Evidence map›Paper›PMID 40148366›Full record

ArticleScientific reports2025

Exploring the effects of paclitaxel-loaded zein nanoparticles on human ovarian carcinoma cells.

Stefania Scicchitano, Agnese Gagliardi, Nicola Ambrosio, Eleonora Vecchio, Cinzia Garofalo, Anna Martina Battaglia, Francesco Saverio Costanzo, Maria Concetta Faniello, Donato Cosco

Abstract read
In one paragraph

Article in Scientific reports, 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. Review
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

9 authors.

Stefania Scicchitano *Laboratory of Biochemistry and Cellular Biology, Department of Experimental and Clinical Medicine, University of Catanzaro Magna Græcia, 88100, Catanzaro, Italy.
Agnese Gagliardi *Department of Health Sciences, University of Catanzaro Magna Græcia, 88100, Catanzaro, Italy.
Nicola AmbrosioDepartment of Health Sciences, University of Catanzaro Magna Græcia, 88100, Catanzaro, Italy.
Eleonora VecchioLaboratory of Biochemistry and Cellular Biology, Department of Experimental and Clinical Medicine, University of Catanzaro Magna Græcia, 88100, Catanzaro, Italy.
Cinzia GarofaloLaboratory of Biochemistry and Cellular Biology, Department of Experimental and Clinical Medicine, University of Catanzaro Magna Græcia, 88100, Catanzaro, Italy.
Anna Martina BattagliaLaboratory of Biochemistry and Cellular Biology, Department of Experimental and Clinical Medicine, University of Catanzaro Magna Græcia, 88100, Catanzaro, Italy.
Francesco Saverio CostanzoLaboratory of Biochemistry and Cellular Biology, Department of Experimental and Clinical Medicine, University of Catanzaro Magna Græcia, 88100, Catanzaro, Italy.
Maria Concetta Faniello *Laboratory of Biochemistry and Cellular Biology, Department of Experimental and Clinical Medicine, University of Catanzaro Magna Græcia, 88100, Catanzaro, Italy. faniello@unicz.it.
Donato Cosco *Department of Health Sciences, University of Catanzaro Magna Græcia, 88100, Catanzaro, Italy. donatocosco@unicz.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of innovative antitumor formulations that are able to increase the mortality of cancer cells while decreasing the efficacious pharmacological dosage is a fundamental goal of modern oncological research. In this study a paclitaxel (PTX)-nanomedicine was tested on two lines of human high-grade serous ovarian carcinoma (hHGS-OC). Zein, a vegetal protein, was employed to obtain nanoparticles containing the lipophilic compound (NanoPTX) characterized by a mean diameter of 160 nm, a narrow size distribution, a negative zeta potential and a prolonged release of the drug over time. NanoPTX was tested on HEY and COV362 cells demonstrating an increase of apoptosis, particularly on the papillary cystadenocarcinoma cells (55.2% p value 0.037 for NanoPTX vs 70.25%, p value 0.08 for PTX) with respect to the free form of the drug. The fluorescent nanosystems were characterized by a significant cell uptake after a few hours of incubation and they promoted a reduction in the intracellular reactive oxygen species. The results need to be validated on different hHGS-OC cells and the real efficacy of the proposed nanomedicine needs to be investigated using in vivo models of ovarian carcinoma.

Indexed as

Antineoplastic Agents, PhytogenicNanoparticlesOvarian NeoplasmsPaclitaxelZeinApoptosisCell Line, TumorCell SurvivalDrug CarriersFemaleHumansReactive Oxygen SpeciesAntineoplastic Agents, PhytogenicDrug CarriersPaclitaxelReactive Oxygen SpeciesZeinHigh grade serous ovarian carcinomaNanomedicineNanoparticlesPaclitaxelZein

Identifiers

PMID40148366
PMCPMC11950396

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Registered trials

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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.