Evidence map›Paper›PMID 24349533›Full record

ArticlePloS one2013

Periostin responds to mechanical stress and tension by activating the MTOR signaling pathway.

Luciana K Rosselli-Murai, Luciana O Almeida, Chiara Zagni, Pablo Galindo-Moreno, Miguel Padial-Molina, Sarah L Volk, Marcelo J Murai, Hector F Rios, Cristiane H Squarize, Rogerio M Castilho

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Feeling the Heat. Mapping the Epigenetic Modifications of Histone during Burn Wound Healing.Journal of burn care & research : official publication of the American Burn Association · 2024
    Article
  9. The role of periostin in cardiac fibrosis.Heart failure reviews · 2024
    Review
  10. Review
  11. Article
  12. mTOR Signaling Components in Tumor Mechanobiology.International journal of molecular sciences · 2022
    Review
  13. Frontiers in molecular neuroscience · 2022
    Review
  14. Article
  15. Expression of Musashi-1 Increases in Bone Healing.International journal of molecular sciences · 2021
    Article
  16. Article
  17. Review
  18. Observational
  19. Article
  20. Topical delivery of mTOR inhibitor halts scarring.Journal of dermatological science · 2019
    Article
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

10 authors at 3 institutions in 2 countries.

Luciana K Rosselli-MuraiLaboratory of Epithelial Biology, Department of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, United States of America.
Luciana O AlmeidaLaboratory of Epithelial Biology, Department of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, United States of America.
Chiara ZagniLaboratory of Epithelial Biology, Department of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, United States of America.
Pablo Galindo-MorenoDepartment of Oral Surgery and Implant Dentistry, School of Dentistry, University of Granada, Granada, Spain.
Miguel Padial-MolinaDepartment of Oral Surgery and Implant Dentistry, School of Dentistry, University of Granada, Granada, Spain ; Department of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, United States of America.
Sarah L VolkDepartment of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, United States of America.
Marcelo J MuraiThe Division of Hematology and Oncology, University of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan, United States of America.
Hector F RiosDepartment of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, United States of America.
Cristiane H SquarizeLaboratory of Epithelial Biology, Department of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, United States of America.
Rogerio M CastilhoLaboratory of Epithelial Biology, Department of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, United States of America.
Michigan United · USUniversity of Michigan–Ann Arbor · USUniversidad de Granada · ES

Funding

Therapeutic Potential and Mechanism of Action of Potent Small Molecule InhibitorsP50CA097248 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WOLF, GREGORY T · 2002 to 2013
$25.3M
NCI NIH HHS P50 CA097248NCI NIH HHS P50-CA97248
6 · The paper itself

Abstract

Current knowledge about Periostin biology has expanded from its recognized functions in embryogenesis and bone metabolism to its roles in tissue repair and remodeling and its clinical implications in cancer. Emerging evidence suggests that Periostin plays a critical role in the mechanism of wound healing; however, the paracrine effect of Periostin in epithelial cell biology is still poorly understood. We found that epithelial cells are capable of producing endogenous Periostin that, unlike mesenchymal cell, cannot be secreted. Epithelial cells responded to Periostin paracrine stimuli by enhancing cellular migration and proliferation and by activating the mTOR signaling pathway. Interestingly, biomechanical stimulation of epithelial cells, which simulates tension forces that occur during initial steps of tissue healing, induced Periostin production and mTOR activation. The molecular association of Periostin and mTOR signaling was further dissected by administering rapamycin, a selective pharmacological inhibitor of mTOR, and by disruption of Raptor and Rictor scaffold proteins implicated in the regulation of mTORC1 and mTORC2 complex assembly. Both strategies resulted in ablation of Periostin-induced mitogenic and migratory activity. These results indicate that Periostin-induced epithelial migration and proliferation requires mTOR signaling. Collectively, our findings identify Periostin as a mechanical stress responsive molecule that is primarily secreted by fibroblasts during wound healing and expressed endogenously in epithelial cells resulting in the control of cellular physiology through a mechanism mediated by the mTOR signaling cascade.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCarrier ProteinsCell Adhesion MoleculesCell Line, TransformedCell MovementCell ProliferationEpithelial CellsFibroblastsHumansMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2Mechanotransduction, CellularMiceMultiprotein ComplexesRapamycin-Insensitive Companion of mTOR ProteinAdaptor Proteins, Signal TransducingCarrier ProteinsCell Adhesion MoleculesMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2mTOR protein, mouseMultiprotein ComplexesPostn protein, mouseRapamycin-Insensitive Companion of mTOR ProteinRegulatory-Associated Protein of mTORrictor protein, mouseRptor protein, mouseTOR Serine-Threonine Kinases

Identifiers

PMID24349533
PMCPMC3862800
OpenAlexW2128491331

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.