TY - JOUR
T1 - Tumor-on-chip modeling of organ-specific cancer and metastasis
AU - Del Piccolo, Nuala
AU - Shirure, Venktesh S.
AU - Bi, Ye
AU - Goedegebuure, S. Peter
AU - Gholami, Sepideh
AU - Hughes, Christopher C.W.
AU - Fields, Ryan C.
AU - George, Steven C.
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2021/8
Y1 - 2021/8
N2 - Every year, cancer claims millions of lives around the globe. Unfortunately, model systems that accurately mimic human oncology – a requirement for the development of more effective therapies for these patients – remain elusive. Tumor development is an organ-specific process that involves modification of existing tissue features, recruitment of other cell types, and eventual metastasis to distant organs. Recently, tissue engineered microfluidic devices have emerged as a powerful in vitro tool to model human physiology and pathology with organ-specificity. These organ-on-chip platforms consist of cells cultured in 3D hydrogels and offer precise control over geometry, biological components, and physiochemical properties. Here, we review progress towards organ-specific microfluidic models of the primary and metastatic tumor microenvironments. Despite the field's infancy, these tumor-on-chip models have enabled discoveries about cancer immunobiology and response to therapy. Future work should focus on the development of autologous or multi-organ systems and inclusion of the immune system.
AB - Every year, cancer claims millions of lives around the globe. Unfortunately, model systems that accurately mimic human oncology – a requirement for the development of more effective therapies for these patients – remain elusive. Tumor development is an organ-specific process that involves modification of existing tissue features, recruitment of other cell types, and eventual metastasis to distant organs. Recently, tissue engineered microfluidic devices have emerged as a powerful in vitro tool to model human physiology and pathology with organ-specificity. These organ-on-chip platforms consist of cells cultured in 3D hydrogels and offer precise control over geometry, biological components, and physiochemical properties. Here, we review progress towards organ-specific microfluidic models of the primary and metastatic tumor microenvironments. Despite the field's infancy, these tumor-on-chip models have enabled discoveries about cancer immunobiology and response to therapy. Future work should focus on the development of autologous or multi-organ systems and inclusion of the immune system.
KW - Metastatic niche
KW - Microfluidic model
KW - Microphysiological system
KW - Organ-on-chip
KW - Tissue engineering
KW - Tumor microenvironment
UR - http://www.scopus.com/inward/record.url?scp=85109189494&partnerID=8YFLogxK
U2 - 10.1016/j.addr.2021.05.008
DO - 10.1016/j.addr.2021.05.008
M3 - Review article
C2 - 34015419
AN - SCOPUS:85109189494
SN - 0169-409X
VL - 175
JO - Advanced Drug Delivery Reviews
JF - Advanced Drug Delivery Reviews
M1 - 113798
ER -