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Vorinostat enhances the cisplatin-mediated anticancer effects in small cell lung cancer cells

BACKGROUND: Vorinostat, a histone deacetylase (HDAC) inhibitor, is a promising agent for cancer therapy. Combining vorinostat with cisplatin may relax the chromatin structure and facilitate the accessibility of cisplatin, thus enhancing its cytotoxicity. Studies have not yet investigated the effects...

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Autores principales: Pan, Chun-Hao, Chang, Ying-Fang, Lee, Ming-Shuo, Wen, B-Chen, Ko, Jen-Chung, Liang, Sheng-Kai, Liang, Mei-Chih
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100277/
https://www.ncbi.nlm.nih.gov/pubmed/27821078
http://dx.doi.org/10.1186/s12885-016-2888-7
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author Pan, Chun-Hao
Chang, Ying-Fang
Lee, Ming-Shuo
Wen, B-Chen
Ko, Jen-Chung
Liang, Sheng-Kai
Liang, Mei-Chih
author_facet Pan, Chun-Hao
Chang, Ying-Fang
Lee, Ming-Shuo
Wen, B-Chen
Ko, Jen-Chung
Liang, Sheng-Kai
Liang, Mei-Chih
author_sort Pan, Chun-Hao
collection PubMed
description BACKGROUND: Vorinostat, a histone deacetylase (HDAC) inhibitor, is a promising agent for cancer therapy. Combining vorinostat with cisplatin may relax the chromatin structure and facilitate the accessibility of cisplatin, thus enhancing its cytotoxicity. Studies have not yet investigated the effects of the combination of vorinostat and cisplatin on small cell lung cancer (SCLC). METHODS: We first assessed the efficacy of vorinostat with etoposide/cisplatin (EP; triple combination) and then investigated the effects of cotreatment with vorinostat and cisplatin on H209 and H146 SCLC cell lines. The anticancer effects of various combinations were determined in terms of cell viability, apoptosis, cell cycle distribution, and vorinostat-regulated proteins. We also evaluated the efficacy of vorinostat/cisplatin combination in H209 xenograft nude mice. RESULTS: Our data revealed that the triple combination engendered a significant reduction of cell viability and high apoptotic cell death. In addition, vorinostat combined with cisplatin enhanced cell growth inhibition, induced apoptosis, and promoted cell cycle arrest. We observed that the acetylation levels of histone H3 and α-tubulin were higher in combination treatments than in vorinostat treatment alone. Moreover, vorinostat reduced the expression of thymidylate synthase (TS), and TS remained inhibited after cotreament with cisplatin. Furthermore, an in vivo study revealed that the combination of vorinostat and cisplatin significantly inhibited tumor growth in xenograft nude mice (tumor growth inhibition T/C% = 20.5 %). CONCLUSIONS: Combined treatments with vorinostat promote the cytotoxicity of cisplatin and induce the expression of vorinostat-regulated acetyl proteins, eventually enhancing antitumor effects in SCLC cell lines. Triple combinations with a low dosage of cisplatin demonstrate similar therapeutic effects. Such triple combinations, if applied clinically, may reduce the undesired adverse effects of cisplatin. The effects of the combination of vorinostat and cisplatin should be evaluated further before conducting clinical trials for SCLC treatment.
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spelling pubmed-51002772016-11-08 Vorinostat enhances the cisplatin-mediated anticancer effects in small cell lung cancer cells Pan, Chun-Hao Chang, Ying-Fang Lee, Ming-Shuo Wen, B-Chen Ko, Jen-Chung Liang, Sheng-Kai Liang, Mei-Chih BMC Cancer Research Article BACKGROUND: Vorinostat, a histone deacetylase (HDAC) inhibitor, is a promising agent for cancer therapy. Combining vorinostat with cisplatin may relax the chromatin structure and facilitate the accessibility of cisplatin, thus enhancing its cytotoxicity. Studies have not yet investigated the effects of the combination of vorinostat and cisplatin on small cell lung cancer (SCLC). METHODS: We first assessed the efficacy of vorinostat with etoposide/cisplatin (EP; triple combination) and then investigated the effects of cotreatment with vorinostat and cisplatin on H209 and H146 SCLC cell lines. The anticancer effects of various combinations were determined in terms of cell viability, apoptosis, cell cycle distribution, and vorinostat-regulated proteins. We also evaluated the efficacy of vorinostat/cisplatin combination in H209 xenograft nude mice. RESULTS: Our data revealed that the triple combination engendered a significant reduction of cell viability and high apoptotic cell death. In addition, vorinostat combined with cisplatin enhanced cell growth inhibition, induced apoptosis, and promoted cell cycle arrest. We observed that the acetylation levels of histone H3 and α-tubulin were higher in combination treatments than in vorinostat treatment alone. Moreover, vorinostat reduced the expression of thymidylate synthase (TS), and TS remained inhibited after cotreament with cisplatin. Furthermore, an in vivo study revealed that the combination of vorinostat and cisplatin significantly inhibited tumor growth in xenograft nude mice (tumor growth inhibition T/C% = 20.5 %). CONCLUSIONS: Combined treatments with vorinostat promote the cytotoxicity of cisplatin and induce the expression of vorinostat-regulated acetyl proteins, eventually enhancing antitumor effects in SCLC cell lines. Triple combinations with a low dosage of cisplatin demonstrate similar therapeutic effects. Such triple combinations, if applied clinically, may reduce the undesired adverse effects of cisplatin. The effects of the combination of vorinostat and cisplatin should be evaluated further before conducting clinical trials for SCLC treatment. BioMed Central 2016-11-07 /pmc/articles/PMC5100277/ /pubmed/27821078 http://dx.doi.org/10.1186/s12885-016-2888-7 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Pan, Chun-Hao
Chang, Ying-Fang
Lee, Ming-Shuo
Wen, B-Chen
Ko, Jen-Chung
Liang, Sheng-Kai
Liang, Mei-Chih
Vorinostat enhances the cisplatin-mediated anticancer effects in small cell lung cancer cells
title Vorinostat enhances the cisplatin-mediated anticancer effects in small cell lung cancer cells
title_full Vorinostat enhances the cisplatin-mediated anticancer effects in small cell lung cancer cells
title_fullStr Vorinostat enhances the cisplatin-mediated anticancer effects in small cell lung cancer cells
title_full_unstemmed Vorinostat enhances the cisplatin-mediated anticancer effects in small cell lung cancer cells
title_short Vorinostat enhances the cisplatin-mediated anticancer effects in small cell lung cancer cells
title_sort vorinostat enhances the cisplatin-mediated anticancer effects in small cell lung cancer cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100277/
https://www.ncbi.nlm.nih.gov/pubmed/27821078
http://dx.doi.org/10.1186/s12885-016-2888-7
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