Evidence map›Paper›PMID 24141309›Full record

ArticleNature neuroscience2013

A population of Nestin-expressing progenitors in the cerebellum exhibits increased tumorigenicity.

Peng Li, Fang Du, Larra W Yuelling, Tiffany Lin, Renata E Muradimova, Rossella Tricarico, Jun Wang, Grigori Enikolopov, Alfonso Bellacosa, Robert J Wechsler-Reya and 1 more

Open access · greenAbstract read
In one paragraph

Article in Nature neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

74 citing papers in PubMed, 110 citations in OpenAlex.

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  20. The mAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Article

14 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 1 country.

Peng Li1] Cancer Biology Program, Fox Chase Cancer Center, Temple University Health System, Philadelphia, Pennsylvania, USA. [2] Department of Clinical Biochemistry, Southwest Hospital, Third Military Medical University, Chongqing, China.
Fang Du
Larra W Yuelling
Tiffany Lin
Renata E Muradimova
Rossella Tricarico
Jun Wang
Grigori Enikolopov
Alfonso Bellacosa
Robert J Wechsler-Reya
Zeng-jie Yang
Fox Chase Cancer Center · USTemple University Health System · USCold Spring Harbor Laboratory · USDuke Medical Center · USDuke University Hospital · USNational Cancer Institute · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
Somatostatin analogues as countermeasures against intestinal radiation toxicityU19AI067798 · NIAID · DUKE UNIVERSITY · PI CHAO, NELSON J. · 2005 to 2024
$82.1M
TRAINING PROGRAM IN CANCER RESEARCHT32CA009035 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI CHERNOFF, JONATHAN · 1985 to 2020
$10.5M
The MED1 Protein in DNA Damage Response and RepairR01CA078412 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI BELLACOSA, ALFONSO · 2004 to 2014
$3.7M
Leukotriene-Induced Nestin Expression Promotes Medulloblastoma TumorigenesisR01CA178380 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI YANG, ZENG-JIE · 2014 to 2018
$1.9M
Stem Cells, Progenitors, and the Origin of MedulloblastomaR01CA122759 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI WECHSLER-REYA, ROBERT J. · 2009 to 2013
$1.8M
Control of Medulloblastoma Migration & Survival by Unc5cR01NS052323 · NINDS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI WECHSLER-REYA, ROBERT J. · 2006 to 2010
$1.8M
NCI NIH HHS 5T32CA009035-37NCI NIH HHS P30 CA006927NCI NIH HHS R01 CA078412NCI NIH HHS R01 CA122759NCI NIH HHS R01-CA122759NCI NIH HHS R01 CA178380NCI NIH HHS R01-CA178380NCI NIH HHS T32 CA009035NIAID NIH HHS U19 AI067798NIAID NIH HHS U19-AI067798NINDS NIH HHS R01 NS052323
6 · The paper itself

Abstract

It is generally believed that cerebellar granule neurons originate exclusively from granule neuron precursors (GNPs) in the external germinal layer (EGL). Here we identified a rare population of neuronal progenitors in mouse developing cerebellum that expresses Nestin. Although Nestin is widely considered a marker for multipotent stem cells, these Nestin-expressing progenitors (NEPs) are committed to the granule neuron lineage. Unlike conventional GNPs, which reside in the outer EGL and proliferate extensively, NEPs reside in the deep part of the EGL and are quiescent. Expression profiling revealed that NEPs are distinct from GNPs and, in particular, express markedly reduced levels of genes associated with DNA repair. Consistent with this, upon aberrant activation of Sonic hedgehog (Shh) signaling, NEPs exhibited more severe genomic instability and gave rise to tumors more efficiently than GNPs. These studies revealed a previously unidentified progenitor for cerebellar granule neurons and a cell of origin for medulloblastoma.

Indexed as

AnimalsAnimals, NewbornAntineoplastic Agents, HormonalBasic Helix-Loop-Helix ProteinsCell DifferentiationCell ProliferationCell Transformation, NeoplasticCerebellumGene Expression Regulation, NeoplasticHumansLuminescent ProteinsMiceMice, SCIDMice, TransgenicNestinNeuronsAntineoplastic Agents, HormonalAtoh1 protein, mouseBasic Helix-Loop-Helix Proteinsfluorescent protein 583Luminescent ProteinsNes protein, mouseNestinPatched ReceptorsReceptors, Cell SurfaceTamoxifen

Identifiers

PMID24141309
PMCPMC3845444
OpenAlexW1985615173

What OpenQuestion holds

Textmetadata
LicenceTDM
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.