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Identification of potential microRNA groups for the diagnosis of hepatocellular carcinoma (HCC) using microarray datasets and bioinformatics tools
Hepatocellular carcinoma (HCC) is the most common primary liver malignancy and the third cause of cancer-related death worldwide. Potential microRNAs have been reported as biomarkers for early detection of HCC as well as novel molecular targets for HCC treatment. Various tissue expression profiles o...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8873536/ https://www.ncbi.nlm.nih.gov/pubmed/35243101 http://dx.doi.org/10.1016/j.heliyon.2022.e08987 |
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author | Dat, Vo Hoang Xuan Nhung, Bui Thi Huyen Chau, Nguyen Ngoc Bao Cuong, Pham Hung Hieu, Vo Duc Linh, Nguyen Thi Minh Quoc, Nguyen Bao |
author_facet | Dat, Vo Hoang Xuan Nhung, Bui Thi Huyen Chau, Nguyen Ngoc Bao Cuong, Pham Hung Hieu, Vo Duc Linh, Nguyen Thi Minh Quoc, Nguyen Bao |
author_sort | Dat, Vo Hoang Xuan |
collection | PubMed |
description | Hepatocellular carcinoma (HCC) is the most common primary liver malignancy and the third cause of cancer-related death worldwide. Potential microRNAs have been reported as biomarkers for early detection of HCC as well as novel molecular targets for HCC treatment. Various tissue expression profiles of miRNAs using three microarray datasets from groups in Asia (2), Europe, America (GSE147892, GSE21362, GSE74618, GSE40744) and multiple bioinformatics tools were integrated to determine the most significant miRNA groups to assist in the diagnosis of HCC. Statistical analyses identified at least 30 miRNAs with 17 up-regulated and 13 down-regulated in HCC-related tumor tissues. All the miRNAs also showed relevance to the hallmarks of cancer such as cell proliferation, invasion, metastasis, angiogenesis, metabolism, epithelial-mesenchymal transition and apoptosis. Expression levels of miRNAs observed in the European group showed up-regulation at 5–37% compared to both Asian and American groups. Interestingly, four miRNAs divided into two groups as miR-182-5p/miR-1269a and miR-199a/miR-422a were the most promising for diagnosis of HCC patients from healthy controls, with AUC values of 0.902 and 0.892, respectively. Results provided evidence of the correlation between potential miRNAs and HCC that could be useful for disease diagnosis based on in-depth analyses of large case numbers and cohort studies. |
format | Online Article Text |
id | pubmed-8873536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-88735362022-03-02 Identification of potential microRNA groups for the diagnosis of hepatocellular carcinoma (HCC) using microarray datasets and bioinformatics tools Dat, Vo Hoang Xuan Nhung, Bui Thi Huyen Chau, Nguyen Ngoc Bao Cuong, Pham Hung Hieu, Vo Duc Linh, Nguyen Thi Minh Quoc, Nguyen Bao Heliyon Research Article Hepatocellular carcinoma (HCC) is the most common primary liver malignancy and the third cause of cancer-related death worldwide. Potential microRNAs have been reported as biomarkers for early detection of HCC as well as novel molecular targets for HCC treatment. Various tissue expression profiles of miRNAs using three microarray datasets from groups in Asia (2), Europe, America (GSE147892, GSE21362, GSE74618, GSE40744) and multiple bioinformatics tools were integrated to determine the most significant miRNA groups to assist in the diagnosis of HCC. Statistical analyses identified at least 30 miRNAs with 17 up-regulated and 13 down-regulated in HCC-related tumor tissues. All the miRNAs also showed relevance to the hallmarks of cancer such as cell proliferation, invasion, metastasis, angiogenesis, metabolism, epithelial-mesenchymal transition and apoptosis. Expression levels of miRNAs observed in the European group showed up-regulation at 5–37% compared to both Asian and American groups. Interestingly, four miRNAs divided into two groups as miR-182-5p/miR-1269a and miR-199a/miR-422a were the most promising for diagnosis of HCC patients from healthy controls, with AUC values of 0.902 and 0.892, respectively. Results provided evidence of the correlation between potential miRNAs and HCC that could be useful for disease diagnosis based on in-depth analyses of large case numbers and cohort studies. Elsevier 2022-02-21 /pmc/articles/PMC8873536/ /pubmed/35243101 http://dx.doi.org/10.1016/j.heliyon.2022.e08987 Text en © 2022 Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Dat, Vo Hoang Xuan Nhung, Bui Thi Huyen Chau, Nguyen Ngoc Bao Cuong, Pham Hung Hieu, Vo Duc Linh, Nguyen Thi Minh Quoc, Nguyen Bao Identification of potential microRNA groups for the diagnosis of hepatocellular carcinoma (HCC) using microarray datasets and bioinformatics tools |
title | Identification of potential microRNA groups for the diagnosis of hepatocellular carcinoma (HCC) using microarray datasets and bioinformatics tools |
title_full | Identification of potential microRNA groups for the diagnosis of hepatocellular carcinoma (HCC) using microarray datasets and bioinformatics tools |
title_fullStr | Identification of potential microRNA groups for the diagnosis of hepatocellular carcinoma (HCC) using microarray datasets and bioinformatics tools |
title_full_unstemmed | Identification of potential microRNA groups for the diagnosis of hepatocellular carcinoma (HCC) using microarray datasets and bioinformatics tools |
title_short | Identification of potential microRNA groups for the diagnosis of hepatocellular carcinoma (HCC) using microarray datasets and bioinformatics tools |
title_sort | identification of potential microrna groups for the diagnosis of hepatocellular carcinoma (hcc) using microarray datasets and bioinformatics tools |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8873536/ https://www.ncbi.nlm.nih.gov/pubmed/35243101 http://dx.doi.org/10.1016/j.heliyon.2022.e08987 |
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