Evidence map›Paper›PMID 33386590›Full record

ArticleMolecular biology reports2021

Plant miR171 modulates mTOR pathway in HEK293 cells by targeting GNA12.

Angelo Gismondi, Valentina Nanni, Valentina Monteleone, Claudia Colao, Gabriele Di Marco, Antonella Canini

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

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  13. Looking for Plant microRNAs in Human Blood Samples: Bioinformatics Evidence and Perspectives.Plant foods for human nutrition (Dordrecht, Netherlands) · 2023
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  16. Inhibition of osteosarcoma by European Mistletoe derived val-miR218.Extracellular vesicles and circulating nucleic acids · 2023
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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

6 authors at 1 institution in 1 country.

Angelo GismondiDepartment of Biology, University of Rome "Tor Vergata", via della Ricerca Scientifica 1, 00133, Rome, Italy. gismondi@scienze.uniroma2.it.ORCID http://orcid.org/0000-0002-9257-9667
Valentina NanniDepartment of Biology, University of Rome "Tor Vergata", via della Ricerca Scientifica 1, 00133, Rome, Italy.
Valentina MonteleoneDepartment of Biology, University of Rome "Tor Vergata", via della Ricerca Scientifica 1, 00133, Rome, Italy.
Claudia ColaoDepartment of Biology, University of Rome "Tor Vergata", via della Ricerca Scientifica 1, 00133, Rome, Italy.
Gabriele Di MarcoDepartment of Biology, University of Rome "Tor Vergata", via della Ricerca Scientifica 1, 00133, Rome, Italy.
Antonella CaniniDepartment of Biology, University of Rome "Tor Vergata", via della Ricerca Scientifica 1, 00133, Rome, Italy. canini@uniroma2.it.
University of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plant microRNAs have shown the capacity to regulate mammalian systems. The potential bioactivity of miR171vr, an isoform of the plant miR171, on human embryonic kidney 293 (HEK293) cells was investigated. Bioinformatics simulations revealed that human G protein subunit alpha 12 (GNA12) transcript could represent an excellent target for miR171vr. To confirm this prediction, in vitro experiments were performed using a synthetic microRNA designed on miR171vr sequence. MiR-treated cells showed a significant decrease of GNA12 mRNA and protein levels, confirming the putative cross-kingdom interaction. In addition, miR171vr determined the modulation of GNA12 downstream signaling factors, including mTOR, as expected. Finally, the effect of the plant miRNA on HEK293 cell growth and its stability in presence of several stressors, such as those miming digestive processes and procedures for preparing food, were evaluated. All this preliminary evidence would suggest that miR171vr, introduced by diet or as supplement in gene therapies, could potentially influence human gene expression, especially for treating disorders where GNA12 is over-expressed (i.e. oral cancer, breast and prostate adenocarcinoma) or mTOR kinase is down-regulated (e.g. obesity, type 2 diabetes, neurodegeneration).

Indexed as

Cell ProliferationDiabetes Mellitus, Type 2Gene Expression Regulation, NeoplasticGTP-Binding Protein alpha Subunit, Gi2HEK293 CellsHumansMicroRNAsNeoplasmsObesityProtein Interaction MapsSignal TransductionTOR Serine-Threonine KinasesGTP-Binding Protein alpha Subunit, Gi2MicroRNAsMIRN171 microRNA, ArabidopsisMTOR protein, humanTOR Serine-Threonine KinasesBioactive food plantsCross-kingdom interactionDietGene therapyPlant microRNA

Identifiers

PMID33386590
OpenAlexW3113516346

What OpenQuestion holds

Textmetadata
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.