Evidence map›Paper›PMID 12214279›Full record

ArticleOncogene2002

Targeted expression of the receptor tyrosine kinase RON in distal lung epithelial cells results in multiple tumor formation: oncogenic potential of RON in vivo.

Yi-Qing Chen, Yong-Qing Zhou, James H Fisher, Ming-Hai Wang

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 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Ron-receptor tyrosine kinase in tumorigenesis and metastasis.Future oncology (London, England) · 2007
    Review
  13. Article
  14. Coordinate expression and functional profiling identify an extracellular proteolytic signaling pathway.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Article
  15. Article
  16. Article
  17. Article
  18. 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

4 authors at 3 institutions in 2 countries.

Yi-Qing ChenDivision of Pulmonary Sciences and Critical Care, Department of Medicine, University of Colorado School of Medicine, CU Cancer Center, and Denver Health Medical Center, Denver, Colorado, CO 80204, USA.
Yong-Qing Zhou
James H Fisher
Ming-Hai Wang
Denver Health Medical Center · USFirst Affiliated Hospital Zhejiang University · CNUniversity of Colorado Denver · US

Funding

The RON Receptor in the Invasive Growth of Colon CancersR01CA091980 · NCI · UNIVERSITY OF COLORADO DENVER · PI WANG, MING-HAI · 2002 to 2012
$2.4M
REGULATION OF MACROPHAGE INOS EXPRESSIONR01AI043516 · NIAID · WAYNE STATE UNIVERSITY · PI WANG, MING-HAI · 1998 to 2001
$428k
NCI NIH HHS CA91980NIAID NIH HHS R01 AI43516
6 · The paper itself

Abstract

RON, a member of the MET proto-oncogene family, has been implicated in the progression of certain epithelial cancers. The purpose of this study was to determine the oncogenic potential of RON in vivo in lung epithelial cells. Transgenic mice were established using surfactant protein C promoter to express human RON in the distal lung epithelial cells. These mice were born normal but developed multiple lung tumors with distinct morphology and growth patterns. Tumors appeared as a single mass in the lung around 2 months of age and gradually developed into multiple nodules located mostly in the peripheral portions of the lung. A transition from early adenomas to later adenocarcinomas was observed. Morphologically, tumors were characterized as cuboidal epithelial cells with a type II cell phenotype, grew along the alveolar walls, and projected into the alveolar septa. RON was highly expressed and constitutively activated in tumors. These results indicate that overexpression of human wild-type RON causes the formation of lung tumors with unique biological characteristics in vivo. This model provides opportunities to study the role of RON in the pathogenesis of lung tumors and to elucidate the mechanisms underlying this distinct lung tumor.

Indexed as

AnimalsCell Transformation, NeoplasticGene Expression Regulation, NeoplasticHumansImmunohistochemistryLung NeoplasmsMiceMice, TransgenicProto-Oncogene MasProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesReceptors, Cell SurfaceTransgenesMAS1 protein, humanProto-Oncogene MasProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesReceptors, Cell SurfaceRON protein

Identifiers

PMID12214279
OpenAlexW2021347994

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.