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Tanshinone sensitized the antitumor effects of irradiation on laryngeal cancer via JNK pathway
Laryngeal cancer is a common cancer occurred in the head and neck. Irradiation sensitivity is a problem affecting the treatment of laryngeal cancer. Tanshinone IIA has been reported to play an important role in treating multiple diseases; yet, whether Tanshinone IIA can be an irradiation sensitizer...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198231/ https://www.ncbi.nlm.nih.gov/pubmed/30239172 http://dx.doi.org/10.1002/cam4.1781 |
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author | Xu, Hui Hao, Yu‐li Xu, Li‐na Chen, Liang Xu, Feng‐wei |
author_facet | Xu, Hui Hao, Yu‐li Xu, Li‐na Chen, Liang Xu, Feng‐wei |
author_sort | Xu, Hui |
collection | PubMed |
description | Laryngeal cancer is a common cancer occurred in the head and neck. Irradiation sensitivity is a problem affecting the treatment of laryngeal cancer. Tanshinone IIA has been reported to play an important role in treating multiple diseases; yet, whether Tanshinone IIA can be an irradiation sensitizer has not been reported. Clonogenic assay, annexin‐V/propidium iodide double‐staining assay, and Cell Counting Kit‐8 assay were performed to detect cell survival, proliferation, apoptosis, and viability. Mouse laryngeal cancer xenograft model was established and subjected to tumor size analysis. Tanshinone IIA treatment increased the irradiation sensitivity of laryngeal cancer cells by reducing cell survival, viability and proliferation, and increasing cell apoptosis. Tanshinone IIA treatment increased the survival period of mice in the in vivo laryngeal cancer model, evidenced by decreased growth and weight of tumors, which was possibly mediated through the JNK pathway. Tanshinone IIA increases the sensitivity to irradiation in laryngeal cancer cells and in vivo laryngeal cancer model, suggesting that Tanshinone IIA can be a therapeutic antitumor agent for treating laryngeal cancer. |
format | Online Article Text |
id | pubmed-6198231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61982312018-10-31 Tanshinone sensitized the antitumor effects of irradiation on laryngeal cancer via JNK pathway Xu, Hui Hao, Yu‐li Xu, Li‐na Chen, Liang Xu, Feng‐wei Cancer Med Cancer Biology Laryngeal cancer is a common cancer occurred in the head and neck. Irradiation sensitivity is a problem affecting the treatment of laryngeal cancer. Tanshinone IIA has been reported to play an important role in treating multiple diseases; yet, whether Tanshinone IIA can be an irradiation sensitizer has not been reported. Clonogenic assay, annexin‐V/propidium iodide double‐staining assay, and Cell Counting Kit‐8 assay were performed to detect cell survival, proliferation, apoptosis, and viability. Mouse laryngeal cancer xenograft model was established and subjected to tumor size analysis. Tanshinone IIA treatment increased the irradiation sensitivity of laryngeal cancer cells by reducing cell survival, viability and proliferation, and increasing cell apoptosis. Tanshinone IIA treatment increased the survival period of mice in the in vivo laryngeal cancer model, evidenced by decreased growth and weight of tumors, which was possibly mediated through the JNK pathway. Tanshinone IIA increases the sensitivity to irradiation in laryngeal cancer cells and in vivo laryngeal cancer model, suggesting that Tanshinone IIA can be a therapeutic antitumor agent for treating laryngeal cancer. John Wiley and Sons Inc. 2018-09-21 /pmc/articles/PMC6198231/ /pubmed/30239172 http://dx.doi.org/10.1002/cam4.1781 Text en © 2018 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Cancer Biology Xu, Hui Hao, Yu‐li Xu, Li‐na Chen, Liang Xu, Feng‐wei Tanshinone sensitized the antitumor effects of irradiation on laryngeal cancer via JNK pathway |
title | Tanshinone sensitized the antitumor effects of irradiation on laryngeal cancer via JNK pathway |
title_full | Tanshinone sensitized the antitumor effects of irradiation on laryngeal cancer via JNK pathway |
title_fullStr | Tanshinone sensitized the antitumor effects of irradiation on laryngeal cancer via JNK pathway |
title_full_unstemmed | Tanshinone sensitized the antitumor effects of irradiation on laryngeal cancer via JNK pathway |
title_short | Tanshinone sensitized the antitumor effects of irradiation on laryngeal cancer via JNK pathway |
title_sort | tanshinone sensitized the antitumor effects of irradiation on laryngeal cancer via jnk pathway |
topic | Cancer Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198231/ https://www.ncbi.nlm.nih.gov/pubmed/30239172 http://dx.doi.org/10.1002/cam4.1781 |
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