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Identification of a protein signature for predicting overall survival of hepatocellular carcinoma: a study based on data mining
BACKGROUND: Hepatocellular carcinoma (HCC), is the fifth most common cancer in the world and the second most common cause of cancer-related deaths. Over 500,000 new HCC cases are diagnosed each year. Combining advanced genomic analysis with proteomic characterization not only has great potential in...
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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/PMC7398333/ https://www.ncbi.nlm.nih.gov/pubmed/32746792 http://dx.doi.org/10.1186/s12885-020-07229-x |
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author | Wu, Zeng-hong Yang, Dong-liang |
author_facet | Wu, Zeng-hong Yang, Dong-liang |
author_sort | Wu, Zeng-hong |
collection | PubMed |
description | BACKGROUND: Hepatocellular carcinoma (HCC), is the fifth most common cancer in the world and the second most common cause of cancer-related deaths. Over 500,000 new HCC cases are diagnosed each year. Combining advanced genomic analysis with proteomic characterization not only has great potential in the discovery of useful biomarkers but also drives the development of new diagnostic methods. METHODS: This study obtained proteomic data from Clinical Proteomic Tumor Analysis Consortium (CPTAC) and validated in The Cancer Proteome Atlas (TCPA) and TCGA dataset to identify HCC biomarkers and the dysfunctional of proteogenomics. RESULTS: The CPTAC database contained data for 159 patients diagnosed with Hepatitis-B related HCC and 422 differentially expressed proteins (112 upregulated and 310 downregulated proteins). Restricting our analysis to the intersection in survival-related proteins between CPTAC and TCPA database revealed four coverage survival-related proteins including PCNA, MSH6, CDK1, and ASNS. CONCLUSION: This study established a novel protein signature for HCC prognosis prediction using data retrieved from online databases. However, the signatures need to be verified using independent cohorts and functional experiments. |
format | Online Article Text |
id | pubmed-7398333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73983332020-08-06 Identification of a protein signature for predicting overall survival of hepatocellular carcinoma: a study based on data mining Wu, Zeng-hong Yang, Dong-liang BMC Cancer Research Article BACKGROUND: Hepatocellular carcinoma (HCC), is the fifth most common cancer in the world and the second most common cause of cancer-related deaths. Over 500,000 new HCC cases are diagnosed each year. Combining advanced genomic analysis with proteomic characterization not only has great potential in the discovery of useful biomarkers but also drives the development of new diagnostic methods. METHODS: This study obtained proteomic data from Clinical Proteomic Tumor Analysis Consortium (CPTAC) and validated in The Cancer Proteome Atlas (TCPA) and TCGA dataset to identify HCC biomarkers and the dysfunctional of proteogenomics. RESULTS: The CPTAC database contained data for 159 patients diagnosed with Hepatitis-B related HCC and 422 differentially expressed proteins (112 upregulated and 310 downregulated proteins). Restricting our analysis to the intersection in survival-related proteins between CPTAC and TCPA database revealed four coverage survival-related proteins including PCNA, MSH6, CDK1, and ASNS. CONCLUSION: This study established a novel protein signature for HCC prognosis prediction using data retrieved from online databases. However, the signatures need to be verified using independent cohorts and functional experiments. BioMed Central 2020-08-03 /pmc/articles/PMC7398333/ /pubmed/32746792 http://dx.doi.org/10.1186/s12885-020-07229-x 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 Wu, Zeng-hong Yang, Dong-liang Identification of a protein signature for predicting overall survival of hepatocellular carcinoma: a study based on data mining |
title | Identification of a protein signature for predicting overall survival of hepatocellular carcinoma: a study based on data mining |
title_full | Identification of a protein signature for predicting overall survival of hepatocellular carcinoma: a study based on data mining |
title_fullStr | Identification of a protein signature for predicting overall survival of hepatocellular carcinoma: a study based on data mining |
title_full_unstemmed | Identification of a protein signature for predicting overall survival of hepatocellular carcinoma: a study based on data mining |
title_short | Identification of a protein signature for predicting overall survival of hepatocellular carcinoma: a study based on data mining |
title_sort | identification of a protein signature for predicting overall survival of hepatocellular carcinoma: a study based on data mining |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398333/ https://www.ncbi.nlm.nih.gov/pubmed/32746792 http://dx.doi.org/10.1186/s12885-020-07229-x |
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