Evidence map›Paper›PMID 16107692›Full record

ArticleMolecular and cellular biology2005

Role of Stat3 in regulating p53 expression and function.

Guilian Niu, Kenneth L Wright, Yihong Ma, Gabriela M Wright, Mei Huang, Rosalyn Irby, Jon Briggs, James Karras, W Douglas Cress, Drew Pardoll and 3 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 205 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
205citing papers in PubMed, 1 pooled it
5.7field-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

205 citing papers in PubMed, 1 synthesis or guideline pooled it, 396 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Cellular signaling meets bacterial infection: the integrative role of STAT3.Frontiers in cellular and infection microbiology · 2026
    Review
  4. Article
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  11. Review
  12. Elucidation ofFrontiers in pharmacology · 2025
    Article
  13. Article
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  16. Review
  17. Article
  18. Article
  19. Review
  20. Unraveling the complexity of STAT3 in cancer: molecular understanding and drug discovery.Journal of experimental & clinical cancer research : CR · 2024
    Review

145 more citing papers are in PubMed but not listed here.

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

13 authors at 4 institutions in 1 country.

Guilian NiuImmunology Program, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.
Kenneth L Wright
Yihong Ma
Gabriela M Wright
Mei Huang
Rosalyn Irby
Jon Briggs
James Karras
W Douglas Cress
Drew Pardoll
Richard Jove
Jiangdong Chen
Hua Yu
University of South Florida · USMolecular Oncology (United States) · USIonis Pharmaceuticals (United States) · USJohns Hopkins Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Loss of p53 function by mutation is common in cancer. However, most natural p53 mutations occur at a late stage in tumor development, and many clinically detectable cancers have reduced p53 expression but no p53 mutations. It remains to be fully determined what mechanisms disable p53 during malignant initiation and in cancers without mutations that directly affect p53. We show here that oncogenic signaling pathways inhibit the p53 gene transcription rate through a mechanism involving Stat3, which binds to the p53 promoter in vitro and in vivo. Site-specific mutation of a Stat3 DNA-binding site in the p53 promoter partially abrogates Stat3-induced inhibition. Stat3 activity also influences p53 response genes and affects UV-induced cell growth arrest in normal cells. Furthermore, blocking Stat3 in cancer cells up-regulates expression of p53, leading to p53-mediated tumor cell apoptosis. As a point of convergence for many oncogenic signaling pathways, Stat3 is constitutively activated at high frequency in a wide diversity of cancers and is a promising molecular target for cancer therapy. Thus, repression of p53 expression by Stat3 is likely to have an important role in development of tumors, and targeting Stat3 represents a novel therapeutic approach for p53 reactivation in many cancers lacking p53 mutations.

Indexed as

Gene Expression RegulationAnimalsApoptosisCell ProliferationDNA-Binding ProteinsElectrophoretic Mobility Shift AssayHumansMiceNeoplasmsPromoter Regions, GeneticResponse ElementsSignal TransductionSTAT3 Transcription FactorTrans-ActivatorsTranscription, GeneticTumor Suppressor Protein p53DNA-Binding ProteinsSTAT3 protein, humanStat3 protein, mouseSTAT3 Transcription FactorTrans-ActivatorsTumor Suppressor Protein p53

Identifiers

PMID16107692
PMCPMC1190305
OpenAlexW2114445658

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.