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Non coding RNA analysis in fibrolamellar hepatocellular carcinoma
Fibrolamellar hepatocellular carcinoma (FLC) is a rare primary liver cancer found in adolescents and young adults without underlying liver disease. A deletion of ~400 kD has been found in one copy of chromosome 19 in the tumor tissue of all patients tested. This produces a fusion of the genes DNAJB1...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828204/ https://www.ncbi.nlm.nih.gov/pubmed/29535801 http://dx.doi.org/10.18632/oncotarget.23325 |
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author | Farber, Benjamin A. Lalazar, Gadi Simon, Elana P. Hammond, William J. Requena, David Bhanot, Umesh K. La Quaglia, Michael P. Simon, Sanford M. |
author_facet | Farber, Benjamin A. Lalazar, Gadi Simon, Elana P. Hammond, William J. Requena, David Bhanot, Umesh K. La Quaglia, Michael P. Simon, Sanford M. |
author_sort | Farber, Benjamin A. |
collection | PubMed |
description | Fibrolamellar hepatocellular carcinoma (FLC) is a rare primary liver cancer found in adolescents and young adults without underlying liver disease. A deletion of ~400 kD has been found in one copy of chromosome 19 in the tumor tissue of all patients tested. This produces a fusion of the genes DNAJB1 and PRKACA which, in turn, produces a chimeric transcript and protein. Transcriptomic analysis of the tumor has shown upregulation of various oncologically relevant pathways, including EGF/ErbB, Aurora Kinase A, pak21 and wnt. To explore other factors that may contribute to oncogenesis, we examined the microRNA (miRNA) and long non-coding RNA (lncRNA) expression in FLC. The non-coding RNA expression profile in tumor tissue samples is distinctly different from the adjacent normal liver and from other liver tumors. Furthermore, miRZip knock down or over expression of certain miRNAs led to changes in the levels of coding genes that recapitulated changes observed in FLC, suggesting mechanistically that the changes in the cellular levels of miRNA are not merely correlative. Thus, in addition to serving as diagnostic tools for FLC, non-coding RNAs may serve as therapeutic targets. |
format | Online Article Text |
id | pubmed-5828204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-58282042018-03-13 Non coding RNA analysis in fibrolamellar hepatocellular carcinoma Farber, Benjamin A. Lalazar, Gadi Simon, Elana P. Hammond, William J. Requena, David Bhanot, Umesh K. La Quaglia, Michael P. Simon, Sanford M. Oncotarget Research Paper Fibrolamellar hepatocellular carcinoma (FLC) is a rare primary liver cancer found in adolescents and young adults without underlying liver disease. A deletion of ~400 kD has been found in one copy of chromosome 19 in the tumor tissue of all patients tested. This produces a fusion of the genes DNAJB1 and PRKACA which, in turn, produces a chimeric transcript and protein. Transcriptomic analysis of the tumor has shown upregulation of various oncologically relevant pathways, including EGF/ErbB, Aurora Kinase A, pak21 and wnt. To explore other factors that may contribute to oncogenesis, we examined the microRNA (miRNA) and long non-coding RNA (lncRNA) expression in FLC. The non-coding RNA expression profile in tumor tissue samples is distinctly different from the adjacent normal liver and from other liver tumors. Furthermore, miRZip knock down or over expression of certain miRNAs led to changes in the levels of coding genes that recapitulated changes observed in FLC, suggesting mechanistically that the changes in the cellular levels of miRNA are not merely correlative. Thus, in addition to serving as diagnostic tools for FLC, non-coding RNAs may serve as therapeutic targets. Impact Journals LLC 2017-12-15 /pmc/articles/PMC5828204/ /pubmed/29535801 http://dx.doi.org/10.18632/oncotarget.23325 Text en Copyright: © 2018 Farber et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Farber, Benjamin A. Lalazar, Gadi Simon, Elana P. Hammond, William J. Requena, David Bhanot, Umesh K. La Quaglia, Michael P. Simon, Sanford M. Non coding RNA analysis in fibrolamellar hepatocellular carcinoma |
title | Non coding RNA analysis in fibrolamellar hepatocellular carcinoma |
title_full | Non coding RNA analysis in fibrolamellar hepatocellular carcinoma |
title_fullStr | Non coding RNA analysis in fibrolamellar hepatocellular carcinoma |
title_full_unstemmed | Non coding RNA analysis in fibrolamellar hepatocellular carcinoma |
title_short | Non coding RNA analysis in fibrolamellar hepatocellular carcinoma |
title_sort | non coding rna analysis in fibrolamellar hepatocellular carcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828204/ https://www.ncbi.nlm.nih.gov/pubmed/29535801 http://dx.doi.org/10.18632/oncotarget.23325 |
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