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An integrated multi-omics analysis of topoisomerase family in pan-cancer: Friend or foe?
BACKGROUND: Topoisomerases are nuclear enzymes that get to the bottom of topological troubles related with DNA all through a range of genetic procedures. More and more studies have shown that topoisomerase-mediated DNA cleavage plays crucial roles in tumor cell death and carcinogenesis. There is how...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604985/ https://www.ncbi.nlm.nih.gov/pubmed/36288358 http://dx.doi.org/10.1371/journal.pone.0274546 |
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author | Zhou, Xin Yao, Guixiang Zhang, Jin Bian, Jiasheng Li, Guanghao Xu, Jianfeng |
author_facet | Zhou, Xin Yao, Guixiang Zhang, Jin Bian, Jiasheng Li, Guanghao Xu, Jianfeng |
author_sort | Zhou, Xin |
collection | PubMed |
description | BACKGROUND: Topoisomerases are nuclear enzymes that get to the bottom of topological troubles related with DNA all through a range of genetic procedures. More and more studies have shown that topoisomerase-mediated DNA cleavage plays crucial roles in tumor cell death and carcinogenesis. There is however still a lack of comprehensive multi-omics studies related to topoisomerase family genes from a pan-cancer perspective. METHODS: In this study, a multiomics pan-cancer analysis of topoisomerase family genes was conducted by integrating over 10,000 multi-dimensional cancer genomic data across 33 cancer types from The Cancer Genome Atlas (TCGA), 481 small molecule drug response data from cancer therapeutics response portal (CTRP) as well as normal tissue data from Genotype-Tissue Expression (GTEx). Finally, overall activity-level analyses of topoisomerase in pan-cancers were performed by gene set variation analysis (GSVA), together with differential expression, clinical relevancy, immune cell infiltration and regulation of cancer-related pathways. RESULTS: Dysregulated gene expression of topoisomerase family were related to genomic changes and abnormal epigenetic modifications. The expression levels of topoisomerase family genes could significantly impact cancer progression, intratumoral heterogeneity, alterations in the immunological condition and regulation of the cancer marker-related pathways, which in turn caused the differences in potential drugs sensitivity and the distinct prognosis of patients. CONCLUSION: It was anticipated that topoisomerase family genes would become novel prognostic biomarkers for cancer patients and provide new insights for the diagnosis and treatment of tumors. |
format | Online Article Text |
id | pubmed-9604985 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-96049852022-10-27 An integrated multi-omics analysis of topoisomerase family in pan-cancer: Friend or foe? Zhou, Xin Yao, Guixiang Zhang, Jin Bian, Jiasheng Li, Guanghao Xu, Jianfeng PLoS One Research Article BACKGROUND: Topoisomerases are nuclear enzymes that get to the bottom of topological troubles related with DNA all through a range of genetic procedures. More and more studies have shown that topoisomerase-mediated DNA cleavage plays crucial roles in tumor cell death and carcinogenesis. There is however still a lack of comprehensive multi-omics studies related to topoisomerase family genes from a pan-cancer perspective. METHODS: In this study, a multiomics pan-cancer analysis of topoisomerase family genes was conducted by integrating over 10,000 multi-dimensional cancer genomic data across 33 cancer types from The Cancer Genome Atlas (TCGA), 481 small molecule drug response data from cancer therapeutics response portal (CTRP) as well as normal tissue data from Genotype-Tissue Expression (GTEx). Finally, overall activity-level analyses of topoisomerase in pan-cancers were performed by gene set variation analysis (GSVA), together with differential expression, clinical relevancy, immune cell infiltration and regulation of cancer-related pathways. RESULTS: Dysregulated gene expression of topoisomerase family were related to genomic changes and abnormal epigenetic modifications. The expression levels of topoisomerase family genes could significantly impact cancer progression, intratumoral heterogeneity, alterations in the immunological condition and regulation of the cancer marker-related pathways, which in turn caused the differences in potential drugs sensitivity and the distinct prognosis of patients. CONCLUSION: It was anticipated that topoisomerase family genes would become novel prognostic biomarkers for cancer patients and provide new insights for the diagnosis and treatment of tumors. Public Library of Science 2022-10-26 /pmc/articles/PMC9604985/ /pubmed/36288358 http://dx.doi.org/10.1371/journal.pone.0274546 Text en © 2022 Zhou et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Zhou, Xin Yao, Guixiang Zhang, Jin Bian, Jiasheng Li, Guanghao Xu, Jianfeng An integrated multi-omics analysis of topoisomerase family in pan-cancer: Friend or foe? |
title | An integrated multi-omics analysis of topoisomerase family in pan-cancer: Friend or foe? |
title_full | An integrated multi-omics analysis of topoisomerase family in pan-cancer: Friend or foe? |
title_fullStr | An integrated multi-omics analysis of topoisomerase family in pan-cancer: Friend or foe? |
title_full_unstemmed | An integrated multi-omics analysis of topoisomerase family in pan-cancer: Friend or foe? |
title_short | An integrated multi-omics analysis of topoisomerase family in pan-cancer: Friend or foe? |
title_sort | integrated multi-omics analysis of topoisomerase family in pan-cancer: friend or foe? |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604985/ https://www.ncbi.nlm.nih.gov/pubmed/36288358 http://dx.doi.org/10.1371/journal.pone.0274546 |
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