Evidence map›Paper›PMID 26091048›Full record

ArticlePloS one2015

Dicer Is Required for Normal Cerebellar Development and to Restrain Medulloblastoma Formation.

Frederique Zindy, Youngsoo Lee, Daisuke Kawauchi, Olivier Ayrault, Leila Ben Merzoug, Yang Li, Peter J McKinnon, Martine F Roussel

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. The Non-coding Side of Medulloblastoma.Frontiers in cell and developmental biology · 2020
    Review
  7. Review
  8. Article
  9. Article
  10. The paradox of dicer in cancer.Molecular & cellular oncology · 2016
    Article
  11. Article
  12. Article
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

8 authors at 1 institution in 1 country.

Frederique ZindyDepartment of Tumor Cell Biology, St. Jude Children's Research Hospital, Memphis, TN, United States of America.
Youngsoo LeeDepartment of Genetics, St. Jude Children's Research Hospital, Memphis, TN, United States of America.
Daisuke KawauchiDepartment of Tumor Cell Biology, St. Jude Children's Research Hospital, Memphis, TN, United States of America.
Olivier AyraultDepartment of Tumor Cell Biology, St. Jude Children's Research Hospital, Memphis, TN, United States of America.
Leila Ben MerzougDepartment of Tumor Cell Biology, St. Jude Children's Research Hospital, Memphis, TN, United States of America.
Yang LiDepartment of Genetics, St. Jude Children's Research Hospital, Memphis, TN, United States of America.
Peter J McKinnonDepartment of Genetics, St. Jude Children's Research Hospital, Memphis, TN, United States of America.
Martine F RousselDepartment of Tumor Cell Biology, St. Jude Children's Research Hospital, Memphis, TN, United States of America.
St. Jude Children's Research Hospital · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
The DNA Damage Response and Tumorigenesis in the BrainP01CA096832 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI BAKER, SUZANNE J. · 2003 to 2025
$38.0M
ATM and DNA Damage in the Nervous SystemR01NS037956 · NINDS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI MCKINNON, PETER J · 1998 to 2022
$7.6M
ATM and DNA Damage in the Nervous SystemR56NS037956 · NINDS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI MCKINNON, PETER J · 2007 to 2007
$413k
NCI NIH HHS CA-096832NCI NIH HHS CA-21765NCI NIH HHS P01 CA096832NCI NIH HHS P30 CA021765NINDS NIH HHS NS-37956NINDS NIH HHS R01 NS037956NINDS NIH HHS R56 NS037956
6 · The paper itself

Abstract

Dicer, a ribonuclease III enzyme, is required for the maturation of microRNAs. To assess its role in cerebellar and medulloblastoma development, we genetically deleted Dicer in Nestin-positive neural progenitors and in mice lacking one copy for the Sonic Hedgehog receptor, Patched 1. We found that conditional loss of Dicer in mouse neural progenitors induced massive Trp53-independent apoptosis in all proliferative zones of the brain and decreased proliferation of cerebellar granule progenitors at embryonic day 15.5 leading to abnormal cerebellar development and perinatal lethality. Loss of one copy of Dicer significantly accelerated the formation of mouse medulloblastoma of the Sonic Hedgehog subgroup in Patched1-heterozygous mice. We conclude that Dicer is required for proper cerebellar development, and to restrain medulloblastoma formation.

Indexed as

AnimalsApoptosisCell LineCell Transformation, NeoplasticCerebellumCerebral CortexGene DeletionGene Knockout TechniquesMedulloblastomaMiceMice, TransgenicMicroRNAsNestinNeural Stem CellsPhenotypeRibonuclease IIIMicroRNAsNestinRibonuclease IIITumor Suppressor Protein p53

Identifiers

PMID26091048
PMCPMC4474721
OpenAlexW599137255

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.