Evidence map›Paper›PMID 25390644›Full record

ArticlePloS one2014

Investigation of adhesion and mechanical properties of human glioma cells by single cell force spectroscopy and atomic force microscopy.

Laura Andolfi, Eugenia Bourkoula, Elisa Migliorini, Anita Palma, Anja Pucer, Miran Skrap, Giacinto Scoles, Antonio Paolo Beltrami, Daniela Cesselli, Marco Lazzarino

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

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  9. Imaging the subcellular viscoelastic properties of mouse oocytes.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  16. Biomedical optics express · 2020
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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.

Laura AndolfiIstituto Officina dei Materiali-National Research Council, Trieste, Italy.
Eugenia BourkoulaDepartment of Medical and Biological Sciences, University of Udine, Udine, Italy.
Elisa MiglioriniDépartement de Chimie Moléculaire, Ingénierie et Interactions Bio Moléculaires, Université Joseph Fourier, Grenoble, France.
Anita PalmaDepartment of Medical and Biological Sciences, University of Udine, Udine, Italy.
Anja PucerDepartment of Medical and Biological Sciences, University of Udine, Udine, Italy.
Miran SkrapDepartment of Medical and Biological Sciences, University of Udine, Udine, Italy.
Giacinto ScolesDepartment of Medical and Biological Sciences, University of Udine, Udine, Italy.
Antonio Paolo BeltramiDepartment of Medical and Biological Sciences, University of Udine, Udine, Italy.
Daniela CesselliDepartment of Medical and Biological Sciences, University of Udine, Udine, Italy.
Marco LazzarinoIstituto Officina dei Materiali-National Research Council, Trieste, Italy; Cluster in Biomedicine, Trieste, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Active cell migration and invasion is a peculiar feature of glioma that makes this tumor able to rapidly infiltrate into the surrounding brain tissue. In our recent work, we identified a novel class of glioma-associated-stem cells (defined as GASC for high-grade glioma--HG--and Gasc for low-grade glioma--LG) that, although not tumorigenic, act supporting the biological aggressiveness of glioma-initiating stem cells (defined as GSC for HG and Gsc for LG) favoring also their motility. Migrating cancer cells undergo considerable molecular and cellular changes by remodeling their cytoskeleton and cell interactions with surrounding environment. To get a better understanding about the role of the glioma-associated-stem cells in tumor progression, cell deformability and interactions between glioma-initiating stem cells and glioma-associated-stem cells were investigated. Adhesion of HG/LG-cancer cells on HG/LG-glioma-associated stem cells was studied by time-lapse microscopy, while cell deformability and cell-cell adhesion strengths were quantified by indentation measurements by atomic force microscopy and single cell force spectroscopy. Our results demonstrate that for both HG and LG glioma, cancer-initiating-stem cells are softer than glioma-associated-stem cells, in agreement with their neoplastic features. The adhesion strength of GSC on GASC appears to be significantly lower than that observed for Gsc on Gasc. Whereas, GSC spread and firmly adhere on Gasc with an adhesion strength increased as compared to that obtained on GASC. These findings highlight that the grade of glioma-associated-stem cells plays an important role in modulating cancer cell adhesion, which could affect glioma cell migration, invasion and thus cancer aggressiveness. Moreover this work provides evidence about the importance of investigating cell adhesion and elasticity for new developments in disease diagnostics and therapeutics.

Indexed as

Brain NeoplasmsCell AdhesionCell MovementGliomaHumansMicroscopy, Atomic ForceNeoplasm InvasivenessNeoplastic Stem CellsSpectrum AnalysisTumor Cells, Cultured

Identifiers

PMID25390644
PMCPMC4229222

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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.