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New LncRNAs in Chronic Hepatitis C progression: from fibrosis to hepatocellular carcinoma
Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related death in the world, and about 80% of the cases are associated with hepatitis B or C. Genetic and epigenetic alterations are accumulated over decades of chronic injury and may affect the functioning of tumor suppressor genes...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303194/ https://www.ncbi.nlm.nih.gov/pubmed/32555359 http://dx.doi.org/10.1038/s41598-020-66881-2 |
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author | Ferrasi, Adriana Camargo Fernandez, Geysson Javier Grotto, Rejane Maria Tommasini Silva, Giovanni Faria Goncalves, Joao Costa, Marina C. Enguita, Francisco J. Pardini, Maria Inês de Moura Campos |
author_facet | Ferrasi, Adriana Camargo Fernandez, Geysson Javier Grotto, Rejane Maria Tommasini Silva, Giovanni Faria Goncalves, Joao Costa, Marina C. Enguita, Francisco J. Pardini, Maria Inês de Moura Campos |
author_sort | Ferrasi, Adriana Camargo |
collection | PubMed |
description | Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related death in the world, and about 80% of the cases are associated with hepatitis B or C. Genetic and epigenetic alterations are accumulated over decades of chronic injury and may affect the functioning of tumor suppressor genes and protooncogenes. Studies have evidenced the role of Long non-coding RNAs (LncRNA) with oncogenic or tumor suppressor activities, suggesting a great potential in the treatment, diagnosis or indicator of prognosis in cancer. In this context, the aim of this study was to evaluate the global expression profile lncRNA in hepatic tissue samples with different stages of fibrosis associated with chronic hepatitis C, HCC and normal liver, in order to identify new lncRNAs that could contribute to study the progression of hepatic fibrosis to HCC associated with chronic hepatitis C. RNA-Seq was performed on Illumina NextSeq platform to identify lncRNAs expressed differently in 15 patients with chronic hepatitis C, three patients with HCC and three normal liver specimens. When the pathological tissues (fibrosis and carcinoma) were compared to normal hepatic tissue, were identified 2, 6 e 34 differentially expressed lncRNAs in moderate fibrosis, advanced fibrosis and HCC, respectively. The carcinoma group had the highest proportion of differentially expressed lncRNA (34) and of these, 29 were exclusive in this type of tissue. A heat map of the deregulated lncRNA revealed different expression patterns along the progression of fibrosis to HCC. The results showed the deregulation of some lncRNA already classified as tumor suppressors in HCC and other cancers, as well as some unpublished lncRNA whose function is unknown. Some of these lncRNAs are dysregulated since the early stages of liver injury in patients with hepatitis C, others overexpressed only in tumor tissue, indicating themselves as candidates of markers of fibrosis progression or tumor, with potential clinical applications in prognosis as well as a therapeutic target. Although there are already studies on lncRNA in hepatocellular carcinoma, this is the first study conducted in samples exclusively of HCV-related liver and HCV HCC. |
format | Online Article Text |
id | pubmed-7303194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73031942020-06-22 New LncRNAs in Chronic Hepatitis C progression: from fibrosis to hepatocellular carcinoma Ferrasi, Adriana Camargo Fernandez, Geysson Javier Grotto, Rejane Maria Tommasini Silva, Giovanni Faria Goncalves, Joao Costa, Marina C. Enguita, Francisco J. Pardini, Maria Inês de Moura Campos Sci Rep Article Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related death in the world, and about 80% of the cases are associated with hepatitis B or C. Genetic and epigenetic alterations are accumulated over decades of chronic injury and may affect the functioning of tumor suppressor genes and protooncogenes. Studies have evidenced the role of Long non-coding RNAs (LncRNA) with oncogenic or tumor suppressor activities, suggesting a great potential in the treatment, diagnosis or indicator of prognosis in cancer. In this context, the aim of this study was to evaluate the global expression profile lncRNA in hepatic tissue samples with different stages of fibrosis associated with chronic hepatitis C, HCC and normal liver, in order to identify new lncRNAs that could contribute to study the progression of hepatic fibrosis to HCC associated with chronic hepatitis C. RNA-Seq was performed on Illumina NextSeq platform to identify lncRNAs expressed differently in 15 patients with chronic hepatitis C, three patients with HCC and three normal liver specimens. When the pathological tissues (fibrosis and carcinoma) were compared to normal hepatic tissue, were identified 2, 6 e 34 differentially expressed lncRNAs in moderate fibrosis, advanced fibrosis and HCC, respectively. The carcinoma group had the highest proportion of differentially expressed lncRNA (34) and of these, 29 were exclusive in this type of tissue. A heat map of the deregulated lncRNA revealed different expression patterns along the progression of fibrosis to HCC. The results showed the deregulation of some lncRNA already classified as tumor suppressors in HCC and other cancers, as well as some unpublished lncRNA whose function is unknown. Some of these lncRNAs are dysregulated since the early stages of liver injury in patients with hepatitis C, others overexpressed only in tumor tissue, indicating themselves as candidates of markers of fibrosis progression or tumor, with potential clinical applications in prognosis as well as a therapeutic target. Although there are already studies on lncRNA in hepatocellular carcinoma, this is the first study conducted in samples exclusively of HCV-related liver and HCV HCC. Nature Publishing Group UK 2020-06-18 /pmc/articles/PMC7303194/ /pubmed/32555359 http://dx.doi.org/10.1038/s41598-020-66881-2 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 Ferrasi, Adriana Camargo Fernandez, Geysson Javier Grotto, Rejane Maria Tommasini Silva, Giovanni Faria Goncalves, Joao Costa, Marina C. Enguita, Francisco J. Pardini, Maria Inês de Moura Campos New LncRNAs in Chronic Hepatitis C progression: from fibrosis to hepatocellular carcinoma |
title | New LncRNAs in Chronic Hepatitis C progression: from fibrosis to hepatocellular carcinoma |
title_full | New LncRNAs in Chronic Hepatitis C progression: from fibrosis to hepatocellular carcinoma |
title_fullStr | New LncRNAs in Chronic Hepatitis C progression: from fibrosis to hepatocellular carcinoma |
title_full_unstemmed | New LncRNAs in Chronic Hepatitis C progression: from fibrosis to hepatocellular carcinoma |
title_short | New LncRNAs in Chronic Hepatitis C progression: from fibrosis to hepatocellular carcinoma |
title_sort | new lncrnas in chronic hepatitis c progression: from fibrosis to hepatocellular carcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303194/ https://www.ncbi.nlm.nih.gov/pubmed/32555359 http://dx.doi.org/10.1038/s41598-020-66881-2 |
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