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Network-based identification of biomarkers for colon adenocarcinoma
BACKGROUND: As one of the most common cancers with high mortality in the world, we are still facing a huge challenge in the prevention and treatment of colon cancer. With the rapid development of high throughput technologies, new biomarkers identification for colon cancer has been confronted with th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367377/ https://www.ncbi.nlm.nih.gov/pubmed/32680494 http://dx.doi.org/10.1186/s12885-020-07157-w |
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author | Hu, Fuyan Wang, Qing Yang, Zhiyuan Zhang, Zeng Liu, Xiaoping |
author_facet | Hu, Fuyan Wang, Qing Yang, Zhiyuan Zhang, Zeng Liu, Xiaoping |
author_sort | Hu, Fuyan |
collection | PubMed |
description | BACKGROUND: As one of the most common cancers with high mortality in the world, we are still facing a huge challenge in the prevention and treatment of colon cancer. With the rapid development of high throughput technologies, new biomarkers identification for colon cancer has been confronted with the new opportunities and challenges. METHODS: We firstly constructed functional networks for each sample of colon adenocarcinoma (COAD) by using a sample-specific network (SSN) method which can construct individual-specific networks based on gene expression profiles of a single sample. The functional genes and interactions were identified from the functional networks, respectively. RESULTS: Classification and subtyping were used to test the function of the functional genes and interactions. The results of classification showed that the functional genes could be used as diagnostic biomarkers. The subtypes displayed different mechanisms, which were shown by the functional and pathway enrichment analysis for the representative genes of each subtype. Besides, subtype-specific molecular patterns were also detected, such as subtype-specific clinical and mutation features. Finally, 12 functional genes and 13 functional edges could serve as prognosis biomarkers since they were associated with the survival rate of COAD. CONCLUSIONS: In conclusion, the functional genes and interactions in the constructed functional network could be used as new biomarkers for COAD. |
format | Online Article Text |
id | pubmed-7367377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73673772020-07-20 Network-based identification of biomarkers for colon adenocarcinoma Hu, Fuyan Wang, Qing Yang, Zhiyuan Zhang, Zeng Liu, Xiaoping BMC Cancer Research Article BACKGROUND: As one of the most common cancers with high mortality in the world, we are still facing a huge challenge in the prevention and treatment of colon cancer. With the rapid development of high throughput technologies, new biomarkers identification for colon cancer has been confronted with the new opportunities and challenges. METHODS: We firstly constructed functional networks for each sample of colon adenocarcinoma (COAD) by using a sample-specific network (SSN) method which can construct individual-specific networks based on gene expression profiles of a single sample. The functional genes and interactions were identified from the functional networks, respectively. RESULTS: Classification and subtyping were used to test the function of the functional genes and interactions. The results of classification showed that the functional genes could be used as diagnostic biomarkers. The subtypes displayed different mechanisms, which were shown by the functional and pathway enrichment analysis for the representative genes of each subtype. Besides, subtype-specific molecular patterns were also detected, such as subtype-specific clinical and mutation features. Finally, 12 functional genes and 13 functional edges could serve as prognosis biomarkers since they were associated with the survival rate of COAD. CONCLUSIONS: In conclusion, the functional genes and interactions in the constructed functional network could be used as new biomarkers for COAD. BioMed Central 2020-07-17 /pmc/articles/PMC7367377/ /pubmed/32680494 http://dx.doi.org/10.1186/s12885-020-07157-w Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Hu, Fuyan Wang, Qing Yang, Zhiyuan Zhang, Zeng Liu, Xiaoping Network-based identification of biomarkers for colon adenocarcinoma |
title | Network-based identification of biomarkers for colon adenocarcinoma |
title_full | Network-based identification of biomarkers for colon adenocarcinoma |
title_fullStr | Network-based identification of biomarkers for colon adenocarcinoma |
title_full_unstemmed | Network-based identification of biomarkers for colon adenocarcinoma |
title_short | Network-based identification of biomarkers for colon adenocarcinoma |
title_sort | network-based identification of biomarkers for colon adenocarcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367377/ https://www.ncbi.nlm.nih.gov/pubmed/32680494 http://dx.doi.org/10.1186/s12885-020-07157-w |
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