Evidence map›Paper›PMID 18637011›Full record

ArticleBrain pathology (Zurich, Switzerland)2009

Spontaneous in vitro transformation of adult neural precursors into stem-like cancer cells.

Florian A Siebzehnrubl, Ina Jeske, Dorit Müller, Rolf Buslei, Roland Coras, Eric Hahnen, Hagen B Huttner, Denis Corbeil, Johanna Kaesbauer, Thomas Appl and 2 more

Open access · greenAbstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Correlation of Musashi-1, Lgr5, and pEGFR expressions in human small intestinal adenocarcinomas.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Neurogenic astrocytes and their glycoconjugates: not just "glue" anymore.Methods in molecular biology (Clifton, N.J.) · 2012
    Review
  10. Article
  11. Article
  12. Risk factors in the development of stem cell therapy.Journal of translational medicine · 2011
    Article
  13. Article
  14. Article
  15. Article
  16. Cellular repair strategies in Parkinson's disease.Therapeutic advances in neurological disorders · 2009
    Article
  17. 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

12 authors at 1 institution in 1 country.

Florian A SiebzehnrublDepartment of Neuropathology. Franz-Penzoldt-Center, University of Erlangen-Nuremberg, Nuremberg, Germany. fas@ufl.edu
Ina Jeske
Dorit Müller
Rolf Buslei
Roland Coras
Eric Hahnen
Hagen B Huttner
Denis Corbeil
Johanna Kaesbauer
Thomas Appl
Stephan von Hörsten
Ingmar Blümcke
Friedrich-Alexander-Universität Erlangen-Nürnberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have found that cellular self-renewal capacity in brain cancer is heterogeneous, with only stem-like cells having this property. A link between adult stem cells and cancer stem cells remains, however, to be shown. Here, we describe the emergence of cancer stem-like cells from in vitro cultured brain stem cells. Adult rat subventricular zone (SVZ) stem cells transformed into tumorigenic cell lines after expansion in vitro. These cell lines maintained characteristic features of stem-like cells expressing Nestin, Musashi-1 and CD133, but continued to proliferate upon differentiation induction. Karyotyping detected multiple acquired chromosomal aberrations, and syngeneic transplantation into the brain of adult rats resulted in malignant tumor formation. Tumors revealed streak necrosis and displayed a neural as well as an undifferentiated phenotype. Deficient downregulation of platelet-derived growth factor (PDGF) receptor alpha was identified as candidate mechanism for tumor cell proliferation, and its knockdown by siRNA resulted in a reduction of cell growth. Our data point to adult brain precursor cells to be transformed in malignancies. Furthermore, in vitro expansion of adult neural stem cells, which will be mandatory for therapeutic strategies in neurological disorders, also harbors the risk for amplifying precursor cells with acquired genetic abnormalities and induction of malignant tumors after transplantation.

Indexed as

Adult Stem CellsAnimalsBlotting, WesternBrainBrain NeoplasmsBrain Tissue TransplantationCell DifferentiationCell Transformation, NeoplasticChromosome AberrationsImmunohistochemistryNeoplastic Stem CellsNeuronsRatsRats, WistarReceptor, Platelet-Derived Growth Factor alphaReverse Transcriptase Polymerase Chain ReactionReceptor, Platelet-Derived Growth Factor alphaRNA, Small Interfering

Identifiers

PMID18637011
PMCPMC8094744
OpenAlexW1975564296

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.