Evidence map›Paper›PMID 27195075›Full record

ArticleOxidative medicine and cellular longevity2016

Metformin Decreases Reactive Oxygen Species, Enhances Osteogenic Properties of Adipose-Derived Multipotent Mesenchymal Stem Cells In Vitro, and Increases Bone Density In Vivo.

Krzysztof Marycz, Krzysztof A Tomaszewski, Katarzyna Kornicka, Brandon Michael Henry, Sebastian Wroński, Jacek Tarasiuk, Monika Maredziak

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

50 citing papers in PubMed, 99 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Metformin and bone metabolism: unraveling their direct and indirect effects.Therapeutic advances in endocrinology and metabolism · 2025
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Krzysztof MaryczElectron Microscopy Laboratory, Wroclaw University of Environmental and Life Sciences, 5b Kozuchowska Street, 51-631 Wroclaw, Poland; Wroclaw Research Centre EIT+, 147 Stablowicka Street, 54-066 Wroclaw, Poland.
Krzysztof A TomaszewskiDepartment of Anatomy, Jagiellonian University Medical College, 12 Kopernika Street, 31-034 Krakow, Poland.
Katarzyna KornickaElectron Microscopy Laboratory, Wroclaw University of Environmental and Life Sciences, 5b Kozuchowska Street, 51-631 Wroclaw, Poland.
Brandon Michael HenryDepartment of Anatomy, Jagiellonian University Medical College, 12 Kopernika Street, 31-034 Krakow, Poland.
Sebastian WrońskiFaculty of Physics and Applied Computer Science, AGH University of Science and Technology, 30 Mickiewicza Street, 30059 Krakow, Poland.
Jacek TarasiukFaculty of Physics and Applied Computer Science, AGH University of Science and Technology, 30 Mickiewicza Street, 30059 Krakow, Poland.
Monika MaredziakWroclaw Research Centre EIT+, 147 Stablowicka Street, 54-066 Wroclaw, Poland; Department of Animal Physiology and Biostructure, Faculty of Veterinary Medicine, Wroclaw University of Environmental and Life Sciences, 31 Norwida Street, 50-375 Wroclaw, Poland.
Wrocław University of Environmental and Life Sciences · PLAGH University of Krakow · PLJagiellonian University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to its pleiotropic effects, the commonly used drug metformin has gained renewed interest among medical researchers. While metformin is mainly used for the treatment of diabetes, recent studies suggest that it may have further application in anticancer and antiaging therapies. In this study, we investigated the proliferative potential, accumulation of oxidative stress factors, and osteogenic and adipogenic differentiation potential of mouse adipose-derived stem cells (MuASCs) isolated from mice treated with metformin for 8 weeks. Moreover, we investigated the influence of metformin supplementation on mice bone density and bone element composition. The ASCs isolated from mice who were treated with metformin for 8 weeks showed highest proliferative potential, generated a robust net of cytoskeletal projections, had reduced expression of markers associated with cellular senescence, and decreased amount of reactive oxygen species in comparison to control group. Furthermore, we demonstrated that these cells possessed greatest osteogenic differentiation potential, while their adipogenic differentiation ability was reduced. We also demonstrated that metformin supplementation increases bone density in vivo. Our result stands as a valuable source of data regarding the in vivo influence of metformin on ASCs and bone density and supports a role for metformin in regenerative medicine.

Indexed as

AdipogenesisAdipose TissueAnimalsBone and BonesBone DensityBone Morphogenetic Protein 2Cell DifferentiationCells, CulturedCell SurvivalCellular SenescenceEnzyme-Linked Immunosorbent AssayImmunophenotypingMesenchymal Stem CellsMetforminMiceMice, Inbred C57BLBmp2 protein, mouseBone Morphogenetic Protein 2MetforminOsteocalcinOsteopontinReactive Oxygen SpeciesSuperoxide Dismutase

Identifiers

PMID27195075
PMCPMC4852347
OpenAlexW2337654505

What OpenQuestion holds

Textmetadata
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.