Evidence map›Paper›PMID 26431550›Full record

ArticlePloS one2015

mTOR Activation by PI3K/Akt and ERK Signaling in Short ELF-EMF Exposed Human Keratinocytes.

Antonia Patruno, Mirko Pesce, Alfredo Grilli, Lorenza Speranza, Sara Franceschelli, Maria Anna De Lutiis, Giovina Vianale, Erica Costantini, Paolo Amerio, Raffaella Muraro and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.3field-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, 43 citations in OpenAlex.

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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

12 authors at 1 institution in 1 country.

Antonia PatrunoDepartment of Medicine and Aging Science, University "G. d'Annunzio", Chieti, Italy.
Mirko PesceDepartment of Psychological, Health and Territorial Sciences, University "G. D'Annunzio", Chieti, Italy.
Alfredo GrilliDepartment of Psychological, Health and Territorial Sciences, University "G. D'Annunzio", Chieti, Italy.
Lorenza SperanzaDepartment of Medicine and Aging Science, University "G. d'Annunzio", Chieti, Italy.
Sara FranceschelliDepartment of Medicine and Aging Science, University "G. d'Annunzio", Chieti, Italy.
Maria Anna De LutiisDepartment of Medicine and Aging Science, University "G. d'Annunzio", Chieti, Italy.
Giovina VianaleDepartment of Medical, Oral and Biotechnological Sciences, University "G. D'Annunzio", Chieti, Italy.
Erica CostantiniDepartment of Medical, Oral and Biotechnological Sciences, University "G. D'Annunzio", Chieti, Italy.
Paolo AmerioDepartment of Medicine and Aging Science, University "G. d'Annunzio", Chieti, Italy.
Raffaella MuraroDepartment of Medical, Oral and Biotechnological Sciences, University "G. D'Annunzio", Chieti, Italy.
Mario FelacoDepartment of Medicine and Aging Science, University "G. d'Annunzio", Chieti, Italy.
Marcella RealeDepartment of Medical, Oral and Biotechnological Sciences, University "G. D'Annunzio", Chieti, Italy.
University of Chieti-Pescara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several reports suggest that ELF-EMF exposures interact with biological processes including promotion of cell proliferation. However, the molecular mechanisms by which ELF-EMF controls cell growth are not completely understood. The present study aimed to investigate the effect of ELF-EMF on keratinocytes proliferation and molecular mechanisms involved. Effect of ELF-EMF (50 Hz, 1 mT) on HaCaT cell cycle and cells growth and viability was monitored by FACS analysis and BrdU assay. Gene expression profile by microarray and qRT-PCR validation was performed in HaCaT cells exposed or not to ELF-EMF. mTOR, Akt and MAPKs expressions were evaluated by Western blot analysis. In HaCaT cells, short ELF-EMF exposure modulates distinct patterns of gene expression involved in cell proliferation and in the cell cycle. mTOR activation resulted the main molecular target of ELF-EMF on HaCaT cells. Our data showed the increase of the canonical pathway of mTOR regulation (PI3K/Akt) and activation of ERK signaling pathways. Our results indicate that ELF-EMF selectively modulated the expression of multiple genes related to pivotal biological processes and functions that play a key role in physio-pathological mechanisms such as wound healing.

Indexed as

Cell Culture TechniquesCell ProliferationElectromagnetic FieldsHumansKeratinocytesMaleMAP Kinase Signaling SystemMiddle AgedMultigene FamilyPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionTOR Serine-Threonine KinasesTranscriptomeWound HealingMTOR protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinases

Identifiers

PMID26431550
PMCPMC4592237
OpenAlexW1872690706

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.