Organoid culture systems for prostate epithelial and cancer tissue

Publication date

2016-02-01

Authors

Drost, Jarno
Karthaus, Wouter R
Gao, Dong
Driehuis, Else
Sawyers, Charles L.
Chen, Yu
Clevers, HansISNI 0000000043961208

Editors

Advisors

Supervisors

Document Type

Article

Collections

Open Access logo

License

taverne

Abstract

This protocol describes a strategy for the generation of 3D prostate organoid cultures from healthy mouse and human prostate cells (either bulk or FACS-sorted single luminal and basal cells), metastatic prostate cancer lesions and circulating tumor cells. Organoids derived from healthy material contain the differentiated luminal and basal cell types, whereas organoids derived from prostate cancer tissue mimic the histology of the tumor. We explain how to establish these cultures in the fully defined serum-free conditioned medium that is required to sustain organoid growth. Starting with the plating of digested tissue material, full-grown organoids can usually be obtained in ∼2 weeks. The culture protocol we describe here is currently the only one that allows the growth of both the luminal and basal prostatic epithelial lineages, as well as the growth of advanced prostate cancers. Organoids established using this protocol can be used to study many different aspects of prostate biology, including homeostasis, tumorigenesis and drug discovery.

Keywords

Taverne, General Biochemistry,Genetics and Molecular Biology, Journal Article, Research Support, Non-U.S. Gov't

Citation

Drost, J, Karthaus, W R, Gao, D, Driehuis, E, Sawyers, C L, Chen, Y & Clevers, H 2016, 'Organoid culture systems for prostate epithelial and cancer tissue', Nature Protocols, vol. 11, no. 2, pp. 347-358. https://doi.org/10.1038/nprot.2016.006