Evidence map›Paper›PMID 39191864›Full record

ArticleCommunications biology2024

miR-29 is an important driver of aging-related phenotypes.

Vijay Swahari, Ayumi Nakamura, Emilie Hollville, Yu-Han Hung, Matt Kanke, C Lisa Kurtz, Xurde M Caravia, David Roiz-Valle, Shenghui He, Janakiraman Krishnamurthy and 9 more

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
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  3. Extracellular vesicles and epigenetic aging clocks in tissue aging: an exosome-focused conceptual framework with a focus on skin.The journals of gerontology. Series A, Biological sciences and medical sciences · 2026
    Review
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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

19 authors.

Vijay Swahari *Neuroscience Center; University of North Carolina, Chapel Hill, NC, USA.
Ayumi Nakamura *Neuroscience Center; University of North Carolina, Chapel Hill, NC, USA.
Emilie Hollville *Neuroscience Center; University of North Carolina, Chapel Hill, NC, USA.ORCID 0000-0001-5711-8542
Yu-Han HungDepartment of Biomedical Sciences; College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Matt KankeDepartment of Biomedical Sciences; College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
C Lisa KurtzDepartment of Genetics; University of North Carolina, Chapel Hill, NC, USA.
Xurde M CaraviaDepartamento de Bioquímica y Biología Molecular, Instituto Universitario de Oncología (IUOPA), Universidad de Oviedo, Oviedo, Spain.ORCID 0000-0002-1173-7003
David Roiz-ValleDepartamento de Bioquímica y Biología Molecular, Instituto Universitario de Oncología (IUOPA), Universidad de Oviedo, Oviedo, Spain.ORCID 0000-0001-9131-6155
Shenghui HeDepartment of Genetics; University of North Carolina, Chapel Hill, NC, USA.
Janakiraman KrishnamurthyDepartment of Genetics; University of North Carolina, Chapel Hill, NC, USA.
Sahil KapoorNeuroscience Center; University of North Carolina, Chapel Hill, NC, USA.
Varun PrasadNeuroscience Center; University of North Carolina, Chapel Hill, NC, USA.
Cornelius FlowersNeuroscience Center; University of North Carolina, Chapel Hill, NC, USA.
Matt BeckNeuroscience Center; University of North Carolina, Chapel Hill, NC, USA.
Jeanette Baran-GaleDepartment of Genetics; University of North Carolina, Chapel Hill, NC, USA.
Norman SharplessDepartment of Genetics; University of North Carolina, Chapel Hill, NC, USA.ORCID 0000-0001-7078-9455
Carlos López-OtínDepartamento de Bioquímica y Biología Molecular, Instituto Universitario de Oncología (IUOPA), Universidad de Oviedo, Oviedo, Spain.ORCID 0000-0001-6964-1904
Praveen SethupathyDepartment of Biomedical Sciences; College of Veterinary Medicine, Cornell University, Ithaca, NY, USA. pr46@cornell.edu.ORCID 0000-0001-9887-8871
Mohanish DeshmukhNeuroscience Center; University of North Carolina, Chapel Hill, NC, USA. mohanish@med.unc.edu.ORCID 0000-0002-2597-5862

Funding

Essential Function of miR-29 in the Mature BrainR01AG055304 · NIA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DESHMUKH, MOHANISH P · 2017 to 2021
$2.6M
miR-29: A brain homeostasis molecule for Alzheimer’s disease preventionR01AG082140 · NIA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Mohanish P Deshmukh · 2023 to 2026
$2.5M
Molecular and Biological Functions of miR-29 in Lipid HomeostasisR01DK105965 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SETHUPATHY, PRAVEEN · 2016 to 2019
$1.4M
American Diabetes Association (ADA) 1-16-ACE-47NIA NIH HHS R01 AG055304NIA NIH HHS R01 AG082140NIDDK NIH HHS R01 DK105965U.S. Department of Health & Human Services | National Institutes of Health (NIH) AG055304U.S. Department of Health & Human Services | National Institutes of Health (NIH) AG082140U.S. Department of Health & Human Services | National Institutes of Health (NIH) DK105965
6 · The paper itself

Abstract

Aging is a consequence of complex molecular changes, but whether a single microRNA (miRNA) can drive aging remains unclear. A miRNA known to be upregulated during both normal and premature aging is miR-29. We find miR-29 to also be among the top miRNAs predicted to drive aging-related gene expression changes. We show that partial loss of miR-29 extends the lifespan of Zmpste24

Indexed as

AgingMicroRNAsPhenotypeAnimalsGene Expression RegulationLongevityMaleMembrane ProteinsMetalloendopeptidasesMiceMice, Inbred C57BLMice, KnockoutProgeriaMembrane ProteinsMetalloendopeptidasesMicroRNAsMIRN29 microRNA, mouseZmpste24 protein, mouse

Identifiers

PMID39191864
PMCPMC11349983

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.