Evidence map›Paper›PMID 40594674›Full record

ArticleScientific reports2025

Screening of electrospun PS/PCL scaffolds for three-dimensional triple negative breast cancer cell culture: impact of solvent, hydrophobicity, and setup orientation.

Sira Ausellé-Bosch, Marta Pardo, Marta Pareja, Emma Polonio-Alcalá, Teresa Puig

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Biomimetic Scaffold-Based 3D Models for Decoding Cancer Biology and Advancing Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  2. Article
  3. Cancer cell dynamics on silica fibers.Scientific reports · 2025
    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

5 authors.

Sira Ausellé-BoschNew Therapeutic Targets Laboratory (TargetsLab) - Oncology Unit, Medical Sciences Department, University of Girona, Girona, Spain.
Marta PardoNew Therapeutic Targets Laboratory (TargetsLab) - Oncology Unit, Medical Sciences Department, University of Girona, Girona, Spain.
Marta ParejaNew Therapeutic Targets Laboratory (TargetsLab) - Oncology Unit, Medical Sciences Department, University of Girona, Girona, Spain.
Emma Polonio-AlcaláPrecision Oncology Group (OncoGIR-Pro), Girona BiomedicaI Research Institute (IDIBGI-CERCA), Girona, Spain.
Teresa PuigNew Therapeutic Targets Laboratory (TargetsLab) - Oncology Unit, Medical Sciences Department, University of Girona, Girona, Spain. teresa.puig@udg.edu.

Funding

Agencia Estatal de Investigación (Spain) and European Union NextGenerationEU PLEC2021-007523/AEI/10.13039/501100011033Fundación Ramón Areces, Instituto de Salud Carlos III and co-funded by European Union (ERDF/ESF, "A way to make Europe"/"Investing in your future") PI19/00372
6 · The paper itself

Abstract

Triple-Negative Breast Cancer (TNBC) presents a significant challenge due to its aggressiveness and lack of targeted therapies. Understanding the interaction between TNBC cells and the extracellular matrix (ECM) in three-dimensional (3D) culture systems is vital for developing accurate in vitro models. This study explores the impact of electrospinning setup orientation, solvent selection, and polymer composition on scaffold design and TNBC cell culture. Various polystyrene (PS) and poly-ε-caprolactone (PCL) combinations were electrospun using different solvent combinations (dichloromethane/dimethylformamide (DCM/DMF), tetrahydrofuran/dimethylformamide (THF/DMF), chloroform/dichloromethane (Chl/DCM) and acetone) and setup orientations (vertical, horizontal). Scaffolds were characterized using Scanning Electron Microscopy (SEM) to assess fiber diameter and pore size. Cell proliferation and morphology were analyzed through MTT assay, SEM and Confocal Laser Scanning Microscopy (CLSM). Pore area and fiber diameter were influenced by solvent combination (THF/DMF < DCM/DMF < acetone < Chl/DCM) and orientation setup (horizontal < vertical). Sterilization assay revealed that 1-hour immersion in 70% ethanol followed by 30 min ultra-violet (UV) light exposure achieved sterilization with minimal scaffold degradation. High proliferation with no significant reduction compared to monolayer culture was found in some scaffolds and variability in cell morphology between scaffolds was also detected. Results highlight the critical role of scaffold printing parameters for 3D TNBC cell culture. Electrospun PS/PCL 40/60 scaffolds dissolved in DCM/DMF are promising in vitro models, providing a valuable tool for cancer research.

Indexed as

Cell Culture Techniques, Three DimensionalPolyestersPolystyrenesSolventsTissue ScaffoldsTriple Negative Breast NeoplasmsCell Line, TumorCell ProliferationFemaleHumansHydrophobic and Hydrophilic InteractionsTissue EngineeringpolycaprolactonePolyestersPolystyrenesSolventsElectrospinningFiber morphologyPolystyrenePoly-ε-caprolactoneScaffoldsThree-dimensional cell culture

Identifiers

PMID40594674
PMCPMC12219171

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.