Evidence map›Paper›PMID 10097112›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1999

Regulation of p53 expression by thymidylate synthase.

J Ju, J Pedersen-Lane, F Maley, E Chu

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

45 citing papers in PubMed, 120 citations in OpenAlex.

  1. Article
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  5. Detection of a G-Quadruplex as a Regulatory Element inInternational journal of molecular sciences · 2020
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  15. Article
  16. Prognostic significance of miR-215 in colon cancer.Clinical colorectal cancer · 2011
    Article
  17. Protein-protein interface-binding peptides inhibit the cancer therapy target human thymidylate synthase.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  18. Article
  19. Article
  20. Review
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

4 authors at 2 institutions in 1 country.

J JuDepartment of Medicine and Pharmacology, Yale Cancer Center, Yale University School of Medicine and VA Connecticut Healthcare System, New Haven, CT 06520, USA.
J Pedersen-Lane
F Maley
E Chu
VA Connecticut Healthcare System · USWadsworth Center · US

Funding

Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI MARCUS W BOSENBERG · 1985 to 2026
$85.0M
MOLECULAR BASIS FOR TS TRANSLATIONAL REGULATIONR01CA075712 · NCI · YALE UNIVERSITY · PI CHU, EDWARD · 1997 to 2005
$1.2M
NCI OUTSTANDING INVESTIGATORS GRANTR35CA044355 · NCI · WADSWORTH CENTER · PI MALEY, FRANK · 1987 to 2000
$164k
NCI NIH HHS CA16359NCI NIH HHS CA44355NCI NIH HHS CA75712NCI NIH HHS P30 CA016359NCI NIH HHS R01 CA075712
6 · The paper itself

Abstract

Previous studies showed that thymidylate synthase (TS), as an RNA binding protein, regulates its own synthesis by impairing the translation of TS mRNA. In this report, we present evidence that p53 expression is affected in a similar manner by TS. For these studies, we used a TS-depleted human colon cancer HCT-C cell that had been transfected with either the human TS cDNA or the Escherichia coli TS gene. The level of p53 protein in transfected cells overexpressing human TS was significantly reduced when compared with its corresponding parent HCT-C cells. This suppression of p53 expression was the direct result of decreased translational efficiency of p53 mRNA. Similar results were obtained upon transfection of HCT-C cells with pcDNA 3.1 (+) containing the E. coli TS gene. These findings provide evidence that TS, from diverse species, specifically regulates p53 expression at the translational level. In addition, TS-overexpressing cells with suppressed levels of p53 are significantly impaired in their ability to arrest in G1 phase in response to exposure to a DNA-damaging agent such as gamma-irradiation. These studies provide support for the in vivo biological relevance of the interaction between TS and p53 mRNA and identify a molecular pathway for controlling p53 expression.

Indexed as

Gene Expression Regulation, NeoplasticGenes, p53Cell CycleColonic NeoplasmsEscherichia coliG1 PhaseGamma RaysHumansProtein BiosynthesisRecombinant ProteinsReverse Transcriptase Polymerase Chain ReactionRNA, MessengerS PhaseThymidylate SynthaseTransfectionTumor Cells, CulturedRecombinant ProteinsRNA, MessengerThymidylate SynthaseTumor Suppressor Protein p53

Identifiers

PMID10097112
PMCPMC22369
OpenAlexW2022162825

What OpenQuestion holds

Texttitle and abstract
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.