Patient-derived organoids in precision cancer medicine

被引:19
作者
Tong, Le [1 ]
Cui, Weiyingqi [2 ]
Zhang, Boya [3 ]
Fonseca, Pedro [1 ]
Zhao, Qian [3 ]
Zhang, Ping [3 ]
Xu, Beibei [4 ]
Zhang, Qisi [4 ]
Li, Zhen [4 ]
Seashore-Ludlow, Brinton [1 ]
Yang, Ying [1 ,5 ]
Si, Longlong [4 ]
Lundqvist, Andreas [1 ]
机构
[1] Karolinska Inst, Dept Oncol Pathol, Stockholm, Sweden
[2] Karolinska Inst, Chem Biol Consortium Sweden, Sci Life Lab, Stockholm, Sweden
[3] Organcare Shenzhen Biotechnol Co, Shenzhen, Peoples R China
[4] Chinese Acad Sci, Shenzhen Inst Synthet Biol, Shenzhen Inst Adv Technol, Key Lab Quantitat Synthet Biol, Shenzhen, Peoples R China
[5] Zhejiang Univ, Affiliated Hosp 4, Int Inst Med, Sch Med,Dept Resp Med, Hangzhou, Zhejiang, Peoples R China
来源
MED | 2024年 / 5卷 / 11期
基金
芬兰科学院;
关键词
LONG-TERM EXPANSION; ON-A-CHIP; TUMOR MICROENVIRONMENT; COLORECTAL-CANCER; HUMAN COLON; STEM-CELLS; PREDICTIVE BIOMARKERS; CEREBRAL ORGANOIDS; LIVING BIOBANK; MODELS;
D O I
10.1016/j.medj.2024.08.010
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Organoids are three-dimensional (3D) cultures, normally derived from stem cells, that replicate the complex structure and function of human tissues. They offer a physiologically relevant model to address important questions in cancer research. The generation of patient-derived organoids (PDOs) from various human cancers allows for deeper insights into tumor heterogeneity and spatial organization. Additionally, interrogating non-tumor stromal cells increases the relevance in studying the tumor microenvironment, thereby enhancing the relevance of PDOs in personalized medicine. PDOs mark a significant advancement in cancer research and patient care, signifying a shift toward more innovative and patient-centric approaches. This review covers aspects of PDO cultures to address the modeling of the tumor microenvironment, including extracellular matrices, air-liquid interface and microfluidic cultures, and organ-on-chip. Specifically, the role of PDOs as preclinical models in gene editing, molecular profiling, drug testing, and biomarker discovery and their potential for guiding personalized treatment in clinical practice are discussed.
引用
收藏
页码:1351 / 1377
页数:27
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