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Model of fibrolamellar hepatocellular carcinomas reveals striking enrichment in cancer stem cells

The aetiology of human fibrolamellar hepatocellular carcinomas (hFL-HCCs), cancers occurring increasingly in children to young adults, is poorly understood. We present a transplantable tumour line, maintained in immune-compromised mice, and validate it as a bona fide model of hFL-HCCs by multiple me...

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Autores principales: Oikawa, Tsunekazu, Wauthier, Eliane, Dinh, Timothy A., Selitsky, Sara R., Reyna-Neyra, Andrea, Carpino, Guido, Levine, Ronald, Cardinale, Vincenzo, Klimstra, David, Gaudio, Eugenio, Alvaro, Domenico, Carrasco, Nancy, Sethupathy, Praveen, Reid, Lola M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600730/
https://www.ncbi.nlm.nih.gov/pubmed/26437858
http://dx.doi.org/10.1038/ncomms9070
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author Oikawa, Tsunekazu
Wauthier, Eliane
Dinh, Timothy A.
Selitsky, Sara R.
Reyna-Neyra, Andrea
Carpino, Guido
Levine, Ronald
Cardinale, Vincenzo
Klimstra, David
Gaudio, Eugenio
Alvaro, Domenico
Carrasco, Nancy
Sethupathy, Praveen
Reid, Lola M.
author_facet Oikawa, Tsunekazu
Wauthier, Eliane
Dinh, Timothy A.
Selitsky, Sara R.
Reyna-Neyra, Andrea
Carpino, Guido
Levine, Ronald
Cardinale, Vincenzo
Klimstra, David
Gaudio, Eugenio
Alvaro, Domenico
Carrasco, Nancy
Sethupathy, Praveen
Reid, Lola M.
author_sort Oikawa, Tsunekazu
collection PubMed
description The aetiology of human fibrolamellar hepatocellular carcinomas (hFL-HCCs), cancers occurring increasingly in children to young adults, is poorly understood. We present a transplantable tumour line, maintained in immune-compromised mice, and validate it as a bona fide model of hFL-HCCs by multiple methods. RNA-seq analysis confirms the presence of a fusion transcript (DNAJB1-PRKACA) characteristic of hFL-HCC tumours. The hFL-HCC tumour line is highly enriched for cancer stem cells as indicated by limited dilution tumourigenicity assays, spheroid formation and flow cytometry. Immunohistochemistry on the hFL-HCC model, with parallel studies on 27 primary hFL-HCC tumours, provides robust evidence for expression of endodermal stem cell traits. Transcriptomic analyses of the tumour line and of multiple, normal hepatic lineage stages reveal a gene signature for hFL-HCCs closely resembling that of biliary tree stem cells—newly discovered precursors for liver and pancreas. This model offers unprecedented opportunities to investigate mechanisms underlying hFL-HCCs pathogenesis and potential therapies.
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spelling pubmed-46007302015-10-21 Model of fibrolamellar hepatocellular carcinomas reveals striking enrichment in cancer stem cells Oikawa, Tsunekazu Wauthier, Eliane Dinh, Timothy A. Selitsky, Sara R. Reyna-Neyra, Andrea Carpino, Guido Levine, Ronald Cardinale, Vincenzo Klimstra, David Gaudio, Eugenio Alvaro, Domenico Carrasco, Nancy Sethupathy, Praveen Reid, Lola M. Nat Commun Article The aetiology of human fibrolamellar hepatocellular carcinomas (hFL-HCCs), cancers occurring increasingly in children to young adults, is poorly understood. We present a transplantable tumour line, maintained in immune-compromised mice, and validate it as a bona fide model of hFL-HCCs by multiple methods. RNA-seq analysis confirms the presence of a fusion transcript (DNAJB1-PRKACA) characteristic of hFL-HCC tumours. The hFL-HCC tumour line is highly enriched for cancer stem cells as indicated by limited dilution tumourigenicity assays, spheroid formation and flow cytometry. Immunohistochemistry on the hFL-HCC model, with parallel studies on 27 primary hFL-HCC tumours, provides robust evidence for expression of endodermal stem cell traits. Transcriptomic analyses of the tumour line and of multiple, normal hepatic lineage stages reveal a gene signature for hFL-HCCs closely resembling that of biliary tree stem cells—newly discovered precursors for liver and pancreas. This model offers unprecedented opportunities to investigate mechanisms underlying hFL-HCCs pathogenesis and potential therapies. Nature Pub. Group 2015-10-06 /pmc/articles/PMC4600730/ /pubmed/26437858 http://dx.doi.org/10.1038/ncomms9070 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Oikawa, Tsunekazu
Wauthier, Eliane
Dinh, Timothy A.
Selitsky, Sara R.
Reyna-Neyra, Andrea
Carpino, Guido
Levine, Ronald
Cardinale, Vincenzo
Klimstra, David
Gaudio, Eugenio
Alvaro, Domenico
Carrasco, Nancy
Sethupathy, Praveen
Reid, Lola M.
Model of fibrolamellar hepatocellular carcinomas reveals striking enrichment in cancer stem cells
title Model of fibrolamellar hepatocellular carcinomas reveals striking enrichment in cancer stem cells
title_full Model of fibrolamellar hepatocellular carcinomas reveals striking enrichment in cancer stem cells
title_fullStr Model of fibrolamellar hepatocellular carcinomas reveals striking enrichment in cancer stem cells
title_full_unstemmed Model of fibrolamellar hepatocellular carcinomas reveals striking enrichment in cancer stem cells
title_short Model of fibrolamellar hepatocellular carcinomas reveals striking enrichment in cancer stem cells
title_sort model of fibrolamellar hepatocellular carcinomas reveals striking enrichment in cancer stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600730/
https://www.ncbi.nlm.nih.gov/pubmed/26437858
http://dx.doi.org/10.1038/ncomms9070
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