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2‐anilino‐4‐amino‐5‐aroylthiazole‐type compound AS7128 inhibits lung cancer growth through decreased iASPP and p53 interaction

Lung cancer is the leading cause of cancer‐related death worldwide. Thus, developing novel therapeutic agents has become critical for lung cancer treatment. In this study, compound AS7128 was selected from a 2‐million entry chemical library screening and identified as a candidate drug against non‐sm...

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Autores principales: Cheng, Hao‐Wei, Chein, Rong‐Jie, Cheng, Ting‐Jen, Wu, Pei‐Shan, Wu, Hsin‐Yi, Hung, Pei‐Fang, Wang, Chia‐Jen, Hsu, Yuan‐Ling, Wong, Jau‐Min, Yuan, Ang, Wong, Chi‐Huey, Yang, Pan‐Chyr, Pan, Szu‐Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834782/
https://www.ncbi.nlm.nih.gov/pubmed/29285847
http://dx.doi.org/10.1111/cas.13489
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author Cheng, Hao‐Wei
Chein, Rong‐Jie
Cheng, Ting‐Jen
Wu, Pei‐Shan
Wu, Hsin‐Yi
Hung, Pei‐Fang
Wang, Chia‐Jen
Hsu, Yuan‐Ling
Wong, Jau‐Min
Yuan, Ang
Wong, Chi‐Huey
Yang, Pan‐Chyr
Pan, Szu‐Hua
author_facet Cheng, Hao‐Wei
Chein, Rong‐Jie
Cheng, Ting‐Jen
Wu, Pei‐Shan
Wu, Hsin‐Yi
Hung, Pei‐Fang
Wang, Chia‐Jen
Hsu, Yuan‐Ling
Wong, Jau‐Min
Yuan, Ang
Wong, Chi‐Huey
Yang, Pan‐Chyr
Pan, Szu‐Hua
author_sort Cheng, Hao‐Wei
collection PubMed
description Lung cancer is the leading cause of cancer‐related death worldwide. Thus, developing novel therapeutic agents has become critical for lung cancer treatment. In this study, compound AS7128 was selected from a 2‐million entry chemical library screening and identified as a candidate drug against non‐small cell lung cancer in vitro and in vivo. Further investigation indicated that AS7128 could induce cell apoptosis and cell cycle arrest, especially in the mitosis stage. In addition, we also found that iASPP, an oncogenic protein that functionally inhibits p53, might be associated with AS7128 through mass identification. Further exploration indicated that AS7128 treatment could restore the transactivation ability of p53 and, thus, increase the expressions of its downstream target genes, which are related to cell cycle arrest and apoptosis. This occurs through disruption of the interactions between p53 and iASPP in cells. Taken together, AS7128 could bind to iASPP, disrupt the interaction between iASPP and p53, and result in cell cycle arrest and apoptosis. These findings may provide new insight for using iASPP as a therapeutic target for non‐small cell lung cancer treatment.
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spelling pubmed-58347822018-03-06 2‐anilino‐4‐amino‐5‐aroylthiazole‐type compound AS7128 inhibits lung cancer growth through decreased iASPP and p53 interaction Cheng, Hao‐Wei Chein, Rong‐Jie Cheng, Ting‐Jen Wu, Pei‐Shan Wu, Hsin‐Yi Hung, Pei‐Fang Wang, Chia‐Jen Hsu, Yuan‐Ling Wong, Jau‐Min Yuan, Ang Wong, Chi‐Huey Yang, Pan‐Chyr Pan, Szu‐Hua Cancer Sci Original Articles Lung cancer is the leading cause of cancer‐related death worldwide. Thus, developing novel therapeutic agents has become critical for lung cancer treatment. In this study, compound AS7128 was selected from a 2‐million entry chemical library screening and identified as a candidate drug against non‐small cell lung cancer in vitro and in vivo. Further investigation indicated that AS7128 could induce cell apoptosis and cell cycle arrest, especially in the mitosis stage. In addition, we also found that iASPP, an oncogenic protein that functionally inhibits p53, might be associated with AS7128 through mass identification. Further exploration indicated that AS7128 treatment could restore the transactivation ability of p53 and, thus, increase the expressions of its downstream target genes, which are related to cell cycle arrest and apoptosis. This occurs through disruption of the interactions between p53 and iASPP in cells. Taken together, AS7128 could bind to iASPP, disrupt the interaction between iASPP and p53, and result in cell cycle arrest and apoptosis. These findings may provide new insight for using iASPP as a therapeutic target for non‐small cell lung cancer treatment. John Wiley and Sons Inc. 2018-02-06 2018-03 /pmc/articles/PMC5834782/ /pubmed/29285847 http://dx.doi.org/10.1111/cas.13489 Text en © 2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Cheng, Hao‐Wei
Chein, Rong‐Jie
Cheng, Ting‐Jen
Wu, Pei‐Shan
Wu, Hsin‐Yi
Hung, Pei‐Fang
Wang, Chia‐Jen
Hsu, Yuan‐Ling
Wong, Jau‐Min
Yuan, Ang
Wong, Chi‐Huey
Yang, Pan‐Chyr
Pan, Szu‐Hua
2‐anilino‐4‐amino‐5‐aroylthiazole‐type compound AS7128 inhibits lung cancer growth through decreased iASPP and p53 interaction
title 2‐anilino‐4‐amino‐5‐aroylthiazole‐type compound AS7128 inhibits lung cancer growth through decreased iASPP and p53 interaction
title_full 2‐anilino‐4‐amino‐5‐aroylthiazole‐type compound AS7128 inhibits lung cancer growth through decreased iASPP and p53 interaction
title_fullStr 2‐anilino‐4‐amino‐5‐aroylthiazole‐type compound AS7128 inhibits lung cancer growth through decreased iASPP and p53 interaction
title_full_unstemmed 2‐anilino‐4‐amino‐5‐aroylthiazole‐type compound AS7128 inhibits lung cancer growth through decreased iASPP and p53 interaction
title_short 2‐anilino‐4‐amino‐5‐aroylthiazole‐type compound AS7128 inhibits lung cancer growth through decreased iASPP and p53 interaction
title_sort 2‐anilino‐4‐amino‐5‐aroylthiazole‐type compound as7128 inhibits lung cancer growth through decreased iaspp and p53 interaction
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834782/
https://www.ncbi.nlm.nih.gov/pubmed/29285847
http://dx.doi.org/10.1111/cas.13489
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