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The synergistic effects of oxaliplatin and piperlongumine on colorectal cancer are mediated by oxidative stress
Oxaliplatin-based chemotherapy is recommended as the first-line therapeutic regimen for metastatic colorectal cancer. However, long-term and repeated oxaliplatin therapy leads to drug resistance and severe adverse events, which hamper its clinical application. Thus, chemosensitizers are urgently req...
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/PMC6687721/ https://www.ncbi.nlm.nih.gov/pubmed/31395855 http://dx.doi.org/10.1038/s41419-019-1824-6 |
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author | Chen, WeiQian Lian, WeiShuai Yuan, YiFeng Li, MaoQuan |
author_facet | Chen, WeiQian Lian, WeiShuai Yuan, YiFeng Li, MaoQuan |
author_sort | Chen, WeiQian |
collection | PubMed |
description | Oxaliplatin-based chemotherapy is recommended as the first-line therapeutic regimen for metastatic colorectal cancer. However, long-term and repeated oxaliplatin therapy leads to drug resistance and severe adverse events, which hamper its clinical application. Thus, chemosensitizers are urgently required for overcoming oxaliplatin resistance and toxicity. Here, the anticancer effects of oxaliplatin combined with piperlongumine (PL), a molecule promoting reactive oxygen species (ROS) generation, in colorectal cancer, were assessed. We demonstrated that oxaliplatin elevated cellular ROS amounts and showed synergistic anticancer effects with PL in colorectal cancer cells. These anticancer effects were mediated by mitochondrial dysfunction and endoplasmic reticulum (ER) stress apoptotic-associated networks. Meanwhile, blockage of ROS production prevented apoptosis and fully reversed mitochondrial dysfunction and ER stress associated with the oxaliplatin/PL combination. Moreover, xenograft assays in mouse models highly corroborated in vitro data. In conclusion, this study provides a novel combination therapy for colorectal cancer, and reveals that manipulating ROS production might constitute an effective tool for developing novel treatments in colorectal cancer. |
format | Online Article Text |
id | pubmed-6687721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66877212019-08-09 The synergistic effects of oxaliplatin and piperlongumine on colorectal cancer are mediated by oxidative stress Chen, WeiQian Lian, WeiShuai Yuan, YiFeng Li, MaoQuan Cell Death Dis Article Oxaliplatin-based chemotherapy is recommended as the first-line therapeutic regimen for metastatic colorectal cancer. However, long-term and repeated oxaliplatin therapy leads to drug resistance and severe adverse events, which hamper its clinical application. Thus, chemosensitizers are urgently required for overcoming oxaliplatin resistance and toxicity. Here, the anticancer effects of oxaliplatin combined with piperlongumine (PL), a molecule promoting reactive oxygen species (ROS) generation, in colorectal cancer, were assessed. We demonstrated that oxaliplatin elevated cellular ROS amounts and showed synergistic anticancer effects with PL in colorectal cancer cells. These anticancer effects were mediated by mitochondrial dysfunction and endoplasmic reticulum (ER) stress apoptotic-associated networks. Meanwhile, blockage of ROS production prevented apoptosis and fully reversed mitochondrial dysfunction and ER stress associated with the oxaliplatin/PL combination. Moreover, xenograft assays in mouse models highly corroborated in vitro data. In conclusion, this study provides a novel combination therapy for colorectal cancer, and reveals that manipulating ROS production might constitute an effective tool for developing novel treatments in colorectal cancer. Nature Publishing Group UK 2019-08-08 /pmc/articles/PMC6687721/ /pubmed/31395855 http://dx.doi.org/10.1038/s41419-019-1824-6 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 Chen, WeiQian Lian, WeiShuai Yuan, YiFeng Li, MaoQuan The synergistic effects of oxaliplatin and piperlongumine on colorectal cancer are mediated by oxidative stress |
title | The synergistic effects of oxaliplatin and piperlongumine on colorectal cancer are mediated by oxidative stress |
title_full | The synergistic effects of oxaliplatin and piperlongumine on colorectal cancer are mediated by oxidative stress |
title_fullStr | The synergistic effects of oxaliplatin and piperlongumine on colorectal cancer are mediated by oxidative stress |
title_full_unstemmed | The synergistic effects of oxaliplatin and piperlongumine on colorectal cancer are mediated by oxidative stress |
title_short | The synergistic effects of oxaliplatin and piperlongumine on colorectal cancer are mediated by oxidative stress |
title_sort | synergistic effects of oxaliplatin and piperlongumine on colorectal cancer are mediated by oxidative stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687721/ https://www.ncbi.nlm.nih.gov/pubmed/31395855 http://dx.doi.org/10.1038/s41419-019-1824-6 |
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