Evidence map›Paper›PMID 11175352›Full record

ArticleOncogene2000

Specific pattern of p53 phosphorylation during nitric oxide-induced cell cycle arrest.

N Nakaya, S W Lowe, Y Taya, A Chenchik, G Enikolopov

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
  2. Article
  3. M1 macrophage dependent-p53 regulates the intracellular survival of mycobacteria.Apoptosis : an international journal on programmed cell death · 2020
    Article
  4. Article
  5. Review
  6. Trp53 deficiency protects against acute intestinal inflammation.Journal of immunology (Baltimore, Md. : 1950) · 2013
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Nitric oxide is a physiological inhibitor of neurogenesis in the adult mouse subventricular zone and olfactory bulb.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2004
    Article
  12. Article
  13. Review
  14. Nitric oxide-induced cellular stress and p53 activation in chronic inflammation.Proceedings of the National Academy of Sciences of the United States of America · 2003
    Article
  15. 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

5 authors at 3 institutions in 2 countries.

N NakayaCold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
S W Lowe
Y Taya
A Chenchik
G Enikolopov
Cold Spring Harbor Laboratory · USNational Cancer Research Institute · GBTakara (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nitric oxide (NO) is an efficient inhibitor of cell proliferation. Here we show that part of the antiproliferative activity of NO in fibroblasts is mediated through p53 signaling pathway. Cells from p53-/- knockout mice are compromised in their ability to stop dividing in the presence of NO. NO strongly induces expression of genes which are transcriptional targets of p53, and p53 is necessary for some, but not all, of the transcription activation effects of NO. Furthermore, NO strongly increases the cellular level of p53 protein. Since phosphorylation of particular residues of the p53 molecule has been correlated with its functional activity, we determined the phosphorylation pattern of p53 molecule after exposure to NO and compared it with the phosphorylation patterns that develop upon treatment with gamma-irradiation, UV light, and adriamycin. We found that NO induces a specific signature pattern of p53 phosphorylation, distinct from the patterns evoked by other inducers. This study suggests that NO activates specific signaling pathways that may partially overlap, but that do not coincide, with signaling pathways activated by other known inducers of p53 activity.

Indexed as

Gene Expression Profiling3T3 CellsAnimalsCell CycleCell DivisionDoxorubicinFibroblastsGamma RaysMiceMice, KnockoutNitric OxidePhosphorylationSignal TransductionTranscriptional ActivationTumor Suppressor Protein p53Ultraviolet RaysDoxorubicinNitric OxideTumor Suppressor Protein p53

Identifiers

PMID11175352
OpenAlexW1992981111

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.