Evidence map›Paper›PMID 22202053›Full record

ReviewFrontiers in bioscience (Scholar edition)2012

The potential origin of glioblastoma initiating cells.

David A Chesler, Mitchell S Berger, Alfredo Quinones-Hinojosa

Abstract readReview
In one paragraph

Review in Frontiers in bioscience (Scholar edition), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

3 authors.

David A CheslerDepartment of Neurosurgery, University of Maryland Medical Center, Baltimore, MD 21212, USA.
Mitchell S Berger
Alfredo Quinones-Hinojosa

Funding

RESEARCH TRAINING IN NEURO-ONCOLOGY FOR NEUROSURGEONST32CA009574 · NCI · JOHNS HOPKINS UNIVERSITY · PI GROSSMAN, STUART A · 1987 to 2012
$2.6M
Role of NKCC1 on Brain Tumor Stem Cell Migration After EGF and Slit-2 StimulationR01NS070024 · NINDS · JOHNS HOPKINS UNIVERSITY · PI QUINONES-HINOJOSA, ALFREDO · 2010 to 2014
$2.4M
Migration of Human Neural Stem Cells In Vitro and In VivoK08NS055851 · NINDS · JOHNS HOPKINS UNIVERSITY · PI QUINONES-HINOJOSA, ALFREDO · 2006 to 2010
$880k
Howard Hughes Medical Institute 905675NCI NIH HHS T32 CA009574NINDS NIH HHS 1K08NS055851NINDS NIH HHS K08 NS055851NINDS NIH HHS R01 NS070024NINDS NIH HHS R01NS070024
6 · The paper itself

Abstract

Despite intensive clinical and laboratory research and effort, Glioblastoma remains the most common and invariably lethal primary cancer of the central nervous system. The identification of stem cell and lineage-restricted progenitor cell populations within the adult human brain in conjunction with the discovery of stem-like cells derived from gliomas which are themselves tumorigenic and have been shown to have properties of self-renewal and multipotency, has led to the hypothesis that this population of cells may represent glioma initiating cells. Extensive research characterizing the anatomic distribution and phenotype of neural stem cells in the adult brain, and the genetic underpinnings needed for malignant transformation may ultimately lead to the identification of the cellular origin for glioblastoma. Defining the cellular origin of this lethal disease may ultimately provide new therapeutic targets and modalities finally altering an otherwise bleak outcome for patients with glioblastoma.

Indexed as

AnimalsBrain NeoplasmsCell LineageCell Transformation, NeoplasticGlioblastomaHumansNeoplastic Stem Cells

Identifiers

PMID22202053
PMCPMC3635065

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.