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Epigenetic targeting drugs potentiate chemotherapeutic effects in solid tumor therapy
Epigenetic therapy is a novel tumor therapeutic method and refers to the targeting of the aberrant epigenetic modifications presumably at cancer-related genes by chemicals which are epigenetic targeting drugs (ETDs). Not like in treating hematopoietic cancer, the clinical trials investigating the po...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481380/ https://www.ncbi.nlm.nih.gov/pubmed/28642588 http://dx.doi.org/10.1038/s41598-017-04406-0 |
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author | Li, Jingjing Hao, Dapeng Wang, Li Wang, Haitao Wang, Yuan Zhao, Zhiqiang Li, Peipei Deng, Chuxia Di, Li-jun |
author_facet | Li, Jingjing Hao, Dapeng Wang, Li Wang, Haitao Wang, Yuan Zhao, Zhiqiang Li, Peipei Deng, Chuxia Di, Li-jun |
author_sort | Li, Jingjing |
collection | PubMed |
description | Epigenetic therapy is a novel tumor therapeutic method and refers to the targeting of the aberrant epigenetic modifications presumably at cancer-related genes by chemicals which are epigenetic targeting drugs (ETDs). Not like in treating hematopoietic cancer, the clinical trials investigating the potential use of ETDs in the solid tumor is not encouraging. Instead, the curative effects of ETD delivered together with DNA targeting chemo drugs (DTDs) are quite promising according to our meta-analysis. To investigate the synergistic mechanism of ETD and DTD drug combination, the therapeutic effect was studied using both cell lines and mouse engrafted tumors. Mechanically we show that HDAC inhibitors and DNMT inhibitors are capable of increasing the chromatin accessibility to cisplatin (CP) and doxorubicin (Dox) through chromatin decompaction globally. Consequently, the combination of ETD and DTD enhances the DTD induced DNA damage and cell death. Engrafted tumors in SCID mice also show increased sensitivity to irradiation (IR) or CP when the tumors were pretreated by ETDs. Given the limited therapeutic effect of ETD alone, these results strongly suggest that the combination of DTD, including irradiation, and ETD treatment is a very promising choice in clinical solid tumor therapy. |
format | Online Article Text |
id | pubmed-5481380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54813802017-06-26 Epigenetic targeting drugs potentiate chemotherapeutic effects in solid tumor therapy Li, Jingjing Hao, Dapeng Wang, Li Wang, Haitao Wang, Yuan Zhao, Zhiqiang Li, Peipei Deng, Chuxia Di, Li-jun Sci Rep Article Epigenetic therapy is a novel tumor therapeutic method and refers to the targeting of the aberrant epigenetic modifications presumably at cancer-related genes by chemicals which are epigenetic targeting drugs (ETDs). Not like in treating hematopoietic cancer, the clinical trials investigating the potential use of ETDs in the solid tumor is not encouraging. Instead, the curative effects of ETD delivered together with DNA targeting chemo drugs (DTDs) are quite promising according to our meta-analysis. To investigate the synergistic mechanism of ETD and DTD drug combination, the therapeutic effect was studied using both cell lines and mouse engrafted tumors. Mechanically we show that HDAC inhibitors and DNMT inhibitors are capable of increasing the chromatin accessibility to cisplatin (CP) and doxorubicin (Dox) through chromatin decompaction globally. Consequently, the combination of ETD and DTD enhances the DTD induced DNA damage and cell death. Engrafted tumors in SCID mice also show increased sensitivity to irradiation (IR) or CP when the tumors were pretreated by ETDs. Given the limited therapeutic effect of ETD alone, these results strongly suggest that the combination of DTD, including irradiation, and ETD treatment is a very promising choice in clinical solid tumor therapy. Nature Publishing Group UK 2017-06-22 /pmc/articles/PMC5481380/ /pubmed/28642588 http://dx.doi.org/10.1038/s41598-017-04406-0 Text en © The Author(s) 2017 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 Li, Jingjing Hao, Dapeng Wang, Li Wang, Haitao Wang, Yuan Zhao, Zhiqiang Li, Peipei Deng, Chuxia Di, Li-jun Epigenetic targeting drugs potentiate chemotherapeutic effects in solid tumor therapy |
title | Epigenetic targeting drugs potentiate chemotherapeutic effects in solid tumor therapy |
title_full | Epigenetic targeting drugs potentiate chemotherapeutic effects in solid tumor therapy |
title_fullStr | Epigenetic targeting drugs potentiate chemotherapeutic effects in solid tumor therapy |
title_full_unstemmed | Epigenetic targeting drugs potentiate chemotherapeutic effects in solid tumor therapy |
title_short | Epigenetic targeting drugs potentiate chemotherapeutic effects in solid tumor therapy |
title_sort | epigenetic targeting drugs potentiate chemotherapeutic effects in solid tumor therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481380/ https://www.ncbi.nlm.nih.gov/pubmed/28642588 http://dx.doi.org/10.1038/s41598-017-04406-0 |
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