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TNFα promotes oral cancer growth, pain, and Schwann cell activation
Oral cancer is very painful and impairs a patient’s ability to eat, talk, and drink. Mediators secreted from oral cancer can excite and sensitize sensory neurons inducing pain. Cancer mediators can also activate Schwann cells, the peripheral glia that regulates neuronal function and repair. The cont...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815837/ https://www.ncbi.nlm.nih.gov/pubmed/33469141 http://dx.doi.org/10.1038/s41598-021-81500-4 |
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author | Salvo, Elizabeth Tu, Nguyen H. Scheff, Nicole N. Dubeykovskaya, Zinaida A. Chavan, Shruti A. Aouizerat, Bradley E. Ye, Yi |
author_facet | Salvo, Elizabeth Tu, Nguyen H. Scheff, Nicole N. Dubeykovskaya, Zinaida A. Chavan, Shruti A. Aouizerat, Bradley E. Ye, Yi |
author_sort | Salvo, Elizabeth |
collection | PubMed |
description | Oral cancer is very painful and impairs a patient’s ability to eat, talk, and drink. Mediators secreted from oral cancer can excite and sensitize sensory neurons inducing pain. Cancer mediators can also activate Schwann cells, the peripheral glia that regulates neuronal function and repair. The contribution of Schwann cells to oral cancer pain is unclear. We hypothesize that the oral cancer mediator TNFα activates Schwann cells, which further promotes cancer progression and pain. We demonstrate that TNFα is overexpressed in human oral cancer tissues and correlates with increased self-reported pain in patients. Antagonizing TNFα reduces oral cancer proliferation, cytokine production, and nociception in mice with oral cancer. Oral cancer or TNFα alone increases Schwann cell activation (measured by Schwann cell proliferation, migration, and activation markers), which can be inhibited by neutralizing TNFα. Cancer- or TNFα-activated Schwann cells release pro-nociceptive mediators such as TNFα and nerve growth factor (NGF). Activated Schwann cells induce nociceptive behaviors in mice, which is alleviated by blocking TNFα. Our study suggests that TNFα promotes cancer proliferation, progression, and nociception at least partially by activating Schwann cells. Inhibiting TNFα or Schwann cell activation might serve as therapeutic approaches for the treatment of oral cancer and associated pain. |
format | Online Article Text |
id | pubmed-7815837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78158372021-01-21 TNFα promotes oral cancer growth, pain, and Schwann cell activation Salvo, Elizabeth Tu, Nguyen H. Scheff, Nicole N. Dubeykovskaya, Zinaida A. Chavan, Shruti A. Aouizerat, Bradley E. Ye, Yi Sci Rep Article Oral cancer is very painful and impairs a patient’s ability to eat, talk, and drink. Mediators secreted from oral cancer can excite and sensitize sensory neurons inducing pain. Cancer mediators can also activate Schwann cells, the peripheral glia that regulates neuronal function and repair. The contribution of Schwann cells to oral cancer pain is unclear. We hypothesize that the oral cancer mediator TNFα activates Schwann cells, which further promotes cancer progression and pain. We demonstrate that TNFα is overexpressed in human oral cancer tissues and correlates with increased self-reported pain in patients. Antagonizing TNFα reduces oral cancer proliferation, cytokine production, and nociception in mice with oral cancer. Oral cancer or TNFα alone increases Schwann cell activation (measured by Schwann cell proliferation, migration, and activation markers), which can be inhibited by neutralizing TNFα. Cancer- or TNFα-activated Schwann cells release pro-nociceptive mediators such as TNFα and nerve growth factor (NGF). Activated Schwann cells induce nociceptive behaviors in mice, which is alleviated by blocking TNFα. Our study suggests that TNFα promotes cancer proliferation, progression, and nociception at least partially by activating Schwann cells. Inhibiting TNFα or Schwann cell activation might serve as therapeutic approaches for the treatment of oral cancer and associated pain. Nature Publishing Group UK 2021-01-19 /pmc/articles/PMC7815837/ /pubmed/33469141 http://dx.doi.org/10.1038/s41598-021-81500-4 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Salvo, Elizabeth Tu, Nguyen H. Scheff, Nicole N. Dubeykovskaya, Zinaida A. Chavan, Shruti A. Aouizerat, Bradley E. Ye, Yi TNFα promotes oral cancer growth, pain, and Schwann cell activation |
title | TNFα promotes oral cancer growth, pain, and Schwann cell activation |
title_full | TNFα promotes oral cancer growth, pain, and Schwann cell activation |
title_fullStr | TNFα promotes oral cancer growth, pain, and Schwann cell activation |
title_full_unstemmed | TNFα promotes oral cancer growth, pain, and Schwann cell activation |
title_short | TNFα promotes oral cancer growth, pain, and Schwann cell activation |
title_sort | tnfα promotes oral cancer growth, pain, and schwann cell activation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815837/ https://www.ncbi.nlm.nih.gov/pubmed/33469141 http://dx.doi.org/10.1038/s41598-021-81500-4 |
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