Evidence map›Paper›PMID 28493990›Full record

ArticlePloS one2017

MiR-338-3p regulates neuronal maturation and suppresses glioblastoma proliferation.

James R Howe, Emily S Li, Sarah E Streeter, Gilbert J Rahme, Edmond Chipumuro, Grace B Russo, Julia F Litzky, L Benjamin Hills, Kyla R Rodgers, Patrick D Skelton and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Small Differences and Big Changes: The Many Variables of MicroRNA Expression and Function in the Brain.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Circulating RNAs as Potential Biomarkers in Amyotrophic Lateral Sclerosis.International journal of molecular sciences · 2020
    Review
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.

James R HoweDepartment of Physiology and Neurobiology, Geisel School of Medicine at Dartmouth College, Lebanon, New Hampshire, United States of America.
Emily S LiDepartment of Physiology and Neurobiology, Geisel School of Medicine at Dartmouth College, Lebanon, New Hampshire, United States of America.
Sarah E StreeterDepartment of Physiology and Neurobiology, Geisel School of Medicine at Dartmouth College, Lebanon, New Hampshire, United States of America.
Gilbert J RahmeDepartment of Genetics, Geisel School of Medicine at Dartmouth College, Lebanon, New Hampshire, United States of America.
Edmond ChipumuroDepartment of Physiology and Neurobiology, Geisel School of Medicine at Dartmouth College, Lebanon, New Hampshire, United States of America.
Grace B RussoDepartment of Physiology and Neurobiology, Geisel School of Medicine at Dartmouth College, Lebanon, New Hampshire, United States of America.
Julia F LitzkyDepartment of Physiology and Neurobiology, Geisel School of Medicine at Dartmouth College, Lebanon, New Hampshire, United States of America.
L Benjamin HillsDepartment of Physiology and Neurobiology, Geisel School of Medicine at Dartmouth College, Lebanon, New Hampshire, United States of America.
Kyla R RodgersDepartment of Physiology and Neurobiology, Geisel School of Medicine at Dartmouth College, Lebanon, New Hampshire, United States of America.
Patrick D SkeltonDepartment of Physiology and Neurobiology, Geisel School of Medicine at Dartmouth College, Lebanon, New Hampshire, United States of America.
Bryan W LuikartDepartment of Physiology and Neurobiology, Geisel School of Medicine at Dartmouth College, Lebanon, New Hampshire, United States of America.ORCID http://orcid.org/0000-0002-3181-6075
Dartmouth College · US

Funding

The Impact of PTEN Signaling on Neuronal Form and FunctionR01MH097949 · NIMH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BRYAN W LUIKART · 2012 to 2026
$7.4M
NIMH NIH HHS R01 MH097949
6 · The paper itself

Abstract

Neurogenesis is a highly-regulated process occurring in the dentate gyrus that has been linked to learning, memory, and antidepressant efficacy. MicroRNAs (miRNAs) have been previously shown to play an important role in the regulation of neuronal development and neurogenesis in the dentate gyrus via modulation of gene expression. However, this mode of regulation is both incompletely described in the literature thus far and highly multifactorial. In this study, we designed sensors and detected relative levels of expression of 10 different miRNAs and found miR-338-3p was most highly expressed in the dentate gyrus. Comparison of miR-338-3p expression with neuronal markers of maturity indicates miR-338-3p is expressed most highly in the mature neuron. We also designed a viral "sponge" to knock down in vivo expression of miR-338-3p. When miR-338-3p is knocked down, neurons sprout multiple primary dendrites that branch off of the soma in a disorganized manner, cellular proliferation is upregulated, and neoplasms form spontaneously in vivo. Additionally, miR-338-3p overexpression in glioblastoma cell lines slows their proliferation in vitro. Further, low miR-338-3p expression is associated with increased mortality and disease progression in patients with glioblastoma. These data identify miR-338-3p as a clinically relevant tumor suppressor in glioblastoma.

Indexed as

Cell DifferentiationAnimalsBrain NeoplasmsCell Line, TumorCell ProliferationCell ShapeDentate GyrusDisease-Free SurvivalGene Expression Regulation, NeoplasticGene Knockdown TechniquesGlial Fibrillary Acidic ProteinGlioblastomaHumansMice, Inbred C57BLMicroRNAsNeuronsGlial Fibrillary Acidic ProteinMicroRNAsMIRN338 microRNA, human

Identifiers

PMID28493990
PMCPMC5426787
OpenAlexW2612054083

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.