Abstract
In recent years, the rapid emergence of 3D organoid technology has garnered significant attention from researchers. These miniature models accurately replicate the structure and function of human tissues and organs, offering more physiologically relevant platforms for cancer research. These intricate 3D structures not only serve as promising models for studying human cancer, but also significantly contribute to the advancement of various potential applications in the field of cancer research. To date, organoids have been efficiently constructed from both normal and malignant tissues originating from patients. Using such bioengineering platforms, simulations of infections and cancer processes, mutations and carcinogenesis can be achieved, and organoid technology is also expected to facilitate drug testing and personalized therapies. In conclusion, regenerative medicine has the potential to enhance organoid technology and current transplantation treatments by utilizing genetically identical healthy organoids as substitutes for irreversibly deteriorating diseased organs. This review explored the evolution of cancer organoids and emphasized the significant role these models play in fundamental research and the advancement of personalized medicine in oncology.
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Data Availability
All required data included in text and supplementary. Any further any formation required is available with the corresponding author.
Code Availability
All required code included in text and supplementary.
Abbreviations
- MRA:
-
Microraft array
- HCS:
-
High-content screening
- CF:
-
Cystic fibrosis
- ESCs:
-
Embryonic stem cells
- iPSC:
-
Induced pluripotent stem cells
- Rb:
-
Retinoblastoma
- PSCs:
-
Pluripotent stem cells
- hPSCs:
-
Human pluripotent stem cells
- SAM:
-
S-adenosylmethionine
- PM:
-
Paraxial mesoderm
- WOI:
-
Window-of-implantation
- CRC:
-
Colorectal cancer
- PDOs:
-
Patient-derived organoids
- OC:
-
Ovarian cancer
- HGSOC:
-
High-grade serous ovarian cancer
- PDAC:
-
Pancreatic ductal adenocarcinoma
- PRMT5:
-
Protein arginine methyltransferase gene 5
- PDXs:
-
Patient-derived xenografts
- DLA:
-
Diagnostic leukapheresis
- CTC:
-
Circulating tumor cell
- NSCLC:
-
Non-small cell lung cancer
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Acknowledgements
This work was supported by Hebei Medical University and funded by National Natural Science Foundation of China (No. 81971474, 8197061369 and 82201953), General Program of China Postdoctoral Science Foundation (No. 2021M701036), Hebei Key R&D Program Project Special Project for the Construction of Beijing-Tianjin-Hebei Collaborative Innovation Community (No. 22347702D), and Key Project of Natural Science Foundation of Hebei Province (C2021206011).
Funding
The work was supported by grants from the National Natural Science Foundation of China (No. 81971474, 8197061369 and 82201953), General Program of China Postdoctoral Science Foundation (No. 2021M701036), Hebei Key R&D Program Project Special Project for the Construction of Beijing-Tianjin-Hebei Collaborative Innovation Community (No. 22347702D), and Key Project of Natural Science Foundation of Hebei Province (C2021206011).
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YJY performed the selection of literature, drafted the manuscript, and prepared the figures. YJY, JLC, YJK, and ZJG collected the related references. YH and YJY carried out the design of this review and revised the manuscript. All authors contributed to this manuscript. All authors read and approved the final manuscript.
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Yang, Y., Kong, Y., Cui, J. et al. Advances and Applications of Cancer Organoids in Drug Screening and Personalized Medicine. Stem Cell Rev and Rep (2024). https://doi.org/10.1007/s12015-024-10714-6
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DOI: https://doi.org/10.1007/s12015-024-10714-6