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

被引:10
作者
Yin, Jie [1 ]
Zhao, Gangyin [1 ]
Kalirai, Helen [2 ]
Coupland, Sarah E. [2 ]
Jochemsen, Aart G. [3 ]
Forn-Cuni, Gabriel [1 ]
Wierenga, Annemijn P. A. [4 ]
Jager, Martine J. [4 ]
Snaar-Jagalska, B. Ewa [1 ]
Groenewoud, Arwin [1 ,5 ]
机构
[1] Leiden Univ, Inst Biol, NL-2333 BE Leiden, Netherlands
[2] Univ Liverpool, Liverpool Ocular Oncol Res Ctr, Dept Mol & Clin Canc Med, Liverpool L69 3BX, England
[3] Leiden Univ, Dept Cell & Chem Biol, Med Ctr, NL-2333 ZA Leiden, Netherlands
[4] Leiden Univ, Dept Ophthalmol, Med Ctr, NL-2333 ZA Leiden, Netherlands
[5] Friedrich Alexander Univ Erlangen Nurnberg FAU, Inst Pathol, Dept Nephropathol, Expt Renal & Cardiovasc Res, D-91054 Erlangen, Germany
基金
欧盟地平线“2020”;
关键词
eye; oncology; uveal melanoma; xenograft; zebrafish; drug toxicity; drug screening; HUMAN CANCER; IN-VIVO; THERAPY; METASTASIS; ESTABLISHMENT;
D O I
10.3390/ph16040598
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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.
引用
收藏
页数:16
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