Cargando…
ProTargetMiner as a proteome signature library of anticancer molecules for functional discovery
Deconvolution of targets and action mechanisms of anticancer compounds is fundamental in drug development. Here, we report on ProTargetMiner as a publicly available expandable proteome signature library of anticancer molecules in cancer cell lines. Based on 287 A549 adenocarcinoma proteomes affected...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915695/ https://www.ncbi.nlm.nih.gov/pubmed/31844049 http://dx.doi.org/10.1038/s41467-019-13582-8 |
_version_ | 1783480076222857216 |
---|---|
author | Saei, Amir Ata Beusch, Christian Michel Chernobrovkin, Alexey Sabatier, Pierre Zhang, Bo Tokat, Ülkü Güler Stergiou, Eleni Gaetani, Massimiliano Végvári, Ákos Zubarev, Roman A. |
author_facet | Saei, Amir Ata Beusch, Christian Michel Chernobrovkin, Alexey Sabatier, Pierre Zhang, Bo Tokat, Ülkü Güler Stergiou, Eleni Gaetani, Massimiliano Végvári, Ákos Zubarev, Roman A. |
author_sort | Saei, Amir Ata |
collection | PubMed |
description | Deconvolution of targets and action mechanisms of anticancer compounds is fundamental in drug development. Here, we report on ProTargetMiner as a publicly available expandable proteome signature library of anticancer molecules in cancer cell lines. Based on 287 A549 adenocarcinoma proteomes affected by 56 compounds, the main dataset contains 7,328 proteins and 1,307,859 refined protein-drug pairs. These proteomic signatures cluster by compound targets and action mechanisms. The targets and mechanistic proteins are deconvoluted by partial least square modeling, provided through the website http://protargetminer.genexplain.com. For 9 molecules representing the most diverse mechanisms and the common cancer cell lines MCF-7, RKO and A549, deep proteome datasets are obtained. Combining data from the three cell lines highlights common drug targets and cell-specific differences. The database can be easily extended and merged with new compound signatures. ProTargetMiner serves as a chemical proteomics resource for the cancer research community, and can become a valuable tool in drug discovery. |
format | Online Article Text |
id | pubmed-6915695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69156952019-12-18 ProTargetMiner as a proteome signature library of anticancer molecules for functional discovery Saei, Amir Ata Beusch, Christian Michel Chernobrovkin, Alexey Sabatier, Pierre Zhang, Bo Tokat, Ülkü Güler Stergiou, Eleni Gaetani, Massimiliano Végvári, Ákos Zubarev, Roman A. Nat Commun Article Deconvolution of targets and action mechanisms of anticancer compounds is fundamental in drug development. Here, we report on ProTargetMiner as a publicly available expandable proteome signature library of anticancer molecules in cancer cell lines. Based on 287 A549 adenocarcinoma proteomes affected by 56 compounds, the main dataset contains 7,328 proteins and 1,307,859 refined protein-drug pairs. These proteomic signatures cluster by compound targets and action mechanisms. The targets and mechanistic proteins are deconvoluted by partial least square modeling, provided through the website http://protargetminer.genexplain.com. For 9 molecules representing the most diverse mechanisms and the common cancer cell lines MCF-7, RKO and A549, deep proteome datasets are obtained. Combining data from the three cell lines highlights common drug targets and cell-specific differences. The database can be easily extended and merged with new compound signatures. ProTargetMiner serves as a chemical proteomics resource for the cancer research community, and can become a valuable tool in drug discovery. Nature Publishing Group UK 2019-12-16 /pmc/articles/PMC6915695/ /pubmed/31844049 http://dx.doi.org/10.1038/s41467-019-13582-8 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Saei, Amir Ata Beusch, Christian Michel Chernobrovkin, Alexey Sabatier, Pierre Zhang, Bo Tokat, Ülkü Güler Stergiou, Eleni Gaetani, Massimiliano Végvári, Ákos Zubarev, Roman A. ProTargetMiner as a proteome signature library of anticancer molecules for functional discovery |
title | ProTargetMiner as a proteome signature library of anticancer molecules for functional discovery |
title_full | ProTargetMiner as a proteome signature library of anticancer molecules for functional discovery |
title_fullStr | ProTargetMiner as a proteome signature library of anticancer molecules for functional discovery |
title_full_unstemmed | ProTargetMiner as a proteome signature library of anticancer molecules for functional discovery |
title_short | ProTargetMiner as a proteome signature library of anticancer molecules for functional discovery |
title_sort | protargetminer as a proteome signature library of anticancer molecules for functional discovery |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915695/ https://www.ncbi.nlm.nih.gov/pubmed/31844049 http://dx.doi.org/10.1038/s41467-019-13582-8 |
work_keys_str_mv | AT saeiamirata protargetminerasaproteomesignaturelibraryofanticancermoleculesforfunctionaldiscovery AT beuschchristianmichel protargetminerasaproteomesignaturelibraryofanticancermoleculesforfunctionaldiscovery AT chernobrovkinalexey protargetminerasaproteomesignaturelibraryofanticancermoleculesforfunctionaldiscovery AT sabatierpierre protargetminerasaproteomesignaturelibraryofanticancermoleculesforfunctionaldiscovery AT zhangbo protargetminerasaproteomesignaturelibraryofanticancermoleculesforfunctionaldiscovery AT tokatulkuguler protargetminerasaproteomesignaturelibraryofanticancermoleculesforfunctionaldiscovery AT stergioueleni protargetminerasaproteomesignaturelibraryofanticancermoleculesforfunctionaldiscovery AT gaetanimassimiliano protargetminerasaproteomesignaturelibraryofanticancermoleculesforfunctionaldiscovery AT vegvariakos protargetminerasaproteomesignaturelibraryofanticancermoleculesforfunctionaldiscovery AT zubarevromana protargetminerasaproteomesignaturelibraryofanticancermoleculesforfunctionaldiscovery |