Evidence map›Paper›PMID 28304372›Full record

ArticleScientific reports2017

MicroRNAs miR-203-3p, miR-664-3p and miR-708-5p are associated with median strain lifespan in mice.

Benjamin P Lee, Ivana Burić, Anupriya George-Pandeth, Kevin Flurkey, David E Harrison, Rong Yuan, Luanne L Peters, George A Kuchel, David Melzer, Lorna W Harries

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

17 citing papers in PubMed, 27 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

10 authors at 3 institutions in 2 countries.

Benjamin P LeeRNA-mediated mechanisms of Disease, Institute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Devon, UK.
Ivana BurićRNA-mediated mechanisms of Disease, Institute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Devon, UK.
Anupriya George-PandethRNA-mediated mechanisms of Disease, Institute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Devon, UK.
Kevin FlurkeyThe Jackson Laboratory Nathan Shock Center of Excellence in the Basic Biology of Aging, Bar Harbor, Maine, USA.
David E HarrisonThe Jackson Laboratory Nathan Shock Center of Excellence in the Basic Biology of Aging, Bar Harbor, Maine, USA.
Rong YuanThe Jackson Laboratory Nathan Shock Center of Excellence in the Basic Biology of Aging, Bar Harbor, Maine, USA.
Luanne L PetersThe Jackson Laboratory Nathan Shock Center of Excellence in the Basic Biology of Aging, Bar Harbor, Maine, USA.
George A KuchelUConn Centre on Aging, University of Connecticut Health Centre, Farmington, Connecticut, USA.
David MelzerUConn Centre on Aging, University of Connecticut Health Centre, Farmington, Connecticut, USA.
Lorna W HarriesRNA-mediated mechanisms of Disease, Institute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Devon, UK.
University of Exeter · GBJackson Laboratory · USUConn Health · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
Interventions That Retard Mammalian AgingU01AG022308 · NIA · JACKSON LABORATORY · PI Ronny Korstanje · 2003 to 2026
$30.5M
Translational CoreP30AG038070 · NIA · JACKSON LABORATORY · PI Gary A Churchill · 2010 to 2026
$19.3M
NCI NIH HHS P30 CA034196NIA NIH HHS P30 AG038070NIA NIH HHS U01 AG022308Wellcome Trust WT097835MF
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are small non-coding RNA species that have been shown to have roles in multiple processes that occur in higher eukaryotes. They act by binding to specific sequences in the 3' untranslated region of their target genes and causing the transcripts to be degraded by the RNA-induced silencing complex (RISC). MicroRNAs have previously been reported to demonstrate altered expression in several aging phenotypes such as cellular senescence and age itself. Here, we have measured the expression levels of 521 small regulatory microRNAs (miRNAs) in spleen tissue from young and old animals of 6 mouse strains with different median strain lifespans by quantitative real-time PCR. Expression levels of 3 microRNAs were robustly associated with strain lifespan, after correction for multiple statistical testing (miR-203-3p [β-coefficient = -0.6447, p = 4.8 × 10

Indexed as

AnimalsGene Expression ProfilingGene Expression RegulationLongevityMice, Inbred StrainsMicroRNAsRNA, MessengerSignal TransductionMicroRNAsMIRN203 microRNA, mouseMIRN664 microRNA, mousemirn708 microRNA, mouseRNA, Messenger

Identifiers

PMID28304372
PMCPMC5356331
OpenAlexW2595176149

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.