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Architecture of The Human Ape1 Interactome Defines Novel Cancers Signatures
APE1 is essential in cancer cells due to its central role in the Base Excision Repair pathway of DNA lesions and in the transcriptional regulation of genes involved in tumor progression/chemoresistance. Indeed, APE1 overexpression correlates with chemoresistance in more aggressive cancers, and APE1...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949240/ https://www.ncbi.nlm.nih.gov/pubmed/31913336 http://dx.doi.org/10.1038/s41598-019-56981-z |
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author | Ayyildiz, Dilara Antoniali, Giulia D’Ambrosio, Chiara Mangiapane, Giovanna Dalla, Emiliano Scaloni, Andrea Tell, Gianluca Piazza, Silvano |
author_facet | Ayyildiz, Dilara Antoniali, Giulia D’Ambrosio, Chiara Mangiapane, Giovanna Dalla, Emiliano Scaloni, Andrea Tell, Gianluca Piazza, Silvano |
author_sort | Ayyildiz, Dilara |
collection | PubMed |
description | APE1 is essential in cancer cells due to its central role in the Base Excision Repair pathway of DNA lesions and in the transcriptional regulation of genes involved in tumor progression/chemoresistance. Indeed, APE1 overexpression correlates with chemoresistance in more aggressive cancers, and APE1 protein-protein interactions (PPIs) specifically modulate different protein functions in cancer cells. Although important, a detailed investigation on the nature and function of protein interactors regulating APE1 role in tumor progression and chemoresistance is still lacking. The present work was aimed at analyzing the APE1-PPI network with the goal of defining bad prognosis signatures through systematic bioinformatics analysis. By using a well-characterized HeLa cell model stably expressing a flagged APE1 form, which was subjected to extensive proteomics analyses for immunocaptured complexes from different subcellular compartments, we here demonstrate that APE1 is a central hub connecting different subnetworks largely composed of proteins belonging to cancer-associated communities and/or involved in RNA- and DNA-metabolism. When we performed survival analysis in real cancer datasets, we observed that more than 80% of these APE1-PPI network elements is associated with bad prognosis. Our findings, which are hypothesis generating, strongly support the possibility to infer APE1-interactomic signatures associated with bad prognosis of different cancers; they will be of general interest for the future definition of novel predictive disease biomarkers. Future studies will be needed to assess the function of APE1 in the protein complexes we discovered. Data are available via ProteomeXchange with identifier PXD013368. |
format | Online Article Text |
id | pubmed-6949240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69492402020-01-13 Architecture of The Human Ape1 Interactome Defines Novel Cancers Signatures Ayyildiz, Dilara Antoniali, Giulia D’Ambrosio, Chiara Mangiapane, Giovanna Dalla, Emiliano Scaloni, Andrea Tell, Gianluca Piazza, Silvano Sci Rep Article APE1 is essential in cancer cells due to its central role in the Base Excision Repair pathway of DNA lesions and in the transcriptional regulation of genes involved in tumor progression/chemoresistance. Indeed, APE1 overexpression correlates with chemoresistance in more aggressive cancers, and APE1 protein-protein interactions (PPIs) specifically modulate different protein functions in cancer cells. Although important, a detailed investigation on the nature and function of protein interactors regulating APE1 role in tumor progression and chemoresistance is still lacking. The present work was aimed at analyzing the APE1-PPI network with the goal of defining bad prognosis signatures through systematic bioinformatics analysis. By using a well-characterized HeLa cell model stably expressing a flagged APE1 form, which was subjected to extensive proteomics analyses for immunocaptured complexes from different subcellular compartments, we here demonstrate that APE1 is a central hub connecting different subnetworks largely composed of proteins belonging to cancer-associated communities and/or involved in RNA- and DNA-metabolism. When we performed survival analysis in real cancer datasets, we observed that more than 80% of these APE1-PPI network elements is associated with bad prognosis. Our findings, which are hypothesis generating, strongly support the possibility to infer APE1-interactomic signatures associated with bad prognosis of different cancers; they will be of general interest for the future definition of novel predictive disease biomarkers. Future studies will be needed to assess the function of APE1 in the protein complexes we discovered. Data are available via ProteomeXchange with identifier PXD013368. Nature Publishing Group UK 2020-01-08 /pmc/articles/PMC6949240/ /pubmed/31913336 http://dx.doi.org/10.1038/s41598-019-56981-z Text en © The Author(s) 2020 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 Ayyildiz, Dilara Antoniali, Giulia D’Ambrosio, Chiara Mangiapane, Giovanna Dalla, Emiliano Scaloni, Andrea Tell, Gianluca Piazza, Silvano Architecture of The Human Ape1 Interactome Defines Novel Cancers Signatures |
title | Architecture of The Human Ape1 Interactome Defines Novel Cancers Signatures |
title_full | Architecture of The Human Ape1 Interactome Defines Novel Cancers Signatures |
title_fullStr | Architecture of The Human Ape1 Interactome Defines Novel Cancers Signatures |
title_full_unstemmed | Architecture of The Human Ape1 Interactome Defines Novel Cancers Signatures |
title_short | Architecture of The Human Ape1 Interactome Defines Novel Cancers Signatures |
title_sort | architecture of the human ape1 interactome defines novel cancers signatures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949240/ https://www.ncbi.nlm.nih.gov/pubmed/31913336 http://dx.doi.org/10.1038/s41598-019-56981-z |
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