TY - JOUR
T1 - Human liver organoids for disease modeling of fibrolamellar carcinoma
AU - Narayan, Nicole J.C.
AU - Requena, David
AU - Lalazar, Gadi
AU - Ramos-Espiritu, Lavoisier
AU - Ng, Denise
AU - Levin, Solomon
AU - Shebl, Bassem
AU - Wang, Ruisi
AU - Hammond, William J.
AU - Saltsman, James A.
AU - Gehart, Helmuth
AU - Torbenson, Michael S.
AU - Clevers, Hans
AU - LaQuaglia, Michael P.
AU - Simon, Sanford M.
N1 - Publisher Copyright:
© 2022 The Author(s)
PY - 2022/8/9
Y1 - 2022/8/9
N2 - 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.
AB - 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.
KW - fibrolamellar
KW - liver cancer
KW - pediatric cancer
UR - http://www.scopus.com/inward/record.url?scp=85135689782&partnerID=8YFLogxK
U2 - 10.1016/j.stemcr.2022.06.003
DO - 10.1016/j.stemcr.2022.06.003
M3 - Article
C2 - 35803261
AN - SCOPUS:85135689782
VL - 17
SP - 1874
EP - 1888
JO - Stem Cell Reports
JF - Stem Cell Reports
SN - 2213-6711
IS - 8
ER -