Evidence map›Paper›PMID 8922388›Full record

ArticleThe Journal of cell biology1996

Adenovirus-mediated gene transfer of the tumor suppressor, p53, induces apoptosis in postmitotic neurons.

R S Slack, D J Belliveau, M Rosenberg, J Atwal, H Lochmüller, R Aloyz, A Haghighi, B Lach, P Seth, E Cooper and 1 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of cell biology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
7.0field-weighted citation impact, top 3% 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

46 citing papers in PubMed, 124 citations in OpenAlex.

  1. Article
  2. ProapoptoticInternational journal of molecular sciences · 2021
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. DAPK1-p53 interaction converges necrotic and apoptotic pathways of ischemic neuronal death.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  8. Article
  9. UBE4B: a promising regulatory molecule in neuronal death and survival.International journal of molecular sciences · 2012
    Review
  10. Article
  11. Article
  12. Article
  13. p63 antagonizes p53 to promote the survival of embryonic neural precursor cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2009
    Article
  14. Necdin regulates p53 acetylation via Sirtuin1 to modulate DNA damage response in cortical neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2008
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. p53 activation domain 1 is essential for PUMA upregulation and p53-mediated neuronal cell death.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2004
    Article
  20. Evidence that DeltaNp73 promotes neuronal survival by p53-dependent and p53-independent mechanisms.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2004
    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

11 authors at 1 institution in 1 country.

R S SlackCentre for Neuronal Survival, Montreal Neurological Institute, McGill University, Canada.
D J Belliveau
M Rosenberg
J Atwal
H Lochmüller
R Aloyz
A Haghighi
B Lach
P Seth
E Cooper
F D Miller
Montreal Neurological Institute and Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Programmed cell death is an ongoing process in both the developing and the mature nervous system. The tumor suppressor gene, p53, can induce apoptosis in a number of different cell types. Recently, the enhanced expression of p53 has been observed during acute neurological disease. To determine whether p53 overexpression could influence neuronal survival, we used a recombinant adenovirus vector carrying wild type p53 to transduce postmitotic neurons. A control consisting of the same adenovirus vector background but carrying the lacZ reporter expression cassette was used to establish working parameters for the effective genetic manipulation of sympathetic neurons. We have found that recombinant adenovirus can be used at titers sufficiently high (10 to 50 multiplicity of infection) to transduce the majority of the neuronal population without perturbing survival, electrophysiological function, or cytoarchitecture. Moreover, we demonstrate that overexpression of wild type p53 is sufficient to induce programmed cell death in neurons. The observation that p53 is capable of inducing apoptosis in postmitotic neurons has major implications for the mechanisms of cell death in the traumatized mature nervous system.

Indexed as

AdenoviridaeGene Transfer TechniquesAnimalsApoptosisBiotinCell SurvivalCellular SenescenceDeoxyuracil NucleotidesDNA FragmentationElectrophysiologyGene ExpressionMicroscopy, ElectronMitosisNeuronsRatsRats, Sprague-DawleyBiotinDeoxyuracil NucleotidesRecombinant ProteinsTumor Suppressor Protein p53

Identifiers

PMID8922388
PMCPMC2133379
OpenAlexW2153494843

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.