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PC3T: a signature-driven predictor of chemical compounds for cellular transition
Cellular transitions hold great promise in translational medicine research. However, therapeutic applications are limited by the low efficiency and safety concerns of using transcription factors. Small molecules provide a temporal and highly tunable approach to overcome these issues. Here, we presen...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533498/ https://www.ncbi.nlm.nih.gov/pubmed/37758874 http://dx.doi.org/10.1038/s42003-023-05225-y |
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author | Han, Lu Song, Bin Zhang, Peilin Zhong, Zhi Zhang, Yongxiang Bo, Xiaochen Wang, Hongyang Zhang, Yong Cui, Xiuliang Zhou, Wenxia |
author_facet | Han, Lu Song, Bin Zhang, Peilin Zhong, Zhi Zhang, Yongxiang Bo, Xiaochen Wang, Hongyang Zhang, Yong Cui, Xiuliang Zhou, Wenxia |
author_sort | Han, Lu |
collection | PubMed |
description | Cellular transitions hold great promise in translational medicine research. However, therapeutic applications are limited by the low efficiency and safety concerns of using transcription factors. Small molecules provide a temporal and highly tunable approach to overcome these issues. Here, we present PC3T, a computational framework to enrich molecules that induce desired cellular transitions, and PC3T was able to consistently enrich small molecules that had been experimentally validated in both bulk and single-cell datasets. We then predicted small molecule reprogramming of fibroblasts into hepatic progenitor-like cells (HPLCs). The converted cells exhibited epithelial cell-like morphology and HPLC-like gene expression pattern. Hepatic functions were also observed, such as glycogen storage and lipid accumulation. Finally, we collected and manually curated a cell state transition resource containing 224 time-course gene expression datasets and 153 cell types. Our framework, together with the data resource, is freely available at http://pc3t.idrug.net.cn/. We believe that PC3T is a powerful tool to promote chemical-induced cell state transitions. |
format | Online Article Text |
id | pubmed-10533498 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105334982023-09-29 PC3T: a signature-driven predictor of chemical compounds for cellular transition Han, Lu Song, Bin Zhang, Peilin Zhong, Zhi Zhang, Yongxiang Bo, Xiaochen Wang, Hongyang Zhang, Yong Cui, Xiuliang Zhou, Wenxia Commun Biol Article Cellular transitions hold great promise in translational medicine research. However, therapeutic applications are limited by the low efficiency and safety concerns of using transcription factors. Small molecules provide a temporal and highly tunable approach to overcome these issues. Here, we present PC3T, a computational framework to enrich molecules that induce desired cellular transitions, and PC3T was able to consistently enrich small molecules that had been experimentally validated in both bulk and single-cell datasets. We then predicted small molecule reprogramming of fibroblasts into hepatic progenitor-like cells (HPLCs). The converted cells exhibited epithelial cell-like morphology and HPLC-like gene expression pattern. Hepatic functions were also observed, such as glycogen storage and lipid accumulation. Finally, we collected and manually curated a cell state transition resource containing 224 time-course gene expression datasets and 153 cell types. Our framework, together with the data resource, is freely available at http://pc3t.idrug.net.cn/. We believe that PC3T is a powerful tool to promote chemical-induced cell state transitions. Nature Publishing Group UK 2023-09-27 /pmc/articles/PMC10533498/ /pubmed/37758874 http://dx.doi.org/10.1038/s42003-023-05225-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Han, Lu Song, Bin Zhang, Peilin Zhong, Zhi Zhang, Yongxiang Bo, Xiaochen Wang, Hongyang Zhang, Yong Cui, Xiuliang Zhou, Wenxia PC3T: a signature-driven predictor of chemical compounds for cellular transition |
title | PC3T: a signature-driven predictor of chemical compounds for cellular transition |
title_full | PC3T: a signature-driven predictor of chemical compounds for cellular transition |
title_fullStr | PC3T: a signature-driven predictor of chemical compounds for cellular transition |
title_full_unstemmed | PC3T: a signature-driven predictor of chemical compounds for cellular transition |
title_short | PC3T: a signature-driven predictor of chemical compounds for cellular transition |
title_sort | pc3t: a signature-driven predictor of chemical compounds for cellular transition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533498/ https://www.ncbi.nlm.nih.gov/pubmed/37758874 http://dx.doi.org/10.1038/s42003-023-05225-y |
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