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Human liver organoids for disease modeling of fibrolamellar carcinoma

Fibrolamellar carcinoma (FLC) is a rare, often lethal, liver cancer affecting adolescents and young adults, for which there are no approved therapeutics. The development of therapeutics is hampered by a lack of in vitro models. Organoids have shown utility as a model system for studying many disease...

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Autores principales: Narayan, Nicole J.C., Requena, David, Lalazar, Gadi, Ramos-Espiritu, Lavoisier, Ng, Denise, Levin, Solomon, Shebl, Bassem, Wang, Ruisi, Hammond, William J., Saltsman, James A., Gehart, Helmuth, Torbenson, Michael S., Clevers, Hans, LaQuaglia, Michael P., Simon, Sanford M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9391427/
https://www.ncbi.nlm.nih.gov/pubmed/35803261
http://dx.doi.org/10.1016/j.stemcr.2022.06.003
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author Narayan, Nicole J.C.
Requena, David
Lalazar, Gadi
Ramos-Espiritu, Lavoisier
Ng, Denise
Levin, Solomon
Shebl, Bassem
Wang, Ruisi
Hammond, William J.
Saltsman, James A.
Gehart, Helmuth
Torbenson, Michael S.
Clevers, Hans
LaQuaglia, Michael P.
Simon, Sanford M.
author_facet Narayan, Nicole J.C.
Requena, David
Lalazar, Gadi
Ramos-Espiritu, Lavoisier
Ng, Denise
Levin, Solomon
Shebl, Bassem
Wang, Ruisi
Hammond, William J.
Saltsman, James A.
Gehart, Helmuth
Torbenson, Michael S.
Clevers, Hans
LaQuaglia, Michael P.
Simon, Sanford M.
author_sort Narayan, Nicole J.C.
collection PubMed
description Fibrolamellar carcinoma (FLC) is a rare, often lethal, liver cancer affecting adolescents and young adults, for which there are no approved therapeutics. The development of therapeutics is hampered by a lack of in vitro models. Organoids have shown utility as a model system for studying many diseases. In this study, tumor tissue and the adjacent non-tumor liver were obtained at the time of surgery. The tissue was dissociated and grown as organoids. We developed 21 patient-derived organoid lines: 12 from metastases, three from the liver tumor and six from adjacent non-tumor liver. These patient-derived FLC organoids recapitulate the histologic morphology, immunohistochemistry, and transcriptome of the patient tumor. Patient-derived FLC organoids were used in a preliminary high-throughput drug screen to show proof of concept for the identification of therapeutics. This model system has the potential to improve our understanding of this rare cancer and holds significant promise for drug testing and development.
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spelling pubmed-93914272022-08-21 Human liver organoids for disease modeling of fibrolamellar carcinoma Narayan, Nicole J.C. Requena, David Lalazar, Gadi Ramos-Espiritu, Lavoisier Ng, Denise Levin, Solomon Shebl, Bassem Wang, Ruisi Hammond, William J. Saltsman, James A. Gehart, Helmuth Torbenson, Michael S. Clevers, Hans LaQuaglia, Michael P. Simon, Sanford M. Stem Cell Reports Article Fibrolamellar carcinoma (FLC) is a rare, often lethal, liver cancer affecting adolescents and young adults, for which there are no approved therapeutics. The development of therapeutics is hampered by a lack of in vitro models. Organoids have shown utility as a model system for studying many diseases. In this study, tumor tissue and the adjacent non-tumor liver were obtained at the time of surgery. The tissue was dissociated and grown as organoids. We developed 21 patient-derived organoid lines: 12 from metastases, three from the liver tumor and six from adjacent non-tumor liver. These patient-derived FLC organoids recapitulate the histologic morphology, immunohistochemistry, and transcriptome of the patient tumor. Patient-derived FLC organoids were used in a preliminary high-throughput drug screen to show proof of concept for the identification of therapeutics. This model system has the potential to improve our understanding of this rare cancer and holds significant promise for drug testing and development. Elsevier 2022-07-07 /pmc/articles/PMC9391427/ /pubmed/35803261 http://dx.doi.org/10.1016/j.stemcr.2022.06.003 Text en © 2022 The Author(s) 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 Article
Narayan, Nicole J.C.
Requena, David
Lalazar, Gadi
Ramos-Espiritu, Lavoisier
Ng, Denise
Levin, Solomon
Shebl, Bassem
Wang, Ruisi
Hammond, William J.
Saltsman, James A.
Gehart, Helmuth
Torbenson, Michael S.
Clevers, Hans
LaQuaglia, Michael P.
Simon, Sanford M.
Human liver organoids for disease modeling of fibrolamellar carcinoma
title Human liver organoids for disease modeling of fibrolamellar carcinoma
title_full Human liver organoids for disease modeling of fibrolamellar carcinoma
title_fullStr Human liver organoids for disease modeling of fibrolamellar carcinoma
title_full_unstemmed Human liver organoids for disease modeling of fibrolamellar carcinoma
title_short Human liver organoids for disease modeling of fibrolamellar carcinoma
title_sort human liver organoids for disease modeling of fibrolamellar carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9391427/
https://www.ncbi.nlm.nih.gov/pubmed/35803261
http://dx.doi.org/10.1016/j.stemcr.2022.06.003
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