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

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-ass...

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Autores principales: Wright, Tricia M, Brannon, A Rose, Gordan, John D, Mikels, Amanda J, Mitchell, Cicely, Chen, Shufen, Espinosa, Inigo, van de Rijn, Matt, Pruthi, Raj, Wallen, Eric, Edwards, Lloyd, Nusse, Roel, Rathmell, W Kimryn
Formato: Texto
Lenguaje:English
Publicado: 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2771692/
https://www.ncbi.nlm.nih.gov/pubmed/19448672
http://dx.doi.org/10.1038/onc.2009.116
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author Wright, Tricia M
Brannon, A Rose
Gordan, John D
Mikels, Amanda J
Mitchell, Cicely
Chen, Shufen
Espinosa, Inigo
van de Rijn, Matt
Pruthi, Raj
Wallen, Eric
Edwards, Lloyd
Nusse, Roel
Rathmell, W Kimryn
author_facet Wright, Tricia M
Brannon, A Rose
Gordan, John D
Mikels, Amanda J
Mitchell, Cicely
Chen, Shufen
Espinosa, Inigo
van de Rijn, Matt
Pruthi, Raj
Wallen, Eric
Edwards, Lloyd
Nusse, Roel
Rathmell, W Kimryn
author_sort Wright, Tricia M
collection PubMed
description 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 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.
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spelling pubmed-27716922010-01-09 Ror2, a developmentally regulated kinase, promotes tumor growth potential in renal cell carcinoma Wright, Tricia M Brannon, A Rose Gordan, John D Mikels, Amanda J Mitchell, Cicely Chen, Shufen Espinosa, Inigo van de Rijn, Matt Pruthi, Raj Wallen, Eric Edwards, Lloyd Nusse, Roel Rathmell, W Kimryn Oncogene Article 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 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. 2009-05-18 2009-07-09 /pmc/articles/PMC2771692/ /pubmed/19448672 http://dx.doi.org/10.1038/onc.2009.116 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Wright, Tricia M
Brannon, A Rose
Gordan, John D
Mikels, Amanda J
Mitchell, Cicely
Chen, Shufen
Espinosa, Inigo
van de Rijn, Matt
Pruthi, Raj
Wallen, Eric
Edwards, Lloyd
Nusse, Roel
Rathmell, W Kimryn
Ror2, a developmentally regulated kinase, promotes tumor growth potential in renal cell carcinoma
title Ror2, a developmentally regulated kinase, promotes tumor growth potential in renal cell carcinoma
title_full Ror2, a developmentally regulated kinase, promotes tumor growth potential in renal cell carcinoma
title_fullStr Ror2, a developmentally regulated kinase, promotes tumor growth potential in renal cell carcinoma
title_full_unstemmed Ror2, a developmentally regulated kinase, promotes tumor growth potential in renal cell carcinoma
title_short Ror2, a developmentally regulated kinase, promotes tumor growth potential in renal cell carcinoma
title_sort ror2, a developmentally regulated kinase, promotes tumor growth potential in renal cell carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2771692/
https://www.ncbi.nlm.nih.gov/pubmed/19448672
http://dx.doi.org/10.1038/onc.2009.116
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