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Facilitating Anti-Cancer Combinatorial Drug Discovery by Targeting Epistatic Disease Genes
Due to synergistic effects, combinatorial drugs are widely used for treating complex diseases. However, combining drugs and making them synergetic remains a challenge. Genetic disease genes are considered a promising source of drug targets with important implications for navigating the drug space. M...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017788/ https://www.ncbi.nlm.nih.gov/pubmed/29570606 http://dx.doi.org/10.3390/molecules23040736 |
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author | Quan, Yuan Liu, Meng-Yuan Liu, Ye-Mao Zhu, Li-Da Wu, Yu-Shan Luo, Zhi-Hui Zhang, Xiu-Zhen Xu, Shi-Zhong Yang, Qing-Yong Zhang, Hong-Yu |
author_facet | Quan, Yuan Liu, Meng-Yuan Liu, Ye-Mao Zhu, Li-Da Wu, Yu-Shan Luo, Zhi-Hui Zhang, Xiu-Zhen Xu, Shi-Zhong Yang, Qing-Yong Zhang, Hong-Yu |
author_sort | Quan, Yuan |
collection | PubMed |
description | Due to synergistic effects, combinatorial drugs are widely used for treating complex diseases. However, combining drugs and making them synergetic remains a challenge. Genetic disease genes are considered a promising source of drug targets with important implications for navigating the drug space. Most diseases are not caused by a single pathogenic factor, but by multiple disease genes, in particular, interacting disease genes. Thus, it is reasonable to consider that targeting epistatic disease genes may enhance the therapeutic effects of combinatorial drugs. In this study, synthetic lethality gene pairs of tumors, similar to epistatic disease genes, were first targeted by combinatorial drugs, resulting in the enrichment of the combinatorial drugs with cancer treatment, which verified our hypothesis. Then, conventional epistasis detection software was used to identify epistatic disease genes from the genome wide association studies (GWAS) dataset. Furthermore, combinatorial drugs were predicted by targeting these epistatic disease genes, and five combinations were proven to have synergistic anti-cancer effects on MCF-7 cells through cell cytotoxicity assay. Combined with the three-dimensional (3D) genome-based method, the epistatic disease genes were filtered and were more closely related to disease. By targeting the filtered gene pairs, the efficiency of combinatorial drug discovery has been further improved. |
format | Online Article Text |
id | pubmed-6017788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60177882018-11-13 Facilitating Anti-Cancer Combinatorial Drug Discovery by Targeting Epistatic Disease Genes Quan, Yuan Liu, Meng-Yuan Liu, Ye-Mao Zhu, Li-Da Wu, Yu-Shan Luo, Zhi-Hui Zhang, Xiu-Zhen Xu, Shi-Zhong Yang, Qing-Yong Zhang, Hong-Yu Molecules Article Due to synergistic effects, combinatorial drugs are widely used for treating complex diseases. However, combining drugs and making them synergetic remains a challenge. Genetic disease genes are considered a promising source of drug targets with important implications for navigating the drug space. Most diseases are not caused by a single pathogenic factor, but by multiple disease genes, in particular, interacting disease genes. Thus, it is reasonable to consider that targeting epistatic disease genes may enhance the therapeutic effects of combinatorial drugs. In this study, synthetic lethality gene pairs of tumors, similar to epistatic disease genes, were first targeted by combinatorial drugs, resulting in the enrichment of the combinatorial drugs with cancer treatment, which verified our hypothesis. Then, conventional epistasis detection software was used to identify epistatic disease genes from the genome wide association studies (GWAS) dataset. Furthermore, combinatorial drugs were predicted by targeting these epistatic disease genes, and five combinations were proven to have synergistic anti-cancer effects on MCF-7 cells through cell cytotoxicity assay. Combined with the three-dimensional (3D) genome-based method, the epistatic disease genes were filtered and were more closely related to disease. By targeting the filtered gene pairs, the efficiency of combinatorial drug discovery has been further improved. MDPI 2018-03-23 /pmc/articles/PMC6017788/ /pubmed/29570606 http://dx.doi.org/10.3390/molecules23040736 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Quan, Yuan Liu, Meng-Yuan Liu, Ye-Mao Zhu, Li-Da Wu, Yu-Shan Luo, Zhi-Hui Zhang, Xiu-Zhen Xu, Shi-Zhong Yang, Qing-Yong Zhang, Hong-Yu Facilitating Anti-Cancer Combinatorial Drug Discovery by Targeting Epistatic Disease Genes |
title | Facilitating Anti-Cancer Combinatorial Drug Discovery by Targeting Epistatic Disease Genes |
title_full | Facilitating Anti-Cancer Combinatorial Drug Discovery by Targeting Epistatic Disease Genes |
title_fullStr | Facilitating Anti-Cancer Combinatorial Drug Discovery by Targeting Epistatic Disease Genes |
title_full_unstemmed | Facilitating Anti-Cancer Combinatorial Drug Discovery by Targeting Epistatic Disease Genes |
title_short | Facilitating Anti-Cancer Combinatorial Drug Discovery by Targeting Epistatic Disease Genes |
title_sort | facilitating anti-cancer combinatorial drug discovery by targeting epistatic disease genes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017788/ https://www.ncbi.nlm.nih.gov/pubmed/29570606 http://dx.doi.org/10.3390/molecules23040736 |
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