Evidence map›Paper›PMID 29198823›Full record

ArticleStem cell reports2017

microRNA-184 Induces a Commitment Switch to Epidermal Differentiation.

Sara Nagosa, Friederike Leesch, Daria Putin, Swarnabh Bhattacharya, Anna Altshuler, Laura Serror, Aya Amitai-Lange, Waseem Nasser, Edith Aberdam, Matthieu Rouleau and 4 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

34 citing papers in PubMed, 58 citations in OpenAlex.

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  20. Consequences of genetic variants in miRNA genes.Computational and structural biotechnology journal · 2022
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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

14 authors at 5 institutions in 3 countries.

Sara NagosaDepartment of Genetics and Developmental Biology, The Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 31096, Israel.
Friederike LeeschDepartment of Genetics and Developmental Biology, The Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 31096, Israel.
Daria PutinDepartment of Genetics and Developmental Biology, The Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 31096, Israel.
Swarnabh BhattacharyaDepartment of Genetics and Developmental Biology, The Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 31096, Israel.
Anna AltshulerDepartment of Genetics and Developmental Biology, The Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 31096, Israel.
Laura SerrorDepartment of Genetics and Developmental Biology, The Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 31096, Israel.
Aya Amitai-LangeDepartment of Genetics and Developmental Biology, The Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 31096, Israel.
Waseem NasserDepartment of Genetics and Developmental Biology, The Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 31096, Israel.
Edith AberdamUniversity Paris Diderot, Sorbonne Paris Cité, Paris 75475, France; INSERM U976, Hôpital St-Louis, Paris 75010, France.
Matthieu RouleauCNRS, LP2M, UMR7370, Faculté de Médecine, Nice, France; Université Nice Sophia Antipolis, Nice, France.
Sudhir G TattikotaMax Delbrueck Center for Molecular Medicine, Robert Roessle Strasse 10, Berlin 13125, Germany.
Matthew N PoyMax Delbrueck Center for Molecular Medicine, Robert Roessle Strasse 10, Berlin 13125, Germany.
Daniel AberdamUniversity Paris Diderot, Sorbonne Paris Cité, Paris 75475, France; INSERM U976, Hôpital St-Louis, Paris 75010, France.
Ruby Shalom-FeuersteinDepartment of Genetics and Developmental Biology, The Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 31096, Israel. Electronic address: shalomfe@tx.technion.ac.il.
Technion – Israel Institute of Technology · ILMax Delbrück Center · DEDélégation Paris 7 · FRInserm · FRUniversité Côte d'Azur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

miR-184 is a highly evolutionary conserved microRNA (miRNA) from fly to human. The importance of miR-184 was underscored by the discovery that point mutations in miR-184 gene led to corneal/lens blinding disease. However, miR-184-related function in vivo remained unclear. Here, we report that the miR-184 knockout mouse model displayed increased p63 expression in line with epidermal hyperplasia, while forced expression of miR-184 by stem/progenitor cells enhanced the Notch pathway and induced epidermal hypoplasia. In line, miR-184 reduced clonogenicity and accelerated differentiation of human epidermal cells. We showed that by directly repressing cytokeratin 15 (K15) and FIH1, miR-184 induces Notch activation and epidermal differentiation. The disease-causing miR-184

Indexed as

AnimalsBlindnessCell DifferentiationCell ProliferationEpidermisGene Expression Regulation, DevelopmentalHumansKeratin-15MiceMice, KnockoutMicroRNAsMixed Function OxygenasesPhosphoproteinsReceptors, NotchSignal TransductionStem Cellsfactor inhibiting hypoxia-inducible factor 1, mouseKeratin-15MicroRNAsMIRN184 microRNA, mouseMixed Function OxygenasesPhosphoproteinsReceptors, NotchTrans-ActivatorsTrp63 protein, mousecorneaepidermisFIH1hair follicleK15microRNAmiR-184miRNA-184notchstem cells

Identifiers

PMID29198823
PMCPMC5785777
OpenAlexW2775037127

What OpenQuestion holds

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LicenceCC BY
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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.