Evidence map›Paper›PMID 26013699›Full record

ArticleScientific reports2015

Three-dimensional cage-like microscaffolds for cell invasion studies.

Barbara Spagnolo, Virgilio Brunetti, Godefroy Leménager, Elisa De Luca, Leonardo Sileo, Teresa Pellegrino, Pier Paolo Pompa, Massimo De Vittorio, Ferruccio Pisanello

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 60 citations in OpenAlex.

  1. Quantifying cell traction forces at the single-fiber scale in 3D: An approach based on deformable photopolymerized fiber arrays.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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

9 authors at 2 institutions in 1 country.

Barbara Spagnolo1] Center for Biomolecular Nanotechnologies, Istituto Italiano di Tecnologia, Via Barsanti, 73010 Arnesano (Lecce), Italy [2] Dipartimento di Ingegneria dell'Innovazione, Università del Salento, via per Monteroni, 73100 Lecce, Italy.
Virgilio BrunettiCenter for Biomolecular Nanotechnologies, Istituto Italiano di Tecnologia, Via Barsanti, 73010 Arnesano (Lecce), Italy.
Godefroy LeménagerCenter for Biomolecular Nanotechnologies, Istituto Italiano di Tecnologia, Via Barsanti, 73010 Arnesano (Lecce), Italy.
Elisa De LucaCenter for Biomolecular Nanotechnologies, Istituto Italiano di Tecnologia, Via Barsanti, 73010 Arnesano (Lecce), Italy.
Leonardo SileoCenter for Biomolecular Nanotechnologies, Istituto Italiano di Tecnologia, Via Barsanti, 73010 Arnesano (Lecce), Italy.
Teresa PellegrinoNanochemistry Department, Istituto Italiano di Tecnologia, via Morego 30, 16163 Genova, Italy.
Pier Paolo PompaCenter for Biomolecular Nanotechnologies, Istituto Italiano di Tecnologia, Via Barsanti, 73010 Arnesano (Lecce), Italy.
Massimo De Vittorio1] Center for Biomolecular Nanotechnologies, Istituto Italiano di Tecnologia, Via Barsanti, 73010 Arnesano (Lecce), Italy [2] Dipartimento di Ingegneria dell'Innovazione, Università del Salento, via per Monteroni, 73100 Lecce, Italy.
Ferruccio PisanelloCenter for Biomolecular Nanotechnologies, Istituto Italiano di Tecnologia, Via Barsanti, 73010 Arnesano (Lecce), Italy.
Italian Institute of Technology · ITCenter for Biomolecular Nanotechnologies · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer cell motility is one of the major events involved in metastatic process. Tumor cells that disseminate from a primary tumor can migrate into the vascular system and, being carried by the bloodstream, transmigrate across the endothelium, giving rise to a new tumor site. However, during the invasive process, tumor cells must pass through the extracellular matrix, whose structural and mechanical properties define the parameters of the migration process. Here, we propose 3D-complex cage-like microstructures, realized by two-photon (TP) direct laser writing (DLW), to analyze cell migration through pores significantly smaller than the cell nucleus. We found that the ability to traverse differently sized pores depends on the metastatic potential and on the invasiveness of the cell lines, allowing to establish a pore-area threshold value able to discriminate between non-tumorigenic and tumorigenic human breast cells.

Indexed as

Microscopy, ConfocalTime-Lapse ImagingCell Line, TumorCell MovementCoculture TechniquesHumansNonmuscle Myosin Type IIANonmuscle Myosin Type IIA

Identifiers

PMID26013699
PMCPMC4650598
OpenAlexW2264200897

What OpenQuestion holds

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LicenceCC BY
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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.