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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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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. |
format | Online Article Text |
id | pubmed-5578876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
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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