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Repositioning antipsychotic chlorpromazine for treating colorectal cancer by inhibiting sirtuin 1
Investigating existing drugs for repositioning can enable overcoming bottlenecks in the drug development process. Here, we investigated the effect and molecular mechanism of the antipsychotic drug chlorpromazine (CPZ) and identified its potential for treating colorectal cancer (CRC). Human CRC cell...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4695010/ https://www.ncbi.nlm.nih.gov/pubmed/26363315 |
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author | Lee, Wen-Ying Lee, Wai-Theng Cheng, Chia-Hsiung Chen, Ku-Chung Chou, Chih-Ming Chung, Chu-Hung Sun, Min-Siou Cheng, Hung-Wei Ho, Meng-Ni Lin, Cheng-Wei |
author_facet | Lee, Wen-Ying Lee, Wai-Theng Cheng, Chia-Hsiung Chen, Ku-Chung Chou, Chih-Ming Chung, Chu-Hung Sun, Min-Siou Cheng, Hung-Wei Ho, Meng-Ni Lin, Cheng-Wei |
author_sort | Lee, Wen-Ying |
collection | PubMed |
description | Investigating existing drugs for repositioning can enable overcoming bottlenecks in the drug development process. Here, we investigated the effect and molecular mechanism of the antipsychotic drug chlorpromazine (CPZ) and identified its potential for treating colorectal cancer (CRC). Human CRC cell lines harboring different p53 statuses were used to investigate the inhibitory mechanism of CPZ. CPZ effectively inhibited tumor growth and induced apoptosis in CRC cells in a p53-dependent manner. Activation of c-jun N-terminal kinase (JNK) was crucial for CPZ-induced p53 expression and the subsequent induction of tumor apoptosis. Induction of p53 acetylation at lysine382 was involved in CPZ-mediated tumor apoptosis, and this induction was attenuated by sirtuin 1 (SIRT1), a class III histone deacetylase. By contrast, knocking down SIRT1 sensitized tumor cells to CPZ treatment. Moreover, CPZ induced the degradation of SIRT1 protein participating downstream of JNK, and JNK suppression abrogated CPZ-mediated SIRT1 downregulation. Clinical analysis revealed a significant association between high SIRT1 expression and poor outcome in CRC patients. These data suggest that SIRT1 is an attractive therapeutic target for CRC and that CPZ is a potential repositioned drug for treating CRC. |
format | Online Article Text |
id | pubmed-4695010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-46950102016-01-20 Repositioning antipsychotic chlorpromazine for treating colorectal cancer by inhibiting sirtuin 1 Lee, Wen-Ying Lee, Wai-Theng Cheng, Chia-Hsiung Chen, Ku-Chung Chou, Chih-Ming Chung, Chu-Hung Sun, Min-Siou Cheng, Hung-Wei Ho, Meng-Ni Lin, Cheng-Wei Oncotarget Research Paper Investigating existing drugs for repositioning can enable overcoming bottlenecks in the drug development process. Here, we investigated the effect and molecular mechanism of the antipsychotic drug chlorpromazine (CPZ) and identified its potential for treating colorectal cancer (CRC). Human CRC cell lines harboring different p53 statuses were used to investigate the inhibitory mechanism of CPZ. CPZ effectively inhibited tumor growth and induced apoptosis in CRC cells in a p53-dependent manner. Activation of c-jun N-terminal kinase (JNK) was crucial for CPZ-induced p53 expression and the subsequent induction of tumor apoptosis. Induction of p53 acetylation at lysine382 was involved in CPZ-mediated tumor apoptosis, and this induction was attenuated by sirtuin 1 (SIRT1), a class III histone deacetylase. By contrast, knocking down SIRT1 sensitized tumor cells to CPZ treatment. Moreover, CPZ induced the degradation of SIRT1 protein participating downstream of JNK, and JNK suppression abrogated CPZ-mediated SIRT1 downregulation. Clinical analysis revealed a significant association between high SIRT1 expression and poor outcome in CRC patients. These data suggest that SIRT1 is an attractive therapeutic target for CRC and that CPZ is a potential repositioned drug for treating CRC. Impact Journals LLC 2015-09-05 /pmc/articles/PMC4695010/ /pubmed/26363315 Text en Copyright: © 2015 Lee et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Lee, Wen-Ying Lee, Wai-Theng Cheng, Chia-Hsiung Chen, Ku-Chung Chou, Chih-Ming Chung, Chu-Hung Sun, Min-Siou Cheng, Hung-Wei Ho, Meng-Ni Lin, Cheng-Wei Repositioning antipsychotic chlorpromazine for treating colorectal cancer by inhibiting sirtuin 1 |
title | Repositioning antipsychotic chlorpromazine for treating colorectal cancer by inhibiting sirtuin 1 |
title_full | Repositioning antipsychotic chlorpromazine for treating colorectal cancer by inhibiting sirtuin 1 |
title_fullStr | Repositioning antipsychotic chlorpromazine for treating colorectal cancer by inhibiting sirtuin 1 |
title_full_unstemmed | Repositioning antipsychotic chlorpromazine for treating colorectal cancer by inhibiting sirtuin 1 |
title_short | Repositioning antipsychotic chlorpromazine for treating colorectal cancer by inhibiting sirtuin 1 |
title_sort | repositioning antipsychotic chlorpromazine for treating colorectal cancer by inhibiting sirtuin 1 |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4695010/ https://www.ncbi.nlm.nih.gov/pubmed/26363315 |
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