Evidence map›Paper›PMID 42255629›Full record

ArticleACS omega2026

Mucoadhesive Nanoemulsion Enhances the Antineoplastic Potential of Naringenin in Bladder Cancer Cell Lines.

Kamila de Fátima da Anunciação, Tatiane Roquete Amparo, Lucas Resende Dutra Sousa, Viviane Flores Xavier, Paula Melo de Abreu Vieira, Orlando David Henrique Dos Santos, Geraldo Célio Brandão, Glenda Nicioli da Silva

Abstract read
In one paragraph

Article in ACS omega, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Kamila de Fátima da AnunciaçãoPostgraduate Program on Biological Sciences, Institute of Biological Sciences, Federal University of Ouro Preto, 35400-000 Ouro Preto, Brazil.
Tatiane Roquete AmparoPostgraduate Program on Pharmaceutical Sciences, Federal University of Ouro Preto, 35400-000 Ouro Preto, Brazil.
Lucas Resende Dutra SousaPostgraduate Program on Pharmaceutical Sciences, Federal University of Ouro Preto, 35400-000 Ouro Preto, Brazil.
Viviane Flores XavierPostgraduate Program on Pharmaceutical Sciences, Federal University of Ouro Preto, 35400-000 Ouro Preto, Brazil.
Paula Melo de Abreu VieiraPostgraduate Program on Biological Sciences, Institute of Biological Sciences, Federal University of Ouro Preto, 35400-000 Ouro Preto, Brazil.ORCID https://orcid.org/0000-0001-7033-7686
Orlando David Henrique Dos SantosPostgraduate Program on Pharmaceutical Sciences, Federal University of Ouro Preto, 35400-000 Ouro Preto, Brazil.ORCID https://orcid.org/0000-0002-8904-6990
Geraldo Célio BrandãoPostgraduate Program on Pharmaceutical Sciences, Federal University of Ouro Preto, 35400-000 Ouro Preto, Brazil.
Glenda Nicioli da SilvaPostgraduate Program on Biological Sciences, Institute of Biological Sciences, Federal University of Ouro Preto, 35400-000 Ouro Preto, Brazil.ORCID https://orcid.org/0000-0001-9751-3379

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Naringenin exhibits anticancer properties against various types of cancer. Bladder cancer is among the most prevalent cancers worldwide and is characterized by a high recurrence rate because of resistance to standard chemotherapy. Nanotechnology represents a prospective approach to counteracting the challenges associated with the therapeutic application of naringenin in the treatment of bladder cancer. The aim of this study was to evaluate the antineoplastic activity of naringenin in high-grade bladder cancer cell lines (J82 and UM-UC-3) and to develop nanoemulsions. The assessment of cellular toxicity was conducted using the sulforhodamine B method, clonogenic survival using crystal violet staining, cell migration by the wound healing assay, changes in the cell cycle using flow cytometry, and expression of the specific long noncoding RNAs

Identifiers

PMID42255629
PMCPMC13234646

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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.