Evidence map›Paper›PMID 23893409›Full record

ArticleThe Journal of biological chemistry2013

Receptor tyrosine kinase-like orphan receptor 2 (Ror2) expression creates a poised state of Wnt signaling in renal cancer.

Neal R Rasmussen, Tricia M Wright, Samira A Brooks, Kathryn E Hacker, Zufan Debebe, Adam B Sendor, Matthew P Walker, Michael Ben Major, Jennifer Green, Geoffrey M Wahl and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

20 citing papers in PubMed, 25 citations in OpenAlex.

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  12. Validation of specificity of antibodies for immunohistochemistry: the case of ROR2.Virchows Archiv : an international journal of pathology · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. Ror2 as a therapeutic target in cancer.Pharmacology & therapeutics · 2015
    Review
  17. Article
  18. Article
  19. Article
  20. 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

11 authors at 3 institutions in 2 countries.

Neal R RasmussenFrom the Curriculum in Genetics and Molecular Biology,; Lineberger Comprehensive Cancer Center.
Tricia M WrightFrom the Curriculum in Genetics and Molecular Biology,; Lineberger Comprehensive Cancer Center.
Samira A BrooksLineberger Comprehensive Cancer Center,; Curriculum in Toxicology.
Kathryn E HackerFrom the Curriculum in Genetics and Molecular Biology,; Lineberger Comprehensive Cancer Center.
Zufan DebebeLineberger Comprehensive Cancer Center.
Adam B SendorLineberger Comprehensive Cancer Center.
Matthew P WalkerLineberger Comprehensive Cancer Center.
Michael Ben MajorLineberger Comprehensive Cancer Center,; Department of Cell Biology and Physiology, and.
Jennifer Greenthe Gene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, California 92037.
Geoffrey M Wahlthe Gene Expression Laboratory, Salk Institute for Biological Studies, La Jolla, California 92037.
W Kimryn RathmellLineberger Comprehensive Cancer Center,; Departments of Medicine and Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, and. Electronic address: Rathmell@med.unc.edu.
UNC Lineberger Comprehensive Cancer CenterSalk Institute for Biological Studies · USSegeberger Kliniken · DE

Funding

Integrated Training in Cancer Model SystemsT32CA009156 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DER, CHANNING J. · 1985 to 2020
$19.7M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM008719 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DARVILLE, TONI, DESHMUKH, MOHANISH P · 1999 to 2023
$15.1M
TOXICOLOGYT32ES007126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ILONA JASPERS, Bernard E. Weissman · 1985 to 2026
$13.0M
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
Pre-doctoral Training Program in Integrative Vascular BiologyT32HL069768 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Christopher P. Mack · 2002 to 2026
$9.7M
NRSA IN GENETICST32GM007092 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SEKELSKY, JEFF J. · 1985 to 2019
$5.9M
CANCER CELL BIOLOGY TRAINING PROGRAMT32CA071341 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHANNING J. DER, Yuliya Pylayeva-Gupta · 1996 to 2026
$5.0M
Genetic Events in the Development of Renal Cell CarcinomaR01CA121781 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RATHMELL, WENDY KIMRYN · 2007 to 2011
$1.4M
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
Howard Hughes Medical InstituteNCI NIH HHS F31 CA132543NCI NIH HHS F31CA132543NCI NIH HHS R01 CA121781NCI NIH HHS T32 CA009156NCI NIH HHS T32-CA009156NCI NIH HHS T32 CA071341NHLBI NIH HHS T32 HL069768NHLBI NIH HHS T32 HL069768-09NIEHS NIH HHS T32 ES007126NIGMS NIH HHS R25 GM055336NIGMS NIH HHS R25GM055336NIGMS NIH HHS T32 GM007092NIGMS NIH HHS T32 GM008719
6 · The paper itself

Abstract

Expression of the receptor tyrosine kinase-like orphan receptor 2 (Ror2) has been identified in an increasing array of tumor types and is known to play a role as an important mediator of Wnt signaling cascades. In this study, we aimed to clarify Ror2 interactions with the Wnt pathways within the context of renal cell carcinoma (RCC). An examination of Ror2 expression in primary human RCC tumors showed a significant correlation with several Wnt signaling genes, including the classical feedback target gene Axin2. We provide evidence that Ror2 expression results in a partially activated state for canonical Wnt signaling through an increased signaling pool of β-catenin, leading to an enhancement of downstream target genes following Wnt3a stimulation in both renal and renal carcinoma-derived cells. Additionally, inhibition of low-density lipoprotein receptor-related protein 6 (LRP6) with either siRNA or dickkopf decreased the response to Wnt3a stimulation, but no change was seen in the increased β-catenin pool associated with Ror2 expression, suggesting that LRP6 cofactor recruitment is necessary for a Wnt3a-induced signal but that it does not participate in the Ror2 effect on β-catenin signaling. These results highlight a new role for Ror2 in conveying a tonic signal to stabilize soluble β-catenin and create a poised state of enhanced responsiveness to Wnt3a exogenous signals in RCC.

Indexed as

Gene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticWnt Signaling PathwayAxin Proteinbeta CateninCarcinoma, Renal CellCell Line, TumorHumansKidney NeoplasmsLow Density Lipoprotein Receptor-Related Protein-6Neoplasm ProteinsReceptor Tyrosine Kinase-like Orphan ReceptorsWnt3A ProteinAXIN2 protein, humanAxin Proteinbeta CateninLow Density Lipoprotein Receptor-Related Protein-6LRP6 protein, humanNeoplasm ProteinsReceptor Tyrosine Kinase-like Orphan ReceptorsROR2 protein, humanWnt3A ProteinWNT3A protein, humanCancerRCCReceptor Tyrosine KinaseRenal Cell CarcinomaRor2SignalingWnt3aWnt Signalingβ-Catenin

Identifiers

PMID23893409
PMCPMC3764835
OpenAlexW2015880836

What OpenQuestion holds

Textmetadata
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Registered trials

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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.