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Inhibition of USP14 promotes TNFα-induced cell death in head and neck squamous cell carcinoma (HNSCC)

TNFα is a key mediator of immune, chemotherapy and radiotherapy-induced cytotoxicity, but several cancers, including head and neck squamous cell carcinomas (HNSCC), display resistance to TNFα due to activation of the canonical NFκB pro-survival pathway. However, direct targeting of this pathway is a...

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Autores principales: Morgan, Ethan L., Toni, Tiffany, Viswanathan, Ramya, Robbins, Yvette, Yang, Xinping, Cheng, Hui, Gunti, Sreenivasulu, Huynh, Angel, Sowers, Anastasia L., Mitchell, James B., Allen, Clint T., Chen, Zhong, Van Waes, Carter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154301/
https://www.ncbi.nlm.nih.gov/pubmed/37055579
http://dx.doi.org/10.1038/s41418-023-01144-x
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author Morgan, Ethan L.
Toni, Tiffany
Viswanathan, Ramya
Robbins, Yvette
Yang, Xinping
Cheng, Hui
Gunti, Sreenivasulu
Huynh, Angel
Sowers, Anastasia L.
Mitchell, James B.
Allen, Clint T.
Chen, Zhong
Van Waes, Carter
author_facet Morgan, Ethan L.
Toni, Tiffany
Viswanathan, Ramya
Robbins, Yvette
Yang, Xinping
Cheng, Hui
Gunti, Sreenivasulu
Huynh, Angel
Sowers, Anastasia L.
Mitchell, James B.
Allen, Clint T.
Chen, Zhong
Van Waes, Carter
author_sort Morgan, Ethan L.
collection PubMed
description TNFα is a key mediator of immune, chemotherapy and radiotherapy-induced cytotoxicity, but several cancers, including head and neck squamous cell carcinomas (HNSCC), display resistance to TNFα due to activation of the canonical NFκB pro-survival pathway. However, direct targeting of this pathway is associated with significant toxicity; thus, it is vital to identify novel mechanism(s) contributing to NFκB activation and TNFα resistance in cancer cells. Here, we demonstrate that the expression of proteasome-associated deubiquitinase USP14 is significantly increased in HNSCC and correlates with worse progression free survival in Human Papillomavirus (HPV)- HNSCC. Inhibition or depletion of USP14 inhibited the proliferation and survival of HNSCC cells. Further, USP14 inhibition reduced both basal and TNFα-inducible NFκB activity, NFκB-dependent gene expression and the nuclear translocation of the NFκB subunit RELA. Mechanistically, USP14 bound to both RELA and IκBα and reduced IκBα K48-ubiquitination leading to the degradation of IκBα, a critical inhibitor of the canonical NFκB pathway. Furthermore, we demonstrated that b-AP15, an inhibitor of USP14 and UCHL5, sensitized HNSCC cells to TNFα-mediated cell death, as well as radiation-induced cell death in vitro. Finally, b-AP15 delayed tumor growth and enhanced survival, both as a monotherapy and in combination with radiation, in HNSCC tumor xenograft models in vivo, which could be significantly attenuated by TNFα depletion. These data offer new insights into the activation of NFκB signaling in HNSCC and demonstrate that small molecule inhibitors targeting the ubiquitin pathway warrant further investigation as a novel therapeutic avenue to sensitize these cancers to TNFα- and radiation-induced cytotoxicity.
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spelling pubmed-101543012023-05-04 Inhibition of USP14 promotes TNFα-induced cell death in head and neck squamous cell carcinoma (HNSCC) Morgan, Ethan L. Toni, Tiffany Viswanathan, Ramya Robbins, Yvette Yang, Xinping Cheng, Hui Gunti, Sreenivasulu Huynh, Angel Sowers, Anastasia L. Mitchell, James B. Allen, Clint T. Chen, Zhong Van Waes, Carter Cell Death Differ Article TNFα is a key mediator of immune, chemotherapy and radiotherapy-induced cytotoxicity, but several cancers, including head and neck squamous cell carcinomas (HNSCC), display resistance to TNFα due to activation of the canonical NFκB pro-survival pathway. However, direct targeting of this pathway is associated with significant toxicity; thus, it is vital to identify novel mechanism(s) contributing to NFκB activation and TNFα resistance in cancer cells. Here, we demonstrate that the expression of proteasome-associated deubiquitinase USP14 is significantly increased in HNSCC and correlates with worse progression free survival in Human Papillomavirus (HPV)- HNSCC. Inhibition or depletion of USP14 inhibited the proliferation and survival of HNSCC cells. Further, USP14 inhibition reduced both basal and TNFα-inducible NFκB activity, NFκB-dependent gene expression and the nuclear translocation of the NFκB subunit RELA. Mechanistically, USP14 bound to both RELA and IκBα and reduced IκBα K48-ubiquitination leading to the degradation of IκBα, a critical inhibitor of the canonical NFκB pathway. Furthermore, we demonstrated that b-AP15, an inhibitor of USP14 and UCHL5, sensitized HNSCC cells to TNFα-mediated cell death, as well as radiation-induced cell death in vitro. Finally, b-AP15 delayed tumor growth and enhanced survival, both as a monotherapy and in combination with radiation, in HNSCC tumor xenograft models in vivo, which could be significantly attenuated by TNFα depletion. These data offer new insights into the activation of NFκB signaling in HNSCC and demonstrate that small molecule inhibitors targeting the ubiquitin pathway warrant further investigation as a novel therapeutic avenue to sensitize these cancers to TNFα- and radiation-induced cytotoxicity. Nature Publishing Group UK 2023-04-13 2023-05 /pmc/articles/PMC10154301/ /pubmed/37055579 http://dx.doi.org/10.1038/s41418-023-01144-x Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Morgan, Ethan L.
Toni, Tiffany
Viswanathan, Ramya
Robbins, Yvette
Yang, Xinping
Cheng, Hui
Gunti, Sreenivasulu
Huynh, Angel
Sowers, Anastasia L.
Mitchell, James B.
Allen, Clint T.
Chen, Zhong
Van Waes, Carter
Inhibition of USP14 promotes TNFα-induced cell death in head and neck squamous cell carcinoma (HNSCC)
title Inhibition of USP14 promotes TNFα-induced cell death in head and neck squamous cell carcinoma (HNSCC)
title_full Inhibition of USP14 promotes TNFα-induced cell death in head and neck squamous cell carcinoma (HNSCC)
title_fullStr Inhibition of USP14 promotes TNFα-induced cell death in head and neck squamous cell carcinoma (HNSCC)
title_full_unstemmed Inhibition of USP14 promotes TNFα-induced cell death in head and neck squamous cell carcinoma (HNSCC)
title_short Inhibition of USP14 promotes TNFα-induced cell death in head and neck squamous cell carcinoma (HNSCC)
title_sort inhibition of usp14 promotes tnfα-induced cell death in head and neck squamous cell carcinoma (hnscc)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154301/
https://www.ncbi.nlm.nih.gov/pubmed/37055579
http://dx.doi.org/10.1038/s41418-023-01144-x
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