Evidence map›Paper›PMID 35386318›Full record

ArticleBioactive materials2022

Slow degrading Mg-based materials induce tumor cell dormancy on an osteosarcoma-fibroblast coculture model.

Philipp Globig, Regine Willumeit-Römer, Fernanda Martini, Elisa Mazzoni, Bérengère J C Luthringer-Feyerabend

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Bioactive materials, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07395219 (Prospective Evaluation of the Safety and Efficacy of Transoral Incisionless Fundoplication 2.0 in the Management of Reflux), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 25% 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.

NCT07395219 enrolling by invitationnot on this mapstarted 2023, after this paper: background citation

Prospective Evaluation of the Safety and Efficacy of Transoral Incisionless Fundoplication 2.0 in the Management of Reflux: a European Registry

Typeobservational_patient_registrySponsorCleveland Clinic LondonRan2023 to 2030Enrolled500ConditionsGastro -Oesophagal Reflux, Laryngo-pharyngeal RefluxArmsTransoral incisionless fundoplication with or without concomitant hiatal hernia repair with the EsophyX device
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. MnOMaterials today. Bio · 2026
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. 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

5 authors at 2 institutions in 2 countries.

Philipp GlobigInstitute of Metallic Biomaterials, Helmholtz-Zentrum Hereon, 21502, Geesthacht, Germany.
Regine Willumeit-RömerInstitute of Metallic Biomaterials, Helmholtz-Zentrum Hereon, 21502, Geesthacht, Germany.
Fernanda MartiniDepartment of Medical Sciences, University of Ferrara, 44121, Ferrara, Italy.
Elisa MazzoniDepartment of Medical Sciences, University of Ferrara, 44121, Ferrara, Italy.
Bérengère J C Luthringer-FeyerabendInstitute of Metallic Biomaterials, Helmholtz-Zentrum Hereon, 21502, Geesthacht, Germany.
Helmholtz-Zentrum Hereon · DEUniversity of Ferrara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma is one of the most common cancers in young adults and is commonly treated using surgery and chemotherapy. During the past years, these therapy approaches improved but failed to ameliorate the outcomes. Therefore, novel, targeted therapeutic approaches should be established to enhance treatment success while preserving patient's quality of life. Recent studies suggest the application of degradable magnesium (Mg) alloys as orthopedic implants bearing a potential antitumor activity. Here, we examined the influence of Mg-based materials on an osteosarcoma-fibroblast coculture. Both, Mg and Mg-6Ag did not lead to tumor cell apoptosis at low degradation rates. Instead, the Mg-based materials induced cellular dormancy in the cancer cells indicated by a lower number of Ki-67 positive cancer cells and a higher p38 expression. This dormancy-like state could be reversed by reseeding on non-degrading glass slides but could not be provoked by inhibition of the protein kinase R-like endoplasmic reticulum kinase. By investigating the influence of the disjunct surface-near effects of the Mg degradation on cell proliferation, an increased pH was found to be a main initiator of Mg degradation-dependent tumor cell proliferation inhibition.

Indexed as

AlkalizationCancerKi-67Magnesium degradationpHProliferation inhibition

Identifiers

PMID35386318
PMCPMC8965722
OpenAlexW4200574963

What OpenQuestion holds

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Registered trials

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.