Microfluidic Platform for Generating and Releasing Patient‐Derived Cancer Organoids with Diverse Shapes: Insight into Shape‐Dependent Tumor Growth

Author:

Kheiri Sina1ORCID,Yakavets Ilya2ORCID,Cruickshank Jennifer3,Ahmadi Fatemeh2,Berman Hal K34,Cescon David W.35,Young Edmond W.K.16,Kumacheva Eugenia267ORCID

Affiliation:

1. Department of Mechanical & Industrial Engineering University of Toronto 5 King's College Road Toronto ON M5S 3G8 Canada

2. Department of Chemistry University of Toronto 80 St. George Street Toronto ON M5S 3H6 Canada

3. Princess Margaret Cancer Centre University Health Network 610 University Avenue Toronto ON M5G 2C1 Canada

4. Department of Laboratory Medicine and Pathobiology University of Toronto 1 King's College Circle Toronto ON M5S 1A8 Canada

5. Department of Medicine University of Toronto 1 King's College Circle Toronto ON M5S 1A8 Canada

6. Institute of Biomedical Engineering University of Toronto 164 College Street Toronto ON M5S 3G9 Canada

7. Department of Chemical Engineering and Applied Chemistry University of Toronto 200 College Street Toronto ON M5S 3E5 Canada

Abstract

AbstractMulticellular spheroids and patient‐derived organoids find many applications in fundamental research, drug discovery, and regenerative medicine. Advances in the understanding and recapitulation of organ functionality and disease development require the generation of complex organoid models, including organoids with diverse morphologies. Microfluidics‐based cell culture platforms enable time‐efficient confined organoid generation. However, the ability to form organoids with different shapes with a subsequent transfer from microfluidic devices to unconstrained environments for studies of morphology‐dependent organoid growth is yet to be demonstrated. Here, a microfluidic platform is introduced that enables high‐fidelity formation and addressable release of breast cancer organoids with diverse shapes. Using this platform, the impact of organoid morphology on their growth in unconstrained biomimetic hydrogel is explored. It is shown that proliferative cancer cells tend to localize in high positive curvature organoid regions, causing their faster growth, while the overall growth pattern of organoids with diverse shapes tends to reduce interfacial tension at the organoid‐hydrogel interface. In addition to the formation of organoids with diverse morphologies, this platform can be integrated into multi‐tissue micro‐physiological systems.

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

Wiley

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