Evidence map›Paper›PMID 33117266›Full record

ArticleFrontiers in neurology2020

Advances and Challenges in Understanding MicroRNA Function in Tauopathies: A Case Study of miR-132/212.

Emmanuelle Boscher, Julia Hernandez-Rapp, Serena Petry, Remi Keraudren, Sara Rainone, Andréanne Loiselle, Claudia Goupil, Andréanne Turgeon, Isabelle St-Amour, Emmanuel Planel and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 52% 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

6 citing papers in PubMed, 8 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

11 authors at 1 institution in 1 country.

Emmanuelle BoscherAxe Neurosciences, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.
Julia Hernandez-RappAxe Neurosciences, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.
Serena PetryAxe Neurosciences, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.
Remi KeraudrenAxe Neurosciences, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.
Sara RainoneAxe Neurosciences, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.
Andréanne LoiselleAxe Neurosciences, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.
Claudia GoupilAxe Neurosciences, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.
Andréanne TurgeonAxe Neurosciences, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.
Isabelle St-AmourAxe Neurosciences, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.
Emmanuel PlanelAxe Neurosciences, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.
Sébastien S HébertAxe Neurosciences, Centre de Recherche du CHU de Québec-Université Laval, Québec, QC, Canada.
Université Laval · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the past decade, several groups have reported that microRNAs (miRNAs) can participate in the regulation of tau protein at different levels, including its expression, alternative splicing, phosphorylation, and aggregation. These observations are significant, since the abnormal regulation and deposition of tau is associated with nearly 30 neurodegenerative disorders. Interestingly, miRNA profiles go awry in tauopathies such as Alzheimer's disease, progressive supranuclear palsy, and frontotemporal dementia. Understanding the role and impact of miRNAs on tau biology could therefore provide important insights into disease risk, diagnostics, and perhaps therapeutics. In this Perspective article, we discuss recent advances in miRNA research related to tau. While proof-of-principle studies hold promise, physiological validation remains limited. To help fill this gap, we describe herein a pure tauopathy mouse model deficient for the miR-132/212 cluster. This miRNA family is strongly downregulated in human tauopathies and shown to regulate tau

Indexed as

microRNAmiR-132PS19tautauopathies

Identifiers

PMID33117266
PMCPMC7553085
OpenAlexW3089804814

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.