Evidence map›Paper›PMID 19834489›Full record

ArticleCell death and differentiation2010

IGF-IR-dependent expression of Survivin is required for T-antigen-mediated protection from apoptosis and proliferation of neural progenitors.

E Gualco, K Urbanska, G Perez-Liz, T Sweet, F Peruzzi, K Reiss, L Del Valle

Open access · bronzeAbstract read
In one paragraph

Article in Cell death and differentiation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. The Role of the JC Virus in Central Nervous System Tumorigenesis.International journal of molecular sciences · 2020
    Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Nuclear IRS-1 and cancer.Journal of cellular physiology · 2012
    Review
  15. Isolation and culture of rat embryonic neural cells: a quick protocol.Journal of visualized experiments : JoVE · 2012
    Article
  16. 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

7 authors at 1 institution in 1 country.

E GualcoDepartment of Neuroscience, Center for Neurovirology, Temple University School of Medicine, Philadelphia, PA, USA.
K Urbanska
G Perez-Liz
T Sweet
F Peruzzi
K Reiss
L Del Valle
Temple University · US

Funding

Nuclear IRS-1-DNA repair and mutagenesis in medulloblastomaR01CA095518 · NCI · TEMPLE UNIV OF THE COMMONWEALTH · PI REISS, KRZYSZTOF · 2002 to 2012
$2.6M
Involvement of Survivin in the Development of PMLR01NS055644 · NINDS · TEMPLE UNIV OF THE COMMONWEALTH · PI DEL VALLE, LUIS · 2007 to 2011
$1.5M
NCI NIH HHS R01 CA095518NINDS NIH HHS R01 NS055644
6 · The paper itself

Abstract

The insulin-like growth factor-1 receptor (IGF-IR) and the human polyomavirus JCV protein, T-antigen cooperate in the transformation of neuronal precursors in the cerebellum, which may be a contributing factor in the development of brain tumors. Because it is not clear why T-antigen requires IGF-IR for transformation, we investigated this process in neural progenitors from IGF-IR knockout embryos (ko-IGF-IR) and from their wild-type nontransgenic littermates (wt-IGF-IR). In contrast to wt-IGF-IR, the brain and dorsal root ganglia of ko-IGF-IR embryos showed low levels of the antiapoptotic protein Survivin, accompanied by elevated numbers of apoptotic neurons and an earlier differentiation phenotype. In wt-IGF-IR neural progenitors in vitro, induction of T-antigen expression tripled the expression of Survivin and accelerated cell proliferation. In ko-IGF-IR progenitors induction of T-antigen failed to increase Survivin, resulting in massive apoptosis. Importantly, ectopic expression of Survivin protected ko-IGF-IR progenitor cells from apoptosis and siRNA inhibition of Survivin activated apoptosis in wt-IGF-IR progenitors expressing T-antigen. Our results indicate that reactivation of the antiapoptotic Survivin may be a critical step in JCV T-antigen-induced transformation, which in neural progenitors requires IGF-IR.

Indexed as

Cell ProliferationAnimalsAntigens, Polyomavirus TransformingApoptosisCells, CulturedChildEmbryo, MammalianHumansInhibitor of Apoptosis ProteinsIntracellular Signaling Peptides and ProteinsJC VirusMiceMice, KnockoutMicrotubule-Associated ProteinsNeuronsProtein Serine-Threonine KinasesAntigens, Polyomavirus TransformingBirc5 protein, mouseInhibitor of Apoptosis ProteinsIntracellular Signaling Peptides and ProteinsMicrotubule-Associated ProteinsMTOR protein, humanmTOR protein, mouseProtein Serine-Threonine KinasesReceptor, IGF Type 1Repressor ProteinsRNA, Small InterferingSurvivinTOR Serine-Threonine Kinases

Identifiers

PMID19834489
PMCPMC2822053
OpenAlexW2041163560

What OpenQuestion holds

Textmetadata
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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.