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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
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.
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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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