Evidence map›Paper›PMID 37239904›Full record

ArticleInternational journal of molecular sciences2023

Shedding Light on Osteosarcoma Cell Differentiation: Impact on Biomineralization and Mitochondria Morphology.

Francesca Rossi, Giovanna Picone, Concettina Cappadone, Andrea Sorrentino, Marta Columbaro, Giovanna Farruggia, Emilio Catelli, Giorgia Sciutto, Silvia Prati, Robert Oliete and 4 more

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 11% 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, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
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

14 authors at 4 institutions in 2 countries.

Francesca RossiDepartment of Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.
Giovanna PiconeDepartment of Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.ORCID 0000-0003-4174-4164
Concettina CappadoneDepartment of Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.ORCID 0000-0002-3874-6815
Andrea SorrentinoMistral Beamline, ALBA Synchrotron Light Source, Cerdanyola del Valles, 08290 Barcelona, Spain.ORCID 0000-0002-3235-8950
Marta ColumbaroPiattaforma di Microscopia Elettronica, IRCCS Istituto Ortopedico Rizzoli, 40136 Bologna, Italy.ORCID 0000-0002-4439-8976
Giovanna FarruggiaDepartment of Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.ORCID 0000-0003-3599-7034
Emilio CatelliDepartment of Chemistry "G. Ciamician", Università di Bologna, Ravenna Campus, Via Guaccimanni, 42, 48121 Ravenna, Italy.
Giorgia SciuttoDepartment of Chemistry "G. Ciamician", Università di Bologna, Ravenna Campus, Via Guaccimanni, 42, 48121 Ravenna, Italy.
Silvia PratiDepartment of Chemistry "G. Ciamician", Università di Bologna, Ravenna Campus, Via Guaccimanni, 42, 48121 Ravenna, Italy.
Robert OlieteMistral Beamline, ALBA Synchrotron Light Source, Cerdanyola del Valles, 08290 Barcelona, Spain.
Alice PasiniDepartment of Electrical, Electronic and Information Engineering "Guglielmo Marconi" (DEI), University of Bologna, Via dell'Università 50, 47522 Cesena, Italy.
Eva PereiroMistral Beamline, ALBA Synchrotron Light Source, Cerdanyola del Valles, 08290 Barcelona, Spain.ORCID 0000-0001-7626-5935
Stefano IottiDepartment of Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.ORCID 0000-0003-1426-6400
Emil MalucelliDepartment of Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.ORCID 0000-0002-1077-0098
University of Bologna · ITALBA Synchrotron (Spain) · ESIstituto Ortopedico Rizzoli · ITLaboratori Guglielmo Marconi (Italy) · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma (OS) is the most common primary malignant bone tumor and its etiology has recently been associated with osteogenic differentiation dysfunctions. OS cells keep a capacity for uncontrolled proliferation showing a phenotype similar to undifferentiated osteoprogenitors with abnormal biomineralization. Within this context, both conventional and X-ray synchrotron-based techniques have been exploited to deeply characterize the genesis and evolution of mineral depositions in a human OS cell line (SaOS-2) exposed to an osteogenic cocktail for 4 and 10 days. A partial restoration of the physiological biomineralization, culminating with the formation of hydroxyapatite, was observed at 10 days after treatment together with a mitochondria-driven mechanism for calcium transportation within the cell. Interestingly, during differentiation, mitochondria showed a change in morphology from elongated to rounded, indicating a metabolic reprogramming of OS cells possibly linked to an increase in glycolysis contribution to energy metabolism. These findings add a dowel to the genesis of OS giving new insights on the development of therapeutic strategies able to restore the physiological mineralization in OS cells.

Indexed as

Bone NeoplasmsOsteosarcomaBiomineralizationCell DifferentiationCell Line, TumorCell ProliferationHumansMitochondriaOsteogenesisbiomineralizationbone cancercalcium L-edgecryo-XANESmitochondriaosteoblastic differentiationosteogenic sarcoma

Identifiers

PMID37239904
PMCPMC10218373
OpenAlexW4376138665

What OpenQuestion holds

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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.