Evidence map›Paper›PMID 28401018›Full record

ReviewAmerican journal of cancer research2017

OTX2 expression contributes to proliferation and progression in Myc-amplified medulloblastoma.

Yining Lu, Collin M Labak, Neha Jain, Ian J Purvis, Maheedhara R Guda, Sarah E Bach, Andrew J Tsung, Swapna Asuthkar, Kiran K Velpula

Open access · greenAbstract readReview
In one paragraph

Review in American journal of cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 25% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
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  10. iScience · 2023
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  16. Research progress in molecular pathology markers in medulloblastoma.Exploration of targeted anti-tumor therapy · 2023
    Review
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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

9 authors at 1 institution in 1 country.

Yining LuDepartment of Cancer Biology and Pharmacology, College of Medicine, University of Illinois Peoria 61656, IL, U. S. A.
Collin M LabakDepartment of Cancer Biology and Pharmacology, College of Medicine, University of Illinois Peoria 61656, IL, U. S. A.
Neha JainDepartment of Cancer Biology and Pharmacology, College of Medicine, University of Illinois Peoria 61656, IL, U. S. A.
Ian J PurvisDepartment of Cancer Biology and Pharmacology, College of Medicine, University of Illinois Peoria 61656, IL, U. S. A.
Maheedhara R GudaDepartment of Cancer Biology and Pharmacology, College of Medicine, University of Illinois Peoria 61656, IL, U. S. A.
Sarah E BachDepartment of Pathology, College of Medicine, University of Illinois Peoria 61656, IL, U. S. A.
Andrew J TsungDepartment of Cancer Biology and Pharmacology, College of Medicine, University of IllinoisPeoria 61656, IL, U. S. A.; Department of Neurosurgery, College of Medicine, University of IllinoisPeoria 61656, IL, U. S. A.; Illinois Neurological InstitutePeoria 61656, IL, U. S. A.
Swapna AsuthkarDepartment of Cancer Biology and Pharmacology, College of Medicine, University of Illinois Peoria 61656, IL, U. S. A.
Kiran K VelpulaDepartment of Cancer Biology and Pharmacology, College of Medicine, University of IllinoisPeoria 61656, IL, U. S. A.; Department of Neurosurgery, College of Medicine, University of IllinoisPeoria 61656, IL, U. S. A.
Illinois College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Medulloblastoma is one of the most prevalent pediatric brain malignancies, accounting for approximately 20% of all primary CNS tumors in children under the age of 19. OTX2 is the member of a highly conserved family of bicoid-like homeodomain transcription factors responsible for the regulation of cerebellar development and of current investigational interest in the tumorigenesis of medulloblastoma. Recent studies have revealed that Group 3 and Group 4 medulloblastomas show marked overexpression of OTX2 with a concurrent amplification of the MYC and MYCN oncogenes, respectively, correlating with anaplasticity and unfavorable patient outcomes. More recent attempts at elucidating the mechanism of OTX2-driven oncogenesis at the cellular level has also revealed that OTX2 may confer stem-cell like properties to tumor cells via epigenetic regulation. The review seeks to define the interaction pathways and binding partners involved in OTX2 function, its usefulness as a molecular marker for risk stratification and prognosis, and the mechanism by which it drives tumor maintenance. Additionally, it will preview unpublished data by our group highlighting the unanticipated involvement of OTX2 in the control of cellular metabolism.

Indexed as

cancer metabolismhistone modificationmedulloblastomaMYCOTX2

Identifiers

PMID28401018
PMCPMC5385649
OpenAlexW2613047032

What OpenQuestion holds

Textmetadata
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.