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Zebrafish Patient-Derived Xenograft Model as a Preclinical Platform for Uveal Melanoma Drug Discovery

ORCID
0009-0005-6327-4273
Affiliation
Institute of Biology, Leiden University, 2333 BE Leiden, The Netherlands;(J.Y.);
Yin, Jie;
Affiliation
Institute of Biology, Leiden University, 2333 BE Leiden, The Netherlands;(J.Y.);
Zhao, Gangyin;
Affiliation
Liverpool Ocular Oncology Research Centre, Department of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool L69 3BX, UK
Kalirai, Helen;
ORCID
0000-0002-1464-2069
Affiliation
Liverpool Ocular Oncology Research Centre, Department of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool L69 3BX, UK
Coupland, Sarah E.;
ORCID
0000-0002-0570-7967
Affiliation
Department of Cell and Chemical Biology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands
Jochemsen, Aart G.;
ORCID
0000-0001-5976-4759
Affiliation
Institute of Biology, Leiden University, 2333 BE Leiden, The Netherlands;(J.Y.);
Forn-Cuní, Gabriel;
ORCID
0000-0002-3537-3662
Affiliation
Department of Ophthalmology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands
Wierenga, Annemijn P. A.;
ORCID
0000-0003-2261-3820
Affiliation
Department of Ophthalmology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands
Jager, Martine J.;
Affiliation
Institute of Biology, Leiden University, 2333 BE Leiden, The Netherlands;(J.Y.);
Snaar-Jagalska, B. Ewa;
Affiliation
Institute of Biology, Leiden University, 2333 BE Leiden, The Netherlands;(J.Y.);
Groenewoud, Arwin

Uveal melanoma (UM) is a rare malignant cancer of the eye, with up to 50% of patients dying from metastasis, for which no effective treatment is available. Due to the rarity of the disease, there is a great need to harness the limited material available from primary tumors and metastases for advanced research and preclinical drug screening. We established a platform to isolate, preserve, and transiently recover viable tissues, followed by the generation of spheroid cultures derived from primary UM. All assessed tumor-derived samples formed spheroids in culture within 24 h and stained positive for melanocyte-specific markers, indicating the retention of their melanocytic origin. These short-lived spheroids were only maintained for the duration of the experiment (7 days) or re-established from frozen tumor tissue acquired from the same patient. Intravenous injection of fluorescently labeled UM cells derived from these spheroids into zebrafish yielded a reproducible metastatic phenotype and recapitulated molecular features of the disseminating UM. This approach allowed for the experimental replications required for reliable drug screening (at least 2 individual biological experiments, with n > 20). Drug treatments with navitoclax and everolimus validated the zebrafish patient-derived model as a versatile preclinical tool for screening anti-UM drugs and as a preclinical platform to predict personalized drug responses.

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