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INTU is essential for oncogenic Hh signaling through regulating primary cilia formation in basal cell carcinoma (BCC)

Inturned (INTU), a cilia and planar polarity effector (CPLANE), performs prominent ciliogenic functions during morphogenesis, such as in the skin. INTU is expressed in adult tissues but its role in tissue maintenance is unknown. Here, we report that the expression of the INTU gene is aberrantly elev...

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Autores principales: Yang, Ning, Leung, Elaine Lai-Han, Liu, Chengbao, Li, Li, Eguether, Thibaut, Yao, Xiao Jun, Jones, Evan C., Norris, David A., Liu, Aimin, Clark, Richard A., Roop, Dennis R., Pazour, Gregory J., Shroyer, Kenneth R., Chen, Jiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578876/
https://www.ncbi.nlm.nih.gov/pubmed/28459465
http://dx.doi.org/10.1038/onc.2017.117
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author Yang, Ning
Leung, Elaine Lai-Han
Liu, Chengbao
Li, Li
Eguether, Thibaut
Yao, Xiao Jun
Jones, Evan C.
Norris, David A.
Liu, Aimin
Clark, Richard A.
Roop, Dennis R.
Pazour, Gregory J.
Shroyer, Kenneth R.
Chen, Jiang
author_facet Yang, Ning
Leung, Elaine Lai-Han
Liu, Chengbao
Li, Li
Eguether, Thibaut
Yao, Xiao Jun
Jones, Evan C.
Norris, David A.
Liu, Aimin
Clark, Richard A.
Roop, Dennis R.
Pazour, Gregory J.
Shroyer, Kenneth R.
Chen, Jiang
author_sort Yang, Ning
collection PubMed
description Inturned (INTU), a cilia and planar polarity effector (CPLANE), performs prominent ciliogenic functions during morphogenesis, such as in the skin. INTU is expressed in adult tissues but its role in tissue maintenance is unknown. Here, we report that the expression of the INTU gene is aberrantly elevated in human basal cell carcinoma (BCC), coinciding with increased primary cilia formation and activated hedgehog (Hh) signaling. Disrupting Intu in an oncogenic mutant Smo (SmoM2)-driven BCC mouse model prevented the formation of BCC through suppressing primary cilia formation and Hh signaling, suggesting that Intu performs a permissive role during BCC formation. INTU is essential for IFT-A complex assembly during ciliogenesis. To further determine whether Intu is directly involved in the activation of Hh signaling downstream of ciliogenesis, we examined the Hh signaling pathway in mouse embryonic fibroblasts, which readily respond to Hh pathway activation. Depleting Intu blocked SAG-induced Hh pathway activation, whereas the expression of Gli2ΔN, a constitutively active Gli2, restored Hh pathway activation in Intu-deficient cells, suggesting that INTU functions upstream of Gli2 activation. In contrast, overexpressing Intu did not promote ciliogenesis or Hh signaling. Taken together, data obtained from this study suggest that INTU is indispensable during BCC tumorigenesis and that its aberrant upregulation is likely a prerequisite for primary cilia formation during Hh-dependent tumorigenesis.
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spelling pubmed-55788762017-11-01 INTU is essential for oncogenic Hh signaling through regulating primary cilia formation in basal cell carcinoma (BCC) Yang, Ning Leung, Elaine Lai-Han Liu, Chengbao Li, Li Eguether, Thibaut Yao, Xiao Jun Jones, Evan C. Norris, David A. Liu, Aimin Clark, Richard A. Roop, Dennis R. Pazour, Gregory J. Shroyer, Kenneth R. Chen, Jiang Oncogene Article Inturned (INTU), a cilia and planar polarity effector (CPLANE), performs prominent ciliogenic functions during morphogenesis, such as in the skin. INTU is expressed in adult tissues but its role in tissue maintenance is unknown. Here, we report that the expression of the INTU gene is aberrantly elevated in human basal cell carcinoma (BCC), coinciding with increased primary cilia formation and activated hedgehog (Hh) signaling. Disrupting Intu in an oncogenic mutant Smo (SmoM2)-driven BCC mouse model prevented the formation of BCC through suppressing primary cilia formation and Hh signaling, suggesting that Intu performs a permissive role during BCC formation. INTU is essential for IFT-A complex assembly during ciliogenesis. To further determine whether Intu is directly involved in the activation of Hh signaling downstream of ciliogenesis, we examined the Hh signaling pathway in mouse embryonic fibroblasts, which readily respond to Hh pathway activation. Depleting Intu blocked SAG-induced Hh pathway activation, whereas the expression of Gli2ΔN, a constitutively active Gli2, restored Hh pathway activation in Intu-deficient cells, suggesting that INTU functions upstream of Gli2 activation. In contrast, overexpressing Intu did not promote ciliogenesis or Hh signaling. Taken together, data obtained from this study suggest that INTU is indispensable during BCC tumorigenesis and that its aberrant upregulation is likely a prerequisite for primary cilia formation during Hh-dependent tumorigenesis. 2017-05-01 2017-08-31 /pmc/articles/PMC5578876/ /pubmed/28459465 http://dx.doi.org/10.1038/onc.2017.117 Text en 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
Yang, Ning
Leung, Elaine Lai-Han
Liu, Chengbao
Li, Li
Eguether, Thibaut
Yao, Xiao Jun
Jones, Evan C.
Norris, David A.
Liu, Aimin
Clark, Richard A.
Roop, Dennis R.
Pazour, Gregory J.
Shroyer, Kenneth R.
Chen, Jiang
INTU is essential for oncogenic Hh signaling through regulating primary cilia formation in basal cell carcinoma (BCC)
title INTU is essential for oncogenic Hh signaling through regulating primary cilia formation in basal cell carcinoma (BCC)
title_full INTU is essential for oncogenic Hh signaling through regulating primary cilia formation in basal cell carcinoma (BCC)
title_fullStr INTU is essential for oncogenic Hh signaling through regulating primary cilia formation in basal cell carcinoma (BCC)
title_full_unstemmed INTU is essential for oncogenic Hh signaling through regulating primary cilia formation in basal cell carcinoma (BCC)
title_short INTU is essential for oncogenic Hh signaling through regulating primary cilia formation in basal cell carcinoma (BCC)
title_sort intu is essential for oncogenic hh signaling through regulating primary cilia formation in basal cell carcinoma (bcc)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578876/
https://www.ncbi.nlm.nih.gov/pubmed/28459465
http://dx.doi.org/10.1038/onc.2017.117
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