Evidence map›Paper›PMID 31748917›Full record

ReviewCellular and molecular life sciences : CMLS2020

miR-378a: a new emerging microRNA in metabolism.

Ivo F Machado, João S Teodoro, Carlos M Palmeira, Anabela P Rolo

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
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

39 citing papers in PubMed.

  1. Trial
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  12. Research progress onFrontiers in pharmacology · 2024
    Review
  13. Review
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  15. Review
  16. Article
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  18. Article
  19. MicroRNAs as the Sentinels of Redox and Hypertrophic Signalling.International journal of molecular sciences · 2022
    Review
  20. 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

4 authors.

Ivo F MachadoDepartment of Life Sciences, Faculty of Sciences and Technology, University of Coimbra, Calçada Martim de Freitas, 3000-456, Coimbra, Portugal.
João S TeodoroDepartment of Life Sciences, Faculty of Sciences and Technology, University of Coimbra, Calçada Martim de Freitas, 3000-456, Coimbra, Portugal.
Carlos M PalmeiraDepartment of Life Sciences, Faculty of Sciences and Technology, University of Coimbra, Calçada Martim de Freitas, 3000-456, Coimbra, Portugal.
Anabela P RoloDepartment of Life Sciences, Faculty of Sciences and Technology, University of Coimbra, Calçada Martim de Freitas, 3000-456, Coimbra, Portugal. anpiro@ci.uc.pt.ORCID http://orcid.org/0000-0003-3535-9630

Funding

Fundação para a Ciência e a Tecnologia CEECIND/04400/2017Fundação para a Ciência e a Tecnologia POCI-01- 0145-FEDER-016770Fundação para a Ciência e a Tecnologia UID/NEU/04539/2013Fundo Regional para a Ciência e Tecnologia CENTRO-01-0145-FEDER-000012-HealthyAging2020
6 · The paper itself

Abstract

Metabolic diseases, such as type 2 diabetes or obesity, are the consequence of the disruption of the organism's metabolic pathways. The discovery of small non-coding RNAs-microRNAs (miRNAs)-as post-transcriptional gene regulators opened new doors for the development of novel strategies to combat said diseases. The two strands of miR-378a, miR-378a-3p, and miR-378a-5p are encoded in the Ppargc1b gene and have an active role in the regulation of several metabolic pathways such as mitochondrial metabolism and autophagy. Recent studies recognized miR-378a as an important regulator of energy and glucose homeostasis, highlighting it as a potential target for the improvement of metabolic dysregulation. In the present review, the current knowledge on miR-378a will be discussed with a particular emphasis on its biological functions and mechanisms of action in metabolism, mitochondria, and autophagy.

Indexed as

AutophagyCell ProliferationDiabetes Mellitus, Type 2Gene Expression RegulationHumansMetabolic DiseasesMetabolic Networks and PathwaysMicroRNAsMitochondriaObesityRNA-Binding ProteinsMicroRNAsMIRN378 microRNA, humanPPARGC1B protein, humanRNA-Binding ProteinsAutophagyMetabolic diseasesMetabolismmiR-378aMitochondria

Identifiers

PMID31748917
PMCPMC11104830

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.