Evidence map›Paper›PMID 17661719›Full record

ReviewFuture oncology (London, England)2007

Ron-receptor tyrosine kinase in tumorigenesis and metastasis.

Mike A Leonis, Megan N Thobe, Susan E Waltz

Abstract readReview
In one paragraph

Review in Future oncology (London, England), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.0field-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

23 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
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  15. Article
  16. Ron receptor-dependent gene regulation in a mouse model of endotoxin-induced acute liver failure.Hepatobiliary & pancreatic diseases international : HBPD INT · 2012
    Article
  17. Article
  18. Article
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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

3 authors at 1 institution in 1 country.

Mike A LeonisUniversity of Cincinnati College of Medicine, Department of Pediatrics, Cincinnati, OH 45267-0558, USA.
Megan N Thobe
Susan E Waltz
University of Cincinnati Medical Center · US

Funding

Cincinnati DDRDC: Center for Growth and Development (CGDR24DK064403 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI COHEN, MITCHELL B · 2003 to 2006
$2.1M
Hepatocyte Growth Factor-like Protein ReceptorR01DK073552 · NIDDK · UNIVERSITY OF CINCINNATI · PI WALTZ, SUSAN E · 2005 to 2009
$1.5M
The Ron Receptor in Mammary Gland BiologyR01CA100002 · NCI · UNIVERSITY OF CINCINNATI · PI WALTZ, SUSAN E · 2004 to 2008
$1.5M
The Ron Receptor/Chemokine Axis in Prostate CancerR01CA125379 · NCI · UNIVERSITY OF CINCINNATI · PI WALTZ, SUSAN E · 2008 to 2012
$1.3M
The Ron Receptor Tyrosine Kinase in Hepatic TumorigenesisK08CA111819 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI LEONIS, MIKE A · 2006 to 2010
$664k
NCI NIH HHS CA-100002NCI NIH HHS CA-111819NCI NIH HHS K08 CA111819NCI NIH HHS R01 CA100002NCI NIH HHS R01 CA125379NIDDK NIH HHS DK-064403NIDDK NIH HHS DK-073552NIDDK NIH HHS R01 DK073552NIDDK NIH HHS R24 DK064403
6 · The paper itself

Abstract

The Ron-receptor tyrosine kinase has been increasingly recognized for its tumorigenic potential in the last decade. Ron-receptor activation leads to the activation of common receptor tyrosine kinase downstream-signaling pathways, and most prominently in tumor models, activation of MAPK, PI3K and beta-catenin. Numerous experimental models of mammalian tumorigenesis have demonstrated that increased Ron-receptor activity correlates with increased tumorigenesis in a variety of organs of epithelial origin. The evidence for Ron as an oncogene in human tumor biology is growing. The Ron receptor is overexpressed and over activated in a large number of human tumors, and overexpression of Ron correlates with a worse clinical outcome for patients in at least two human cancer states, namely breast and bladder cancer. Several experimental approaches have been demonstrated to successfully block Ron activity and function, and given these convincing data, approaches to block Ron-receptor activity in targeted human cancers should prove to be fruitful in the setting of future clinical research trials.

Indexed as

AnimalsCell Transformation, NeoplasticHepatocyte Growth FactorHumansMiceNeoplasm MetastasisOncogenesProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesHepatocyte Growth Factormacrophage stimulating proteinProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesRON protein

Identifiers

PMID17661719
PMCPMC4082960
OpenAlexW2089121621

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.