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Identification of a Novel Bcl-2 Inhibitor by Ligand-Based Screening and Investigation of Its Anti-cancer Effect on Human Breast Cancer Cells

Bcl-2 family protein is an important factor in regulating apoptosis and is associated with cancer. The anti-apoptotic proteins of Bcl-2 family, such as Bcl-2, are overexpression in numerous tumors, and contribute to cancer formation, development, and therapy resistance. Therefore, Bcl-2 is a promisi...

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Autores principales: Wen, Mei, Deng, Zhen-ke, Jiang, Shi-long, Guan, Yi-di, Wu, Hai-zhou, Wang, Xin-luan, Xiao, Song-shu, Zhang, Yi, Yang, Jin-ming, Cao, Dong-sheng, Cheng, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478794/
https://www.ncbi.nlm.nih.gov/pubmed/31057406
http://dx.doi.org/10.3389/fphar.2019.00391
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author Wen, Mei
Deng, Zhen-ke
Jiang, Shi-long
Guan, Yi-di
Wu, Hai-zhou
Wang, Xin-luan
Xiao, Song-shu
Zhang, Yi
Yang, Jin-ming
Cao, Dong-sheng
Cheng, Yan
author_facet Wen, Mei
Deng, Zhen-ke
Jiang, Shi-long
Guan, Yi-di
Wu, Hai-zhou
Wang, Xin-luan
Xiao, Song-shu
Zhang, Yi
Yang, Jin-ming
Cao, Dong-sheng
Cheng, Yan
author_sort Wen, Mei
collection PubMed
description Bcl-2 family protein is an important factor in regulating apoptosis and is associated with cancer. The anti-apoptotic proteins of Bcl-2 family, such as Bcl-2, are overexpression in numerous tumors, and contribute to cancer formation, development, and therapy resistance. Therefore, Bcl-2 is a promising target for drug development, and several Bcl-2 inhibitors are currently undergoing clinical trials. In this study, we carried out a QSAR-based virtual screening approach to develop potential Bcl-2 inhibitors from the SPECS database. Surface plasmon resonance (SPR) binding assay was performed to examine the interaction between Bcl-2 protein and the screened inhibitors. After that, we measured the anti-tumor activities of the 8 candidate compounds, and found that compound M1 has significant cytotoxic effect on breast cancer cells. We further proved that compound M1 downregulated Bcl-2 expression and activated apoptosis by inducing mitochondrial dysfunction. In conclusion, we identified a novel Bcl-2 inhibitor by QSAR screening, which exerted significant cytotoxic activity in breast cancer cells through inducing mitochondria-mediated apoptosis.
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spelling pubmed-64787942019-05-03 Identification of a Novel Bcl-2 Inhibitor by Ligand-Based Screening and Investigation of Its Anti-cancer Effect on Human Breast Cancer Cells Wen, Mei Deng, Zhen-ke Jiang, Shi-long Guan, Yi-di Wu, Hai-zhou Wang, Xin-luan Xiao, Song-shu Zhang, Yi Yang, Jin-ming Cao, Dong-sheng Cheng, Yan Front Pharmacol Pharmacology Bcl-2 family protein is an important factor in regulating apoptosis and is associated with cancer. The anti-apoptotic proteins of Bcl-2 family, such as Bcl-2, are overexpression in numerous tumors, and contribute to cancer formation, development, and therapy resistance. Therefore, Bcl-2 is a promising target for drug development, and several Bcl-2 inhibitors are currently undergoing clinical trials. In this study, we carried out a QSAR-based virtual screening approach to develop potential Bcl-2 inhibitors from the SPECS database. Surface plasmon resonance (SPR) binding assay was performed to examine the interaction between Bcl-2 protein and the screened inhibitors. After that, we measured the anti-tumor activities of the 8 candidate compounds, and found that compound M1 has significant cytotoxic effect on breast cancer cells. We further proved that compound M1 downregulated Bcl-2 expression and activated apoptosis by inducing mitochondrial dysfunction. In conclusion, we identified a novel Bcl-2 inhibitor by QSAR screening, which exerted significant cytotoxic activity in breast cancer cells through inducing mitochondria-mediated apoptosis. Frontiers Media S.A. 2019-04-17 /pmc/articles/PMC6478794/ /pubmed/31057406 http://dx.doi.org/10.3389/fphar.2019.00391 Text en Copyright © 2019 Wen, Deng, Jiang, Guan, Wu, Wang, Xiao, Zhang, Yang, Cao and Cheng. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Wen, Mei
Deng, Zhen-ke
Jiang, Shi-long
Guan, Yi-di
Wu, Hai-zhou
Wang, Xin-luan
Xiao, Song-shu
Zhang, Yi
Yang, Jin-ming
Cao, Dong-sheng
Cheng, Yan
Identification of a Novel Bcl-2 Inhibitor by Ligand-Based Screening and Investigation of Its Anti-cancer Effect on Human Breast Cancer Cells
title Identification of a Novel Bcl-2 Inhibitor by Ligand-Based Screening and Investigation of Its Anti-cancer Effect on Human Breast Cancer Cells
title_full Identification of a Novel Bcl-2 Inhibitor by Ligand-Based Screening and Investigation of Its Anti-cancer Effect on Human Breast Cancer Cells
title_fullStr Identification of a Novel Bcl-2 Inhibitor by Ligand-Based Screening and Investigation of Its Anti-cancer Effect on Human Breast Cancer Cells
title_full_unstemmed Identification of a Novel Bcl-2 Inhibitor by Ligand-Based Screening and Investigation of Its Anti-cancer Effect on Human Breast Cancer Cells
title_short Identification of a Novel Bcl-2 Inhibitor by Ligand-Based Screening and Investigation of Its Anti-cancer Effect on Human Breast Cancer Cells
title_sort identification of a novel bcl-2 inhibitor by ligand-based screening and investigation of its anti-cancer effect on human breast cancer cells
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478794/
https://www.ncbi.nlm.nih.gov/pubmed/31057406
http://dx.doi.org/10.3389/fphar.2019.00391
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