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High mobility group box 1 promotes radioresistance in esophageal squamous cell carcinoma cell lines by modulating autophagy
Resistance to radiotherapy results in relapse and treatment failure in locally advanced esophageal squamous cell carcinoma (ESCC). High mobility group box 1 (HMGB1) is reported to be associated with the radioresistance in bladder and breast cancer. However, the role of HMGB1 in the radiotherapy resp...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372718/ https://www.ncbi.nlm.nih.gov/pubmed/30755598 http://dx.doi.org/10.1038/s41419-019-1355-1 |
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author | Ma, Hongbing Zheng, Shuyu Zhang, Xiaozhi Gong, Tuotuo Lv, Xin Fu, Shenbo Zhang, Shuqun Yin, Xiaoran Hao, Jingcan Shan, Changyou Huang, Shan |
author_facet | Ma, Hongbing Zheng, Shuyu Zhang, Xiaozhi Gong, Tuotuo Lv, Xin Fu, Shenbo Zhang, Shuqun Yin, Xiaoran Hao, Jingcan Shan, Changyou Huang, Shan |
author_sort | Ma, Hongbing |
collection | PubMed |
description | Resistance to radiotherapy results in relapse and treatment failure in locally advanced esophageal squamous cell carcinoma (ESCC). High mobility group box 1 (HMGB1) is reported to be associated with the radioresistance in bladder and breast cancer. However, the role of HMGB1 in the radiotherapy response in ESCC has not been fully elucidated. Here, we investigated the role of HMGB1 to radioresistance in ESCC clinical samples and cell lines. We found that HMGB1 expression was associated with tumor recurrence after postoperative radiotherapy in locally advanced ESCC patients. HMGB1 knockdown in ESCC cells resulted in increased radiosensitivity both in vitro and in vivo. Autophagy level was found depressed in HMGB1 inhibition cells and activation of autophagy brought back cell’s radioresistance. Our results demonstrate that HMGB1 activate autophagy and consequently promote radioresistance. HMGB1 may be used as a predictor of poor response to radiotherapy in ESCC patients. Our finding also highlights the importance of the utility of HMGB1 in ESCC radiosensitization. |
format | Online Article Text |
id | pubmed-6372718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63727182019-02-13 High mobility group box 1 promotes radioresistance in esophageal squamous cell carcinoma cell lines by modulating autophagy Ma, Hongbing Zheng, Shuyu Zhang, Xiaozhi Gong, Tuotuo Lv, Xin Fu, Shenbo Zhang, Shuqun Yin, Xiaoran Hao, Jingcan Shan, Changyou Huang, Shan Cell Death Dis Article Resistance to radiotherapy results in relapse and treatment failure in locally advanced esophageal squamous cell carcinoma (ESCC). High mobility group box 1 (HMGB1) is reported to be associated with the radioresistance in bladder and breast cancer. However, the role of HMGB1 in the radiotherapy response in ESCC has not been fully elucidated. Here, we investigated the role of HMGB1 to radioresistance in ESCC clinical samples and cell lines. We found that HMGB1 expression was associated with tumor recurrence after postoperative radiotherapy in locally advanced ESCC patients. HMGB1 knockdown in ESCC cells resulted in increased radiosensitivity both in vitro and in vivo. Autophagy level was found depressed in HMGB1 inhibition cells and activation of autophagy brought back cell’s radioresistance. Our results demonstrate that HMGB1 activate autophagy and consequently promote radioresistance. HMGB1 may be used as a predictor of poor response to radiotherapy in ESCC patients. Our finding also highlights the importance of the utility of HMGB1 in ESCC radiosensitization. Nature Publishing Group UK 2019-02-12 /pmc/articles/PMC6372718/ /pubmed/30755598 http://dx.doi.org/10.1038/s41419-019-1355-1 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 Ma, Hongbing Zheng, Shuyu Zhang, Xiaozhi Gong, Tuotuo Lv, Xin Fu, Shenbo Zhang, Shuqun Yin, Xiaoran Hao, Jingcan Shan, Changyou Huang, Shan High mobility group box 1 promotes radioresistance in esophageal squamous cell carcinoma cell lines by modulating autophagy |
title | High mobility group box 1 promotes radioresistance in esophageal squamous cell carcinoma cell lines by modulating autophagy |
title_full | High mobility group box 1 promotes radioresistance in esophageal squamous cell carcinoma cell lines by modulating autophagy |
title_fullStr | High mobility group box 1 promotes radioresistance in esophageal squamous cell carcinoma cell lines by modulating autophagy |
title_full_unstemmed | High mobility group box 1 promotes radioresistance in esophageal squamous cell carcinoma cell lines by modulating autophagy |
title_short | High mobility group box 1 promotes radioresistance in esophageal squamous cell carcinoma cell lines by modulating autophagy |
title_sort | high mobility group box 1 promotes radioresistance in esophageal squamous cell carcinoma cell lines by modulating autophagy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372718/ https://www.ncbi.nlm.nih.gov/pubmed/30755598 http://dx.doi.org/10.1038/s41419-019-1355-1 |
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