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* These authors contributed equally
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.
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.
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....
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.......
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.......
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.......
This research was supported by the National Natural Science Foundation of China (82122048; 82003773; 82203380) and Guangdong Basic and Applied Basic Research Foundation (2023A1515011416).
....Name | Company | Catalog Number | Comments |
[Leu15]-gastrin I human | Merck | G9145 | |
1.5 mL Microtubes | Merck | AXYMCT150LC | |
A8301 (TGFβ inhibitor) | Tocris Bioscience | 2939 | |
B27 Supplement (503), minus vitamin A | Thermo Fisher Scientific | 12587010 | |
B-27 Supplement (503), serum-free | Thermo Fisher Scientific | 17504044 | |
BMP7 | Peprotech | 120-03P | |
Cell strainer size 100 μm | Merck | CLS352360 | |
CHIR99021 | Merck | SML1046 | |
Collagenase D | Merck | 11088858001 | |
Corning Costar Ultra-Low | Merck | CLS3473 | |
Costar 24-well Clear Flat Bottom Ultra-Low Attachment Multiple Well Plates, Individually Wrapped, Sterile | Corning | 3473 | |
Costar 6-well Clear Flat Bottom Ultra-Low Attachment Multiple Well Plates, Individually Wrapped, Sterile | Corning | 3471 | |
Cultrex Organoid Harvesting Solution | R&D SYSTEMS | 3700-100-01 | Organoid harvesting solution |
Cultrex Reduced Growth Factor BME, Type 2 PathClear (BME) | Merck | 3533-005-02 | |
DAPT | Merck | D5942 | |
Dexamethasone | Merck | D4902 | |
DMSO | Merck | C6164 | |
DNaseI | Merck | DN25 | |
Dulbecco's Modified Eagle Medium/Ham's F-12 | Thermo Fisher Scientific | 12634028 | Advanced DMEM/F-12 |
Earle’s balanced salt solution (EBSS) | Thermo Fisher Scientific | 24010043 | |
Forceps | N/A | N/A | |
Forskolin | Tocris Bioscience | 1099 | |
GlutaMAX supplement | Thermo Fisher Scientific | 35050061 | |
HEPES, 1 M | Thermo Fisher Scientific | 15630080 | |
Leica DM6 B Fluorescence Motorized Microscope | Leica | N/A | |
N2 supplement (1003) | Thermo Fisher Scientific | 17502048 | |
N-acetylcysteine | Merck | A0737-5MG | |
Nicotinamide | Merck | N0636 | |
Nunc 15 mL Conical Sterile Polypropylene Centrifuge Tubes | Thermo Fisher Scientific | 339651 | |
Nunc 50 mL Conical Sterile Polypropylene Centrifuge Tubes | Thermo Fisher Scientific | 339653 | |
Penicillin/streptomycin (10,000 U/mL) | Thermo Fisher Scientific | 15140122 | |
Recombinant human EGF | Peprotech | AF-100-15 | |
Recombinant human FGF10 | Peprotech | 100-26 | |
Recombinant human FGF19 | Peprotech | 100-32 | |
Recombinant human HGF | Peprotech | 100-39 | |
Recombinant human Noggin | Peprotech | 120-10C | |
Rho kinase inhibitor Y-27632 dihydrochloride | Merck | Y0503 | |
R-spodin1-conditioned medium | (Broutier et al.) | N/A | Secretion of cell lines |
Surgical scissors | N/A | N/A | |
Surgical specimen of tumor removed from HCC patients | Affiliated Cancer Hospital and Institute of Guangzhou Medical University | N/A | |
TNFα | Peprotech | 315-01A | |
TrypLE Express Enzyme (1x), no phenol red | Thermo Fisher Scientific | 12604013 | Trypsin substitute |
Wnt-3a-conditioned medium | (Broutier et al.) | N/A | Secretion of cell lines |
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