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The cornucopia of meaningful leads: Applying deep adversarial autoencoders for new molecule development in oncology
Recent advances in deep learning and specifically in generative adversarial networks have demonstrated surprising results in generating new images and videos upon request even using natural language as input. In this paper we present the first application of generative adversarial autoencoders (AAE)...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355231/ https://www.ncbi.nlm.nih.gov/pubmed/28029644 http://dx.doi.org/10.18632/oncotarget.14073 |
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author | Kadurin, Artur Aliper, Alexander Kazennov, Andrey Mamoshina, Polina Vanhaelen, Quentin Khrabrov, Kuzma Zhavoronkov, Alex |
author_facet | Kadurin, Artur Aliper, Alexander Kazennov, Andrey Mamoshina, Polina Vanhaelen, Quentin Khrabrov, Kuzma Zhavoronkov, Alex |
author_sort | Kadurin, Artur |
collection | PubMed |
description | Recent advances in deep learning and specifically in generative adversarial networks have demonstrated surprising results in generating new images and videos upon request even using natural language as input. In this paper we present the first application of generative adversarial autoencoders (AAE) for generating novel molecular fingerprints with a defined set of parameters. We developed a 7-layer AAE architecture with the latent middle layer serving as a discriminator. As an input and output the AAE uses a vector of binary fingerprints and concentration of the molecule. In the latent layer we also introduced a neuron responsible for growth inhibition percentage, which when negative indicates the reduction in the number of tumor cells after the treatment. To train the AAE we used the NCI-60 cell line assay data for 6252 compounds profiled on MCF-7 cell line. The output of the AAE was used to screen 72 million compounds in PubChem and select candidate molecules with potential anti-cancer properties. This approach is a proof of concept of an artificially-intelligent drug discovery engine, where AAEs are used to generate new molecular fingerprints with the desired molecular properties. |
format | Online Article Text |
id | pubmed-5355231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53552312017-04-26 The cornucopia of meaningful leads: Applying deep adversarial autoencoders for new molecule development in oncology Kadurin, Artur Aliper, Alexander Kazennov, Andrey Mamoshina, Polina Vanhaelen, Quentin Khrabrov, Kuzma Zhavoronkov, Alex Oncotarget Research Paper Recent advances in deep learning and specifically in generative adversarial networks have demonstrated surprising results in generating new images and videos upon request even using natural language as input. In this paper we present the first application of generative adversarial autoencoders (AAE) for generating novel molecular fingerprints with a defined set of parameters. We developed a 7-layer AAE architecture with the latent middle layer serving as a discriminator. As an input and output the AAE uses a vector of binary fingerprints and concentration of the molecule. In the latent layer we also introduced a neuron responsible for growth inhibition percentage, which when negative indicates the reduction in the number of tumor cells after the treatment. To train the AAE we used the NCI-60 cell line assay data for 6252 compounds profiled on MCF-7 cell line. The output of the AAE was used to screen 72 million compounds in PubChem and select candidate molecules with potential anti-cancer properties. This approach is a proof of concept of an artificially-intelligent drug discovery engine, where AAEs are used to generate new molecular fingerprints with the desired molecular properties. Impact Journals LLC 2016-12-22 /pmc/articles/PMC5355231/ /pubmed/28029644 http://dx.doi.org/10.18632/oncotarget.14073 Text en Copyright: © 2017 Kadurin et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Kadurin, Artur Aliper, Alexander Kazennov, Andrey Mamoshina, Polina Vanhaelen, Quentin Khrabrov, Kuzma Zhavoronkov, Alex The cornucopia of meaningful leads: Applying deep adversarial autoencoders for new molecule development in oncology |
title | The cornucopia of meaningful leads: Applying deep adversarial autoencoders for new molecule development in oncology |
title_full | The cornucopia of meaningful leads: Applying deep adversarial autoencoders for new molecule development in oncology |
title_fullStr | The cornucopia of meaningful leads: Applying deep adversarial autoencoders for new molecule development in oncology |
title_full_unstemmed | The cornucopia of meaningful leads: Applying deep adversarial autoencoders for new molecule development in oncology |
title_short | The cornucopia of meaningful leads: Applying deep adversarial autoencoders for new molecule development in oncology |
title_sort | cornucopia of meaningful leads: applying deep adversarial autoencoders for new molecule development in oncology |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355231/ https://www.ncbi.nlm.nih.gov/pubmed/28029644 http://dx.doi.org/10.18632/oncotarget.14073 |
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