Promises and challenges of organoid-guided precision medicine

被引:98
作者
Bose, Shree [1 ]
Clevers, Hans [2 ,3 ,4 ]
Shen, Xiling [1 ]
机构
[1] Duke Univ, Pratt Sch Engn, Dept Biomed Engn, Durham, NC 27705 USA
[2] Princess Maxima Ctr Pediat Oncol, Heidelberglaan 25, NL-3584 CS Utrecht, Netherlands
[3] Royal Netherlands Acad Arts & Sci KNAW, Hubrecht Inst, Oncode, Uppsalalaan 8, NL-3584 CT Utrecht, Netherlands
[4] Univ Med Ctr UMC Utrecht, Oncode, Uppsalalaan 8, NL-3584 CT Utrecht, Netherlands
来源
MED | 2021年 / 2卷 / 09期
关键词
STEM-CELL; IN-VITRO; CANCER ORGANOIDS; PROSTATE-CANCER; HUMAN COLON; DISEASE; BIOBANK; MODEL; MUTATIONS; COMPONENTS;
D O I
10.1016/j.medj.2021.08.005
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 self-organizing, expanding 3D cultures derived from stem cells. Using tissue derived from patients, these miniaturized models recapitulate various aspects of patient physiology and disease phenotypes, including genetic profiles and drug sensitivities. As such, patient-derived organoid (PDO) platforms provide an unprecedented opportunity for improving preclinical drug discovery, clinical trial validation, and, ultimately, patient care. Here, we review the evolution and scope of organoid technology, highlight recent encouraging results using PDOs as potential patient "avatars"to predict drug response and outcomes, and discuss critical parameters for widespread clinical adoption. These include improvements in assay speed, reproducibility, standardization, and automation, which are necessary to realize the translational potential of PDOs as clinical tools. The multiple entry points where PDOs may contribute valuable insights in drug discovery and lessen the risks associated with clinical trials are also discussed.
引用
收藏
页码:1011 / 1026
页数:16
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