Evidence map›Paper›PMID 19448672›Full record

ArticleOncogene2009

Ror2, a developmentally regulated kinase, promotes tumor growth potential in renal cell carcinoma.

T M Wright, A R Brannon, J D Gordan, A J Mikels, C Mitchell, S Chen, I Espinosa, M van de Rijn, R Pruthi, E Wallen and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Oncogene, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

63 citing papers in PubMed, 111 citations in OpenAlex.

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3 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.

T M WrightCurriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7295, USA.
A R Brannon
J D Gordan
A J Mikels
C Mitchell
S Chen
I Espinosa
M van de Rijn
R Pruthi
E Wallen
L Edwards
R Nusse
W K Rathmell
University of North Carolina at Chapel Hill · USHoward Hughes Medical Institute · USStanford University · USUniversity of Pennsylvania · US

Funding

UNC Initiative for Maximizing Student DevelopmentR25GM055336 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI COOK, JEANETTE GOWEN, KASH, THOMAS L. · 1996 to 2023
$12.1M
Functional and Tissue Specific Effects of VHL MutationsK08CA098410 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RATHMELL, WENDY K · 2003 to 2007
$668k
Analysis of the Novel Kinase ROR2: A New Molecular Target in Renal Cell CarcinomaF31CA132543 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WRIGHT, TRICIA M · 2007 to 2010
$73k
NCI NIH HHS F31 CA132543NCI NIH HHS F31CA132543NCI NIH HHS K08 CA098410NIGMS NIH HHS R25 GM055336NIGMS NIH HHS R25GM055336
6 · The paper itself

Abstract

Inappropriate kinase expression and subsequent promiscuous activity defines the transformation of many solid tumors including renal cell carcinoma (RCC). Thus, the expression of novel tumor-associated kinases has the potential to dramatically shape tumor cell behavior. Further, identifying tumor-associated kinases can lend insight into patterns of tumor growth and characteristics. Here, we report the identification of the RTK-like orphan receptor 2 (Ror2), a new tumor-associated kinase in RCC cell lines and primary tumors. Ror2 is an orphan receptor tyrosine kinase with physiological expression normally seen in the embryonic kidney. However, in RCC, Ror2 expression correlated with expression of genes involved at the extracellular matrix, including Twist and matrix metalloprotease-2 (MMP2). Expression of MMP2 in RCC cells was suppressed by Ror2 knockdown, placing Ror2 as a mediator of MMP2 regulation in RCC and a potential regulator of extracellular matrix remodeling. The suppression of Ror2 not only inhibited cell migration, but also inhibited anchorage-independent growth in soft agar and growth in an orthotopic xenograft model. These findings suggest a novel pathway of tumor-promoting activity by Ror2 within a subset of renal carcinomas, with significant implications for unraveling the tumorigenesis of RCC.

Indexed as

Cell ProliferationAnimalsCarcinoma, Renal CellCell Line, TumorCell MovementGene Expression ProfilingGene Expression Regulation, NeoplasticHumansImmunoblottingImmunohistochemistryKidney NeoplasmsMatrix Metalloproteinase 2MiceMice, NudeNeoplasms, ExperimentalNeoplasm TransplantationMatrix Metalloproteinase 2Nuclear ProteinsReceptor Protein-Tyrosine KinasesReceptors, Cell SurfaceReceptor Tyrosine Kinase-like Orphan ReceptorsROR2 protein, humanTWIST1 protein, humanTwist-Related Protein 1

Identifiers

PMID19448672
PMCPMC2771692
OpenAlexW2080193153

What OpenQuestion holds

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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.