Evidence map›Paper›PMID 29253717›Full record

ArticleNeurobiology of aging2018

Regulation of ADAM10 by miR-140-5p and potential relevance for Alzheimer's disease.

Rumana Akhter, Yvonne Shao, McKenzie Shaw, Shane Formica, Maria Khrestian, James B Leverenz, Lynn M Bekris

Abstract read
In one paragraph

Article in Neurobiology of aging, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 20% 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

39 citing papers in PubMed, 2 syntheses or guidelines pooled it, 59 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

7 authors at 2 institutions in 1 country.

Rumana AkhterGenomic Medicine Institute, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA. Electronic address: akhterr@ccf.org.
Yvonne ShaoGenomic Medicine Institute, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA.
McKenzie ShawGenomic Medicine Institute, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA.
Shane FormicaGenomic Medicine Institute, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA.
Maria KhrestianGenomic Medicine Institute, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA.
James B LeverenzLou Ruvo Center for Brain Health, Neurological Institute, Cleveland Clinic, Cleveland, OH, USA.
Lynn M BekrisGenomic Medicine Institute, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA.
Cleveland Clinic · USLou Ruvo Brain Institute · US

Funding

THERAPEUTIC EFFECTS OF INTRA-NASAL INSULIN DETEMIRP50AG005136 · NIA · UNIVERSITY OF WASHINGTON · PI WIJSMAN, ELLEN M · 1985 to 2019
$57.2M
Biomarker Expression and Regulatory Haplotypes in Alzheimer's DiseaseR00AG034214 · NIA · UNIVERSITY OF WASHINGTON · PI BEKRIS, LYNN · 2012 to 2014
$725k
Biomarker Expression and Regulatory Haplotypes in Alzheimer's DiseaseK99AG034214 · NIA · UNIVERSITY OF WASHINGTON · PI BEKRIS, LYNN · 2010 to 2011
$254k
NIA NIH HHS K99 AG034214NIA NIH HHS P50 AG005136NIA NIH HHS R00 AG034214
6 · The paper itself

Abstract

Recent reports in Alzheimer's disease (AD) research suggest that alterations in microRNA (miRNA) expression are associated with disease pathology. Our previous studies suggest that A Disintegrin and Metalloproteinase 10 (ADAM10) expression is important in AD and could be modulated by an extended regulatory region that includes the 3' untranslated region. In this study, we have investigated the role of trans-acting factors in ADAM10 gene regulation. Our study shows that miRNA-140-5p has enhanced expression in the AD postmortem brain hippocampus using high-throughput miRNA arrays and quantitative real-time polymerase chain reaction. Interestingly, we have also seen that miRNA-140-5p seed sequence is present on 3' untranslated region of both ADAM10 and its transcription factor SOX2. The specific interaction of miRNA-140-5p with both ADAM10 and SOX2 signifies high regulatory importance of this miRNA in controlling ADAM10 expression. Thus, this investigation unravels mechanisms underlying ADAM10 downregulation by miR-140-5p and suggests that dysfunctional regulation of ADAM10 expression is exacerbated by AD-related neurotoxic effects. These findings underscore the importance of understanding the impact of trans-acting factors in the modulation of AD pathophysiology.

Indexed as

Genetic Association Studies3' Untranslated RegionsADAM10 ProteinAlzheimer DiseaseAmyloid Precursor Protein SecretasesCell LineDown-RegulationGene Expression RegulationHippocampusHumansMembrane ProteinsMicroRNAsOligonucleotide Array Sequence AnalysisReal-Time Polymerase Chain ReactionSOXB1 Transcription Factors3' Untranslated RegionsADAM10 ProteinADAM10 protein, humanAmyloid Precursor Protein SecretasesMembrane ProteinsMicroRNAsMirn140 microRNA, humanSOX2 protein, humanSOXB1 Transcription Factors

Identifiers

PMID29253717
PMCPMC5800962
OpenAlexW2770980986

What OpenQuestion holds

Textmetadata
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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.