown, NSW, 2560, Australia.
Fatemeh KhoshnoudiDepartment of Cellular and Molecular, Zarghan Branch Islamic Azad University, Zarghan, Iran.ORCID https://orcid.org/0009-0000-6975-1708
Mustafa Mhmood Salman Al-MamooriDepartment of Cellular and Molecular, Mashhad Branch Islamic Azad University, Mashhad, Iran.ORCID https://orcid.org/0009-0000-9984-4972
Mohadeseh Asoudeh-FardDepartment of General Medicine, Azad Zahedan Medicine University, Zahedan, Iran.
Hossine Ghasemi SadabadiHematology and Oncology Research Center, Tabriz University of Medical Sciences Tabriz, Iran.
Ahmad GholamiBiotechnology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID https://orcid.org/0000-0003-1851-159X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Breast cancer represents a significant global health challenge, underscoring the need for innovative therapeutic strategies. This study explores the therapeutic potential of etoposide (ETO)-loaded graphene oxide (GO) nanogels to enhance the efficacy of breast cancer treatments. Methods: ETO-GO nanogels were synthesized and characterized using field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), and Fourier-transform infrared spectroscopy (FT-IR). Cytotoxicity was evaluated through MTT assays on MCF-7 breast cancer cells and normal HUVEC cells. Apoptosis induction was assessed using DAPI staining, flow cytometry, and quantitative reverse transcription polymerase chain reaction (qRT-PCR) to analyze changes in gene expression. Results: Characterization confirmed the formation of uniform, spherical nanogels with high ETO encapsulation efficiency. EDS and FT-IR analyses validated the successful loading of the drug onto the GO matrix. Cytotoxicity assays revealed a dose-dependent response, with significantly stronger effects observed in MCF-7 cells (20% viability at 100 µg/mL) than HUVEC cells (40% viability at the same concentration), indicating selective cytotoxicity. Apoptosis was verified through DAPI staining, which showed characteristics of nuclear fragmentation, and flow cytometry, identifying 15.35% of the treated cells as apoptotic. qRT-PCR analysis demonstrated an upregulation of pro-apoptotic genes (CASP3, CASP8, CASP9, BAX, PTEN) by as much as 8.3-fold, alongside a marked downregulation of the anti-apoptotic gene Bcl-2, confirming the potent induction of apoptosis by the nanogels. Conclusion: ETO-GO nanogels show promising potential for targeted breast cancer therapy, providing enhanced drug delivery and selective cytotoxicity. These findings warrant further in vivo studies to validate their clinical applicability.

Indexed as

Breast cancerChitosanEtoposideGraphene oxideMCF-7Nanogels

Identifiers

PMID40761526
PMCPMC12319212

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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.