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Automatic identification of small molecules that promote cell conversion and reprogramming
Controlling cell fate has great potential for regenerative medicine, drug discovery, and basic research. Although transcription factors are able to promote cell reprogramming and transdifferentiation, methods based on their upregulation often show low efficiency. Small molecules that can facilitate...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185468/ https://www.ncbi.nlm.nih.gov/pubmed/33891873 http://dx.doi.org/10.1016/j.stemcr.2021.03.028 |
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author | Napolitano, Francesco Rapakoulia, Trisevgeni Annunziata, Patrizia Hasegawa, Akira Cardon, Melissa Napolitano, Sara Vaccaro, Lorenzo Iuliano, Antonella Wanderlingh, Luca Giorgio Kasukawa, Takeya Medina, Diego L. Cacchiarelli, Davide Gao, Xin di Bernardo, Diego Arner, Erik |
author_facet | Napolitano, Francesco Rapakoulia, Trisevgeni Annunziata, Patrizia Hasegawa, Akira Cardon, Melissa Napolitano, Sara Vaccaro, Lorenzo Iuliano, Antonella Wanderlingh, Luca Giorgio Kasukawa, Takeya Medina, Diego L. Cacchiarelli, Davide Gao, Xin di Bernardo, Diego Arner, Erik |
author_sort | Napolitano, Francesco |
collection | PubMed |
description | Controlling cell fate has great potential for regenerative medicine, drug discovery, and basic research. Although transcription factors are able to promote cell reprogramming and transdifferentiation, methods based on their upregulation often show low efficiency. Small molecules that can facilitate conversion between cell types can ameliorate this problem working through safe, rapid, and reversible mechanisms. Here, we present DECCODE, an unbiased computational method for identification of such molecules based on transcriptional data. DECCODE matches a large collection of drug-induced profiles for drug treatments against a large dataset of primary cell transcriptional profiles to identify drugs that either alone or in combination enhance cell reprogramming and cell conversion. Extensive validation in the context of human induced pluripotent stem cells shows that DECCODE is able to prioritize drugs and drug combinations enhancing cell reprogramming. We also provide predictions for cell conversion with single drugs and drug combinations for 145 different cell types. |
format | Online Article Text |
id | pubmed-8185468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-81854682021-06-16 Automatic identification of small molecules that promote cell conversion and reprogramming Napolitano, Francesco Rapakoulia, Trisevgeni Annunziata, Patrizia Hasegawa, Akira Cardon, Melissa Napolitano, Sara Vaccaro, Lorenzo Iuliano, Antonella Wanderlingh, Luca Giorgio Kasukawa, Takeya Medina, Diego L. Cacchiarelli, Davide Gao, Xin di Bernardo, Diego Arner, Erik Stem Cell Reports Resource Controlling cell fate has great potential for regenerative medicine, drug discovery, and basic research. Although transcription factors are able to promote cell reprogramming and transdifferentiation, methods based on their upregulation often show low efficiency. Small molecules that can facilitate conversion between cell types can ameliorate this problem working through safe, rapid, and reversible mechanisms. Here, we present DECCODE, an unbiased computational method for identification of such molecules based on transcriptional data. DECCODE matches a large collection of drug-induced profiles for drug treatments against a large dataset of primary cell transcriptional profiles to identify drugs that either alone or in combination enhance cell reprogramming and cell conversion. Extensive validation in the context of human induced pluripotent stem cells shows that DECCODE is able to prioritize drugs and drug combinations enhancing cell reprogramming. We also provide predictions for cell conversion with single drugs and drug combinations for 145 different cell types. Elsevier 2021-04-22 /pmc/articles/PMC8185468/ /pubmed/33891873 http://dx.doi.org/10.1016/j.stemcr.2021.03.028 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Resource Napolitano, Francesco Rapakoulia, Trisevgeni Annunziata, Patrizia Hasegawa, Akira Cardon, Melissa Napolitano, Sara Vaccaro, Lorenzo Iuliano, Antonella Wanderlingh, Luca Giorgio Kasukawa, Takeya Medina, Diego L. Cacchiarelli, Davide Gao, Xin di Bernardo, Diego Arner, Erik Automatic identification of small molecules that promote cell conversion and reprogramming |
title | Automatic identification of small molecules that promote cell conversion and reprogramming |
title_full | Automatic identification of small molecules that promote cell conversion and reprogramming |
title_fullStr | Automatic identification of small molecules that promote cell conversion and reprogramming |
title_full_unstemmed | Automatic identification of small molecules that promote cell conversion and reprogramming |
title_short | Automatic identification of small molecules that promote cell conversion and reprogramming |
title_sort | automatic identification of small molecules that promote cell conversion and reprogramming |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185468/ https://www.ncbi.nlm.nih.gov/pubmed/33891873 http://dx.doi.org/10.1016/j.stemcr.2021.03.028 |
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