Evidence map›Paper›PMID 37175397›Full record

ArticleInternational journal of molecular sciences2023

Cyclic Stretch-Induced Mechanical Stress Applied at 1 Hz Frequency Can Alter the Metastatic Potential Properties of SAOS-2 Osteosarcoma Cells.

Giulia Alloisio, David Becerril Rodriguez, Marco Luce, Chiara Ciaccio, Stefano Marini, Antonio Cricenti, Magda Gioia

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

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  4. Review
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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

7 authors at 2 institutions in 1 country.

Giulia AlloisioDepartment of Clinical Sciences and Translational Medicine, University of Rome 'Tor Vergata', Via Montpellier 1, I-00133 Rome, Italy.
David Becerril RodriguezInstitute of Structure Matter del Consiglio Nazionale delle Ricerche ISM-CNR, Via del Fosso del Cavaliere 100, I-00133 Rome, Italy.
Marco LuceInstitute of Structure Matter del Consiglio Nazionale delle Ricerche ISM-CNR, Via del Fosso del Cavaliere 100, I-00133 Rome, Italy.
Chiara CiaccioDepartment of Clinical Sciences and Translational Medicine, University of Rome 'Tor Vergata', Via Montpellier 1, I-00133 Rome, Italy.ORCID 0000-0003-1119-2303
Stefano MariniDepartment of Clinical Sciences and Translational Medicine, University of Rome 'Tor Vergata', Via Montpellier 1, I-00133 Rome, Italy.
Antonio CricentiInstitute of Structure Matter del Consiglio Nazionale delle Ricerche ISM-CNR, Via del Fosso del Cavaliere 100, I-00133 Rome, Italy.ORCID 0000-0002-8581-3478
Magda GioiaDepartment of Clinical Sciences and Translational Medicine, University of Rome 'Tor Vergata', Via Montpellier 1, I-00133 Rome, Italy.ORCID 0000-0003-0352-3547
University of Rome Tor Vergata · ITInstitute of Structure of Matter · IT

Funding

Italian Ministery of University and Research Prin 2017SNRXH3Tor Vergata Univeristy of Rome E84120000620005
6 · The paper itself

Abstract

Recently, there has been an increasing focus on cellular morphology and mechanical behavior in order to gain a better understanding of the modulation of cell malignancy. This study used uniaxial-stretching technology to select a mechanical regimen able to elevate SAOS-2 cell migration, which is crucial in osteosarcoma cell pathology. Using confocal and atomic force microscopy, we demonstrated that a 24 h 0.5% cyclic elongation applied at 1 Hz induces morphological changes in cells. Following mechanical stimulation, the cell area enlarged, developing a more elongated shape, which disrupted the initial nuclear-to-cytoplasm ratio. The peripheral cell surface also increased its roughness. Cell-based biochemical assays and real-time PCR quantification showed that these morphologically induced changes are unrelated to the osteoblastic differentiative grade. Interestingly, two essential cell-motility properties in the modulation of the metastatic process changed following the 24 h 1 Hz mechanical stimulation. These were cell adhesion and cell migration, which, in fact, were dampened and enhanced, respectively. Notably, our results showed that the stretch-induced up-regulation of cell motility occurs through a mechanism that does not depend on matrix metalloproteinase (MMP) activity, while the inhibition of ion-stretch channels could counteract it. Overall, our results suggest that further research on mechanobiology could represent an alternative approach for the identification of novel molecular targets of osteosarcoma cell malignancy.

Indexed as

Bone NeoplasmsOsteosarcomaCell DifferentiationCell MovementHumansIon ChannelsStress, MechanicalIon Channelsbiomechanical responsecell migrationcell morphologycell structural deformationcyclic mechanical strainmalignant bone cellsmechanical stressmechanobiologymechano-sensingosteosarcoma

Identifiers

PMID37175397
PMCPMC10178551
OpenAlexW4366827090

What Socratic 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 Socratic graph.