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Bortezomib Congeners Induce Apoptosis of Hepatocellular Carcinoma via CIP2A Inhibition

CIP2A is an oncoprotein that upregulates p-Akt and promotes cancer cell proliferation and survival. The proteasome inhibitor bortezomib has been shown to reduce CIP2A and lead to cell apoptosis. Here; we modified the functional group of bortezomib to generate a series of novel compounds and conducte...

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Autores principales: Hou, Duen-Ren, Huang, Ann-Chi, Shiau, Chung-Wai, Wang, Chun-Yi, Yu, Hui-Chuan, Chen, Kuen-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269665/
https://www.ncbi.nlm.nih.gov/pubmed/24335617
http://dx.doi.org/10.3390/molecules181215398
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author Hou, Duen-Ren
Huang, Ann-Chi
Shiau, Chung-Wai
Wang, Chun-Yi
Yu, Hui-Chuan
Chen, Kuen-Feng
author_facet Hou, Duen-Ren
Huang, Ann-Chi
Shiau, Chung-Wai
Wang, Chun-Yi
Yu, Hui-Chuan
Chen, Kuen-Feng
author_sort Hou, Duen-Ren
collection PubMed
description CIP2A is an oncoprotein that upregulates p-Akt and promotes cancer cell proliferation and survival. The proteasome inhibitor bortezomib has been shown to reduce CIP2A and lead to cell apoptosis. Here; we modified the functional group of bortezomib to generate a series of novel compounds and conducted a structure–activity relationship (SAR) study. The results showed that compound 1 was able to repress CIP2A expression and cell apoptosis in the same manner as bortezomib, but with less potency in inhibition of proteasome activity. This finding provides a new direction for the design of CIP2A inhibitors.
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spelling pubmed-62696652018-12-20 Bortezomib Congeners Induce Apoptosis of Hepatocellular Carcinoma via CIP2A Inhibition Hou, Duen-Ren Huang, Ann-Chi Shiau, Chung-Wai Wang, Chun-Yi Yu, Hui-Chuan Chen, Kuen-Feng Molecules Article CIP2A is an oncoprotein that upregulates p-Akt and promotes cancer cell proliferation and survival. The proteasome inhibitor bortezomib has been shown to reduce CIP2A and lead to cell apoptosis. Here; we modified the functional group of bortezomib to generate a series of novel compounds and conducted a structure–activity relationship (SAR) study. The results showed that compound 1 was able to repress CIP2A expression and cell apoptosis in the same manner as bortezomib, but with less potency in inhibition of proteasome activity. This finding provides a new direction for the design of CIP2A inhibitors. MDPI 2013-12-11 /pmc/articles/PMC6269665/ /pubmed/24335617 http://dx.doi.org/10.3390/molecules181215398 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Hou, Duen-Ren
Huang, Ann-Chi
Shiau, Chung-Wai
Wang, Chun-Yi
Yu, Hui-Chuan
Chen, Kuen-Feng
Bortezomib Congeners Induce Apoptosis of Hepatocellular Carcinoma via CIP2A Inhibition
title Bortezomib Congeners Induce Apoptosis of Hepatocellular Carcinoma via CIP2A Inhibition
title_full Bortezomib Congeners Induce Apoptosis of Hepatocellular Carcinoma via CIP2A Inhibition
title_fullStr Bortezomib Congeners Induce Apoptosis of Hepatocellular Carcinoma via CIP2A Inhibition
title_full_unstemmed Bortezomib Congeners Induce Apoptosis of Hepatocellular Carcinoma via CIP2A Inhibition
title_short Bortezomib Congeners Induce Apoptosis of Hepatocellular Carcinoma via CIP2A Inhibition
title_sort bortezomib congeners induce apoptosis of hepatocellular carcinoma via cip2a inhibition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269665/
https://www.ncbi.nlm.nih.gov/pubmed/24335617
http://dx.doi.org/10.3390/molecules181215398
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