Patient-Derived Microphysiological Systems for Precision Medicine

Authors
Ko, JihoonSong, JiyoungChoi, NakwonKim, Hong Nam
Issue Date
2024-03
Publisher
Wiley-Blackwell
Citation
Advanced Healthcare Materials, v.13, no.7
Abstract
Patient-derived microphysiological systems (P-MPS) have emerged as powerful tools in precision medicine that provide valuable insight into individual patient characteristics. This review discusses the development of P-MPS as an integration of patient-derived samples, including patient-derived cells, organoids, and induced pluripotent stem cells, into well-defined MPSs. Emphasizing the necessity of P-MPS development, its significance as a nonclinical assessment approach that bridges the gap between traditional in vitro models and clinical outcomes is highlighted. Additionally, guidance is provided for engineering approaches to develop microfluidic devices and high-content analysis for P-MPSs, enabling high biological relevance and high-throughput experimentation. The practical implications of the P-MPS are further examined by exploring the clinically relevant outcomes obtained from various types of patient-derived samples. The construction and analysis of these diverse samples within the P-MPS have resulted in physiologically relevant data, paving the way for the development of personalized treatment strategies. This study describes the significance of the P-MPS in precision medicine, as well as its unique capacity to offer valuable insights into individual patient characteristics. Microphysiological systems now integrate patient-derived samples, functioning as physiologically relevant avatars for high-throughput assays. This evolution addresses an unmet clinical need for a patient-centered nonclinical assessment platform, steering toward more precise and personalized approaches in medical research and drug development.image
Keywords
ON-A-CHIP; PLURIPOTENT STEM-CELLS; CIRCULATING TUMOR-CELLS; LUNG-CANCER ORGANOIDS; MICROFLUIDIC DEVICES; BREAST-CANCER; AUTOIMMUNE-DISEASES; PANCREATIC-CANCER; ENDOTHELIAL-CELLS; THERAPY RESPONSE; microphysiological system; patient-derived; physiologically-relevant; precision medicine
ISSN
2192-2640
URI
https://pubs.kist.re.kr/handle/201004/113082
DOI
10.1002/adhm.202303161
Appears in Collections:
KIST Article > 2023
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