Evidence map›Paper›PMID 34491259›Full record

ArticleJournal of materials chemistry. B2021

Influence of surface topography on PCL electrospun scaffolds for liver tissue engineering.

Yunxi Gao, Anthony Callanan

Open access · hybridAbstract read
In one paragraph

Article in Journal of materials chemistry. B, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 17% of its field
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

12 citing papers in PubMed, 27 citations in OpenAlex.

  1. Multifunctional Electrospun PCL/Starch/n-AlInternational journal of molecular sciences · 2026
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  10. Frontiers in bioengineering and biotechnology · 2023
    Article
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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

2 authors at 1 institution in 1 country.

Yunxi GaoInstitute of Bioengineering, School of Engineering, The University of Edinburgh, Edinburgh, UK. Anthony.Callanan@ed.ac.uk.ORCID 0000-0001-6793-3954
Anthony CallananInstitute of Bioengineering, School of Engineering, The University of Edinburgh, Edinburgh, UK. Anthony.Callanan@ed.ac.uk.ORCID 0000-0002-1871-2853
University of Edinburgh · GB

Funding

Medical Research Council MR/K017047/1Medical Research Council MR/L012766/1Medical Research Council MR/L022974/1
6 · The paper itself

Abstract

Severe liver disease is one of the most common causes of death globally. Currently, whole organ transplantation is the only therapeutic method for end-stage liver disease treatment, however, the need for donor organs far outweighs demand. Recently liver tissue engineering is starting to show promise for alleviating part of this problem. Electrospinning is a well-known method to fabricate a nanofibre scaffold which mimics the natural extracellular matrix that can support cell growth. This study aims to investigate liver cell responses to topographical features on electrospun fibres. Scaffolds with large surface depression (2 μm) (LSD), small surface depression (0.37 μm) (SSD), and no surface depression (NSD) were fabricated by using a solvent-nonsolvent system. A liver cell line (HepG2) was seeded onto the scaffolds for up to 14 days. The SSD group exhibited higher levels of cell viability and DNA content compared to the other groups. Additionally, the scaffolds promoted gene expression of albumin, with all cases having similar levels, while the cell growth rate was altered. Furthermore, the scaffold with depressions showed 0.8 MPa higher ultimate tensile strength compared to the other groups. These results suggest that small depressions might be preferred by HepG2 cells over smooth and large depression fibres and highlight the potential for tailoring liver cell responses.

Indexed as

Tissue EngineeringBiocompatible MaterialsCell SurvivalCollagen Type I, alpha 1 ChainGene Expression RegulationHep G2 CellsHumansLiverPolyestersPorositySerum Albumin, HumanSurface PropertiesTensile StrengthTissue ScaffoldsBiocompatible MaterialsCollagen Type I, alpha 1 ChainpolycaprolactonePolyestersSerum Albumin, Human

Identifiers

PMID34491259
PMCPMC8493469
OpenAlexW3196319648

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.