Evidence map›Paper›PMID 23275323›Full record

ArticleCroatian medical journal2012

Morphological alterations of T24 cells on flat and nanotubular TiO2 surfaces.

Roghayeh Imani, Doron Kabaso, Mateja Erdani Kreft, Ekaterina Gongadze, Samo Penic, Kristina Elersic, Andrej Kos, Peter Veranic, Robert Zorec, Ales Iglic

Abstract read
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Article in Croatian medical journal, 2012. 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

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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.

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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

10 authors.

Roghayeh ImaniFaculty of Electrical Engineering, University of Ljubljana, Ljubljana, Slovenia.
Doron Kabaso
Mateja Erdani Kreft
Ekaterina Gongadze
Samo Penic
Kristina Elersic
Andrej Kos
Peter Veranic
Robert Zorec
Ales Iglic

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate morphological alterations of malignant cancer cells (T24) of urothelial origin seeded on flat titanium (Ti) and nanotubular TiO(2) (titanium dioxide) nanostructures.

methodsUsing anodization method, TiO(2) surfaces composed of vertically aligned nanotubes of 50-100 nm diameters were produced. The flat Ti surface was used as a reference. The alteration in the morphology of cancer cells was evaluated using scanning electron microscopy (SEM). A computational model, based on the theory of membrane elasticity, was constructed to shed light on the biophysical mechanisms responsible for the observed changes in the contact area of adhesion.

resultsLarge diameter TiO(2) nanotubes exhibited a significantly smaller contact area of adhesion (P<0.0001) and had more membrane protrusions (eg, microvilli and intercellular membrane nanotubes) than on flat Ti surface. Numerical membrane dynamics simulations revealed that the low adhesion energy per unit area would hinder the cell spreading on the large diameter TiO(2) nanotubular surface, thus explaining the small contact area.

conclusionThe reduction in the cell contact area in the case of large diameter TiO(2) nanotube surface, which does not enable formation of the large enough number of the focal adhesion points, prevents spreading of urothelial cells.

Indexed as

Tissue ScaffoldsBiocompatible MaterialsCell AdhesionHumansMicroscopy, Electron, ScanningNanotubesSurface PropertiesTitaniumTumor Cells, CulturedUrologic NeoplasmsBiocompatible MaterialsTitaniumtitanium dioxide

Identifiers

PMID23275323
PMCPMC3541584

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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.