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TSPAN8 promotes cancer cell stemness via activation of sonic Hedgehog signaling

Cancer stem cells (CSCs) represent a major source of treatment resistance and tumor progression. However, regulation of CSCs stemness is not entirely understood. Here, we report that TSPAN8 expression is upregulated in breast CSCs, promotes the expression of the stemness gene NANOG, OCT4, and ALDHA1...

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Autores principales: Zhu, Rongxuan, Gires, Olivier, Zhu, Liqun, Liu, Jun, Li, Junjian, Yang, Hao, Ju, Gaoda, Huang, Jing, Ge, Weiyu, Chen, Yi, Lu, Zhimin, Wang, Hongxia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6599078/
https://www.ncbi.nlm.nih.gov/pubmed/31253779
http://dx.doi.org/10.1038/s41467-019-10739-3
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author Zhu, Rongxuan
Gires, Olivier
Zhu, Liqun
Liu, Jun
Li, Junjian
Yang, Hao
Ju, Gaoda
Huang, Jing
Ge, Weiyu
Chen, Yi
Lu, Zhimin
Wang, Hongxia
author_facet Zhu, Rongxuan
Gires, Olivier
Zhu, Liqun
Liu, Jun
Li, Junjian
Yang, Hao
Ju, Gaoda
Huang, Jing
Ge, Weiyu
Chen, Yi
Lu, Zhimin
Wang, Hongxia
author_sort Zhu, Rongxuan
collection PubMed
description Cancer stem cells (CSCs) represent a major source of treatment resistance and tumor progression. However, regulation of CSCs stemness is not entirely understood. Here, we report that TSPAN8 expression is upregulated in breast CSCs, promotes the expression of the stemness gene NANOG, OCT4, and ALDHA1, and correlates with therapeutic resistance. Mechanistically, TSPAN8 interacts with PTCH1 and inhibits the degradation of the SHH/PTCH1 complex through recruitment of deubiquitinating enzyme ATXN3. This results in the translocation of SMO to cilia, downstream gene expression, resistance of CSCs to chemotherapeutic agents, and enhances tumor formation in mice. Accordingly, expression levels of TSPAN8, PTCH1, SHH, and ATXN3 are positively correlated in human breast cancer specimens, and high TSPAN8 and ATXN3 expression levels correlate with poor prognosis. These findings reveal a molecular basis of TSPAN8-enhanced Sonic Hedgehog signaling and highlight a role for TSPAN8 in promoting cancer stemness.
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spelling pubmed-65990782019-07-01 TSPAN8 promotes cancer cell stemness via activation of sonic Hedgehog signaling Zhu, Rongxuan Gires, Olivier Zhu, Liqun Liu, Jun Li, Junjian Yang, Hao Ju, Gaoda Huang, Jing Ge, Weiyu Chen, Yi Lu, Zhimin Wang, Hongxia Nat Commun Article Cancer stem cells (CSCs) represent a major source of treatment resistance and tumor progression. However, regulation of CSCs stemness is not entirely understood. Here, we report that TSPAN8 expression is upregulated in breast CSCs, promotes the expression of the stemness gene NANOG, OCT4, and ALDHA1, and correlates with therapeutic resistance. Mechanistically, TSPAN8 interacts with PTCH1 and inhibits the degradation of the SHH/PTCH1 complex through recruitment of deubiquitinating enzyme ATXN3. This results in the translocation of SMO to cilia, downstream gene expression, resistance of CSCs to chemotherapeutic agents, and enhances tumor formation in mice. Accordingly, expression levels of TSPAN8, PTCH1, SHH, and ATXN3 are positively correlated in human breast cancer specimens, and high TSPAN8 and ATXN3 expression levels correlate with poor prognosis. These findings reveal a molecular basis of TSPAN8-enhanced Sonic Hedgehog signaling and highlight a role for TSPAN8 in promoting cancer stemness. Nature Publishing Group UK 2019-06-28 /pmc/articles/PMC6599078/ /pubmed/31253779 http://dx.doi.org/10.1038/s41467-019-10739-3 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zhu, Rongxuan
Gires, Olivier
Zhu, Liqun
Liu, Jun
Li, Junjian
Yang, Hao
Ju, Gaoda
Huang, Jing
Ge, Weiyu
Chen, Yi
Lu, Zhimin
Wang, Hongxia
TSPAN8 promotes cancer cell stemness via activation of sonic Hedgehog signaling
title TSPAN8 promotes cancer cell stemness via activation of sonic Hedgehog signaling
title_full TSPAN8 promotes cancer cell stemness via activation of sonic Hedgehog signaling
title_fullStr TSPAN8 promotes cancer cell stemness via activation of sonic Hedgehog signaling
title_full_unstemmed TSPAN8 promotes cancer cell stemness via activation of sonic Hedgehog signaling
title_short TSPAN8 promotes cancer cell stemness via activation of sonic Hedgehog signaling
title_sort tspan8 promotes cancer cell stemness via activation of sonic hedgehog signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6599078/
https://www.ncbi.nlm.nih.gov/pubmed/31253779
http://dx.doi.org/10.1038/s41467-019-10739-3
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