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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

We provide a comprehensive overview and refinement of existing protocols for hepatocellular carcinoma (HCC) organoid formation, encompassing all stages of organoid cultivation. This system serves as a valuable model for the identification of potential therapeutic targets and the assessment of drug candidate effectiveness.

Abstract

Hepatocellular carcinoma (HCC) is a highly prevalent and lethal tumor worldwide and its late discovery and lack of effective specific therapeutic agents necessitate further research into its pathogenesis and treatment. Organoids, a novel model that closely resembles native tumor tissue and can be cultured in vitro, have garnered significant interest in recent years, with numerous reports on the development of organoid models for liver cancer. In this study, we have successfully optimized the procedure and established a culture protocol that enables the formation of larger-sized HCC organoids with stable passaging and culture conditions. We have comprehensively outlined each step of the procedure, covering the entire process of HCC tissue dissociation, organoid plating, culture, passaging, cryopreservation, and resuscitation, and provided detailed precautions in this paper. These organoids exhibit genetic similarity to the original HCC tissues and can be utilized for diverse applications, including the identification of potential therapeutic targets for tumors and subsequent drug development.

Introduction

Hepatocellular carcinoma (HCC), a prevalent and extensively diverse tumor1, has garnered considerable attention within the medical community. The presence of lineage plasticity and substantial heterogeneity in HCC suggests that tumor cells originating from various patients and even distinct lesions within the same patient may manifest dissimilar molecular and phenotypic traits, thereby presenting formidable obstacles in the advancement of innovative therapeutic approaches2,3,4,5. Consequently, there is an imperative n....

Protocol

Human-biopsied tissues were obtained from the respective patient at the Affiliated Cancer Hospital and Institute of Guangzhou Medical University, and informed consent was obtained from the patients. See the Table of Materials for details about all materials, reagents, and instruments used in this protocol.

1. Establishing patient-derived HCC organoids from surgical samples

NOTE: The establishment of HCC organoids encompasses various s.......

Representative Results

Upon implementing the aforementioned procedure, the emergence of HCC organoid spheroids is typically observable within a span of 3 days (Figure 1). Figure 1A,B show the established HCC organoid, which promptly develops compact spheroids characterized by rounded edges and permeable cytosol on the initial day of establishment. During the growth of HCC organoids, the use of different concentrations of BME had different effects on the growth rate of.......

Discussion

One notable benefit of patient-derived organoid models lies in their capacity to faithfully replicate the biological characteristics of tumors, encompassing tissue structure and genomic landscape. These models demonstrate a remarkable level of accuracy and effectively mirror the heterogeneity and progression of tumors, even over extended periods of cultivation6,8,9. Through the utilization of this refined organoid culture protoc.......

Acknowledgements

This research was supported by the National Natural Science Foundation of China (82122048; 82003773; 82203380) and Guangdong Basic and Applied Basic Research Foundation (2023A1515011416).

....

Materials

NameCompanyCatalog NumberComments
[Leu15]-gastrin I humanMerckG9145
1.5 mL MicrotubesMerckAXYMCT150LC
A8301 (TGFβ inhibitor)Tocris Bioscience2939
B27 Supplement (503), minus vitamin AThermo Fisher Scientific12587010
B-27 Supplement (503), serum-freeThermo Fisher Scientific17504044
BMP7Peprotech120-03P
Cell strainer size 100 μmMerckCLS352360
CHIR99021MerckSML1046
Collagenase DMerck11088858001
Corning Costar Ultra-LowMerckCLS3473
Costar 24-well Clear Flat Bottom Ultra-Low Attachment Multiple Well Plates, Individually Wrapped, SterileCorning3473
Costar 6-well Clear Flat Bottom Ultra-Low Attachment Multiple Well Plates, Individually Wrapped, SterileCorning3471
Cultrex Organoid Harvesting SolutionR&D SYSTEMS3700-100-01Organoid harvesting solution
Cultrex Reduced Growth Factor BME, Type 2 PathClear (BME)Merck3533-005-02
DAPTMerckD5942
DexamethasoneMerckD4902
DMSOMerckC6164
DNaseIMerckDN25
Dulbecco's Modified Eagle Medium/Ham's F-12Thermo Fisher Scientific12634028Advanced DMEM/F-12
Earle’s balanced salt solution (EBSS)Thermo Fisher Scientific24010043
ForcepsN/AN/A
ForskolinTocris Bioscience1099
GlutaMAX supplementThermo Fisher Scientific35050061
HEPES, 1 MThermo Fisher Scientific15630080
Leica DM6 B Fluorescence Motorized MicroscopeLeicaN/A
N2 supplement (1003)Thermo Fisher Scientific17502048
N-acetylcysteineMerckA0737-5MG
NicotinamideMerckN0636
Nunc 15 mL Conical Sterile Polypropylene Centrifuge TubesThermo Fisher Scientific339651
Nunc 50 mL Conical Sterile Polypropylene Centrifuge TubesThermo Fisher Scientific339653
Penicillin/streptomycin (10,000 U/mL)Thermo Fisher Scientific15140122
Recombinant human EGFPeprotechAF-100-15
Recombinant human FGF10Peprotech100-26
Recombinant human FGF19Peprotech100-32
Recombinant human HGFPeprotech100-39
Recombinant human NogginPeprotech120-10C
Rho kinase inhibitor Y-27632 dihydrochlorideMerckY0503
R-spodin1-conditioned medium(Broutier et al.)N/ASecretion of cell lines
Surgical scissorsN/AN/A
Surgical specimen of tumor removed from HCC patientsAffiliated Cancer Hospital and Institute of Guangzhou Medical UniversityN/A
TNFαPeprotech315-01A
TrypLE Express Enzyme (1x), no phenol redThermo Fisher Scientific12604013Trypsin substitute
Wnt-3a-conditioned medium(Broutier et al.)N/ASecretion of cell lines

References

  1. Vogel, A., Meyer, T., Sapisochin, G., Salem, R., Saborowski, A. Hepatocellular carcinoma. Lancet. 400 (10360), 1345-1362 (2022).
  2. Craig, A. J., von Felden, J., Garcia-Lezana, T., Sarcognato, S., Villanueva, A. Tumour evolution in hepatocellular carcinoma.

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