Evidence map›Paper›PMID 25059231›Full record

ArticleActa neuropathologica communications2014

Genetic drivers of metastatic dissemination in sonic hedgehog medulloblastoma.

Noah C Jenkins, Ricky R Kalra, Adrian Dubuc, Walavan Sivakumar, Carolyn A Pedone, Xiaochong Wu, Michael D Taylor, Daniel W Fults

Open access · goldAbstract read
In one paragraph

Article in Acta neuropathologica communications, 2014. 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
1.4field-weighted citation impact, top 19% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

  1. GDI2 protein: research progress and its mechanisms in diseases.Frontiers in cell and developmental biology · 2026
    Review
  2. Review
  3. Review
  4. Small Fish, Big Answers: Zebrafish and the Molecular Drivers of Metastasis.International journal of molecular sciences · 2025
    Review
  5. TheInternational journal of molecular sciences · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Aging · 2021
    Article
  11. Article
  12. The molecular biology of medulloblastoma metastasis.Brain pathology (Zurich, Switzerland) · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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 4 institutions in 2 countries.

Noah C Jenkins
Ricky R Kalra
Adrian Dubuc
Walavan Sivakumar
Carolyn A Pedone
Xiaochong Wu
Michael D Taylor
Daniel W FultsDepartment of Neurosurgery, Clinical Neurosciences Center, University of Utah School of Medicine, 175 North Medical Drive East, Salt Lake City 84132, UT, USA. daniel.fults@hsc.utah.edu.
University of Utah · USBrigham and Women's Hospital · USHospital for Sick Children · CAUniversity of Toronto · CA

Funding

Mouse models to discover new drivers of medulloblastomaR01CA159859 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI Michael D. Taylor, WILLIAM A WEISS · 2011 to 2026
$10.4M
Medulloblastoma and MetastasesR01CA148699 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TAYLOR, MICHAEL D., WEISS, WILLIAM A · 2010 to 2014
$2.4M
SOMATIC CELL TRANSFER TO MODEL MEDULLOBLASTOMA IN MICER01CA108622 · NCI · UNIVERSITY OF UTAH · PI FULTS, DANIEL WEBSTER · 2005 to 2013
$2.0M
NCI NIH HHS CA108622NCI NIH HHS CA148699NCI NIH HHS CA159859NCI NIH HHS R01 CA108622NCI NIH HHS R01 CA148699NCI NIH HHS R01 CA159859
6 · The paper itself

Abstract

Leptomeningeal dissemination (LMD), the metastatic spread of tumor cells via the cerebrospinal fluid to the brain and spinal cord, is an ominous prognostic sign for patients with the pediatric brain tumor medulloblastoma. The need to reduce the risk of LMD has driven the development of aggressive treatment regimens, which cause disabling neurotoxic side effects in long-term survivors. Transposon-mediated mutagenesis studies in mice have revealed numerous candidate metastasis genes. Understanding how these genes drive LMD will require functional assessment using in vivo and cell culture models of medulloblastoma. We analyzed two genes that were sites of frequent transposon insertion and highly expressed in human medulloblastomas: Arnt (aryl hydrocarbon receptor nuclear translocator) and Gdi2 (GDP dissociation inhibitor 2). Here we show that ectopic expression of Arnt and Gdi2 promoted LMD in mice bearing Sonic hedgehog (Shh)-induced medulloblastomas. We overexpressed Arnt and Gdi2 in a human medulloblastoma cell line (DAOY) and an immortalized, nontransformed cell line derived from mouse granule neuron precursors (SHH-NPD) and quantified migration, invasiveness, and anchorage-independent growth, cell traits that are associated with metastatic competence in carcinomas. In SHH-NPD cells. Arnt and Gdi2 stimulated all three traits. In DAOY cells, Arnt had the same effects, but Gdi2 stimulated invasiveness only. These results support a mechanism whereby Arnt and Gdi2 cause cells to detach from the primary tumor mass by increasing cell motility and invasiveness. By conferring to tumor cells the ability to proliferate without surface attachment, Arnt and Gdi2 favor the formation of stable colonies of cells capable of seeding the leptomeninges.

Indexed as

MedulloblastomaAnimalsAryl Hydrocarbon Receptor Nuclear TranslocatorCell Line, TumorCell MovementCerebellar NeoplasmsGene Transfer TechniquesGuanine Nucleotide Dissociation InhibitorsHedgehog ProteinsHumansMeningeal NeoplasmsMiceMice, TransgenicMutagenesis, InsertionalMutationNeoplasm MetastasisAryl Hydrocarbon Receptor Nuclear TranslocatorGDI2 protein, humanGuanine Nucleotide Dissociation InhibitorsHedgehog ProteinsSHH protein, human

Identifiers

PMID25059231
PMCPMC4149244
OpenAlexW2137804322

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.