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Table 1 Organoid models of liver cancer from different sources and their applications

From: Organoid as a promising tool for primary liver cancer research: a comprehensive review

Classification

Published Year

Cell/Tissue

Materials/Consumables

Application

Ref

Cell

2015

HEPG2, HCT116

HA hydrogel-coated microcarrier bead

Modeling tumor growth in vitro.

Becoming metastatic tumor models.

Drug screening.

Understanding the effects of potential drug candidates on normal tissues surrounding tumors.

[71]

2017

HCCLM3, Hep3B, HUVEC

Human primary fibroblasts

Matrigel

Investigating the role of non-stromal cells in the cellular composition of HCC organoids.

Increasing epithelial-mesenchymal transition and tumor malignancy.

Increasing neovascularization.

[76]

2018

WI38, LX2, HUVEC

Primary hepatocellular carcinoma cells from HBV-infected patients: AMC-H1, AMC-H2

96-well round bottom ULA microplates

Comparing anticancer drug sensitivity in different culture methods.

Optimizing the treatment of HCC.

[78]

2021

iPSC-EC, iPSC-MC, Huh7-Luci

Ibidi culture-insert 2 well system

Generation of animal models of in situ cancer.

Studying HCC tumor development under liver fibrosis TME.

[77]

Mouse liver tumor

2019

DEN-induced liver tumors

Matrigel

Initiating tumor formation in mouse xenografts.

Drug evaluation.

Promoting the development of targeted therapies for TIC.

[79]

2023

Tp53 and Pten double mutation-induced liver tumors

Matrigel

Assessing radiation sensitivity.

[80]

Patient-derived liver tumor

2017

Patient-derived PLC specimens

BME2

Constructing liver cancer organoids.

Identifying potential prognostic biomarkers for primary liver cancer.

Identifying patient-specific drug sensitivity.

Searching for potential targets in primary liver cancer.

[19]

2018

Tumor needle biopsies of liver cancers

BME2

Initiating tumor formation in mouse xenografts.

Understanding tumor heterogeneity.

Drug reaction.

Biobank.

[40]

2019

Patient-derived PLC specimens

Matrigel

Understanding intra-tumor heterogeneity.

Understanding inter-patient drug response heterogeneity.

Drug screening.

[41]

2020

Patient-derived HB specimens

BME2

Modeling HB disease.

Drug screening.

[86]

2022

Patient-derived PLC specimens

Matrigel

Drug screening.

Studying sorafenib resistance in HCC organoids.

Exploring signaling pathways that inhibit HCC organoid growth.

[82]

2022

Patient-derived FLC specimens

BME2

Modeling FLC disease.

Drug screening.

[85]

Genetic engineering

2019

hiHep

24-well Kuraray ultra-low attachment plate

Simulation of liver cancer initiation.

Performing lineage switching of hepatocytes.

Introducing multiple mutations to mimic liver cancer progression.

[92]

2023

Human fetal hepatocyte-like organoids

Matrigel

Modeling FLC disease.

Investigating molecular pathogenesis.

[96]

  1. BME2, basement membrane extract 2; DEN, diethylinitrosamine; EC, endothelial cell; FLC, fribolamellar carcinoma; HA, hyaluronic acid; HUVEC, human umbilical vein endothelial cell; HCC, hepatocellular carcinoma; HB, hepatoblastoma; iPSC, induced pluripotent stem cell; Luci, luciferase-expressing; MC, mesenchymal cell; PLC, primary liver cancer; TME, tumor microenvironment; TIC, tumor-initiating cell; ULA, ultra-low attachment