Evidence map›Paper›PMID 12420220›Full record

ArticleOncogene2002

Lung-specific expression of human mutant p53-273H is associated with a high frequency of lung adenocarcinoma in transgenic mice.

Wenrui Duan, Haiming Ding, Mark A Subler, Wei-Guo Zhu, Huiming Zhang, Gary D Stoner, Jolene J Windle, Gregory A Otterson, Miguel A Villalona-Calero

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

13 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Mutant p53 in cancer therapy-the barrier or the path.Journal of molecular cell biology · 2019
    Review
  4. Review
  5. Article
  6. OncomorphicJournal of cancer therapy · 2014
    Article
  7. Mutant p53 gain-of-function in cancer.Cold Spring Harbor perspectives in biology · 2010
    Review
  8. Review
  9. Article
  10. A mouse model for EML4-ALK-positive lung cancer.Proceedings of the National Academy of Sciences of the United States of America · 2008
    Article
  11. Article
  12. Article
  13. Cancer stem cells: the lessons from pre-cancerous stem cells.Journal of cellular and molecular medicine
    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

9 authors at 3 institutions in 1 country.

Wenrui DuanComprehensive Cancer Center, The Ohio State University College of Medicine and Public Health, Columbus, Ohio, OH 43210, USA.
Haiming Ding
Mark A Subler
Wei-Guo Zhu
Huiming Zhang
Gary D Stoner
Jolene J Windle
Gregory A Otterson
Miguel A Villalona-Calero
The Ohio State University · USVirginia Commonwealth University · USOhio Department of Health · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
TRANSLATIONAL RESEARCH IN LUNG CANCERK01CA076970 · NCI · OHIO STATE UNIVERSITY · PI VILLALONA, MIGUEL ANGEL · 1997 to 2002
$484k
NCI NIH HHS K01 CA76970NCI NIH HHS P30 CA16058
6 · The paper itself

Abstract

To investigate the tumorigenic potential of mutant p53 when selectively expressed in lung tissue, a transgenic mouse model was developed in which a mutant form of p53 (p53-273H) was placed under the transcriptional control of the lung-specific human surfactant protein C (SP-C) promoter. Two founder mice were identified, and a line of SP-C/p53-273H transgenic mice was established from one of the founders. Human p53-273H protein was detected specifically in lung tissue from transgenic mice. Malignant tumors, which were histologically characterized as adenocarcinomas, were observed in transgenic mice, with the earliest onset documented at 4 months of age. To further evaluate incidence and onset of tumor formation, transgenic mice (n=113) were sacrificed at age intervals ranging from 4-15 months. At 13-15 months of age, transgenic mice were significantly more likely to have lung tumors at necropsy than age-matched non-transgenic littermates (9 out of 39 (23%) versus 2 out of 35 (5.7%), chi(2) test, P=0.036). The SP-C/p53-273H transgenic mice described here thus represent a genetically defined model with which to study the role of p53 mutations in lung tumorigenesis, as well as the potential complementary contributions of other genetic alterations or environmental carcinogens to lung tumor development.

Indexed as

Amino Acid SubstitutionGenes, p53Mutation, MissensePoint MutationAdenocarcinomaAge of OnsetAnimalsCell Transformation, NeoplasticFemaleGene Expression ProfilingHumansLungLung NeoplasmsMaleMiceMice, TransgenicPulmonary Surfactant-Associated Protein CRecombinant Fusion ProteinsRNA, MessengerTumor Suppressor Protein p53

Identifiers

PMID12420220
OpenAlexW2006114353

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.