TY - JOUR
T1 - Cancer extracellular vesicles, tumoroid models, and tumor microenvironment
AU - Eguchi, Takanori
AU - Sheta, Mona
AU - Fujii, Masanori
AU - Calderwood, Stuart K.
N1 - Funding Information:
Takanori Eguchi was funded by JSPS Kakenhi Grants 17K11642-TE , 19H03817-MT , 20H03888-HN , 20K09904-CS , and 21K08902-HY . Stuart K. Calderwood was funded by NIH under Grant RO1CA176326 and CA176326-05 .
Publisher Copyright:
© 2022
PY - 2022
Y1 - 2022
N2 - Cancer extracellular vesicles (EVs), or exosomes, promote tumor progression through enhancing tumor growth, initiating epithelial-to-mesenchymal transition, remodeling the tumor microenvironment, and preparing metastatic niches. Three-dimensionally (3D) cultured tumoroids / spheroids aim to reproduce some aspects of tumor behavior in vitro and show increased cancer stem cell properties. These properties are transferred to their EVs that promote tumor growth. Moreover, recent tumoroid models can be furnished with aspects of the tumor microenvironment, such as vasculature, hypoxia, and extracellular matrix. This review summarizes tumor tissue culture and engineering platforms compatible with EV research. For example, the combination experiments of 3D-tumoroids and EVs have revealed multifunctional proteins loaded in EVs, such as metalloproteinases and heat shock proteins. EVs or exosomes are able to transfer their cargo molecules to recipient cells, whose fates are often largely altered. In addition, the review summarizes approaches to EV labeling technology using fluorescence and luciferase, useful for studies on EV-mediated intercellular communication, biodistribution, and metastatic niche formation.
AB - Cancer extracellular vesicles (EVs), or exosomes, promote tumor progression through enhancing tumor growth, initiating epithelial-to-mesenchymal transition, remodeling the tumor microenvironment, and preparing metastatic niches. Three-dimensionally (3D) cultured tumoroids / spheroids aim to reproduce some aspects of tumor behavior in vitro and show increased cancer stem cell properties. These properties are transferred to their EVs that promote tumor growth. Moreover, recent tumoroid models can be furnished with aspects of the tumor microenvironment, such as vasculature, hypoxia, and extracellular matrix. This review summarizes tumor tissue culture and engineering platforms compatible with EV research. For example, the combination experiments of 3D-tumoroids and EVs have revealed multifunctional proteins loaded in EVs, such as metalloproteinases and heat shock proteins. EVs or exosomes are able to transfer their cargo molecules to recipient cells, whose fates are often largely altered. In addition, the review summarizes approaches to EV labeling technology using fluorescence and luciferase, useful for studies on EV-mediated intercellular communication, biodistribution, and metastatic niche formation.
KW - 3D tumoroid models
KW - Cancer stem cells
KW - Exosome
KW - Extracellular vesicles
KW - Metastatic niche
KW - Tumor microenvironment
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U2 - 10.1016/j.semcancer.2022.01.003
DO - 10.1016/j.semcancer.2022.01.003
M3 - Article
C2 - 35032650
AN - SCOPUS:85122935643
SN - 1044-579X
JO - Seminars in Cancer Biology
JF - Seminars in Cancer Biology
ER -