Evidence map›Paper›PMID 20028867›Full record

ArticleCancer research2010

OTX2 is critical for the maintenance and progression of Shh-independent medulloblastomas.

David C Adamson, Qun Shi, Matthew Wortham, Paul A Northcott, Chunhui Di, Christopher G Duncan, Jianjun Li, Roger E McLendon, Darell D Bigner, Michael D Taylor and 1 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 2 pooled it
4.4field-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, 2 syntheses or guidelines pooled it, 125 citations in OpenAlex.

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  14. TheInternational journal of molecular sciences · 2024
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14 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

David C AdamsonDepartment of Surgery, The Pediatric Brain Tumor Foundation Institute, and The Preston Robert Tisch Brain Tumor Center at Duke, Duke University Medical Center, Veterans Affairs Medical Center, Durham, North Carolina 27710, USA.
Qun Shi
Matthew Wortham
Paul A Northcott
Chunhui Di
Christopher G Duncan
Jianjun Li
Roger E McLendon
Darell D Bigner
Michael D Taylor
Hai Yan
Duke University Hospital · USPediatric Brain Tumor Foundation · US

Funding

The Role of OTX2 in Molecular Pathogenesis of MedulloblastomaR01CA118822 · NCI · DUKE UNIVERSITY · PI YAN, HAI · 2006 to 2010
$1.2M
NCI NIH HHS R01 CA118822NCI NIH HHS R01CA118822
6 · The paper itself

Abstract

OTX2 is a developmentally regulated transcription factor involved in early morphogenesis of the central nervous system. This gene is amplified and overexpressed in medulloblastoma cell lines, but the nature and extent of its genetic alterations in primary tumors have not been evaluated. Analysis of a large cohort of primary medulloblastomas revealed frequent focal copy number gain of a region minimally containing OTX2 as a single gene. OTX2 copy number gain was restricted to tumor subtypes that did not express a molecular signature of Wnt or Shh pathway activation. FISH analysis revealed copy number gain in a subset of cells within medulloblastoma samples, suggesting a late event in tumor progression. Gain of OTX2 copy number was associated with the presence of anaplastic histologic features and shorter survival in medulloblastoma patients. In support of a functional role, ectopic OTX2 expression enhanced proliferation and tumorigenicity of immortalized primary cells, whereas OTX2 knockdown in medulloblastoma cells prolonged the survival of animals bearing xenograft tumors. Mechanistic investigations revealed upregulation of MYC as a potential mechanism whereby OTX2 promotes tumor progression. Our findings define OTX2 as an important oncogenic driver in medulloblastoma.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBlotting, WesternCerebellar NeoplasmsDisease ProgressionGene DosageGenes, mycHedgehog ProteinsHumansIn Situ Hybridization, FluorescenceMedulloblastomaMiceMice, NudeOligonucleotide Array Sequence AnalysisOtx Transcription FactorsPolymerase Chain ReactionHedgehog ProteinsOTX2 protein, humanOtx Transcription FactorsSHH protein, human

Identifiers

PMID20028867
PMCPMC2943736
OpenAlexW2141541918

What OpenQuestion holds

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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.