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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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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. |
format | Online Article Text |
id | pubmed-5834782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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