Mouse models of uveal melanoma: Strengths, weaknesses, and future directions

被引:20
|
作者
Richards, Jackson R. [1 ,2 ]
Yoo, Jae Hyuk [2 ]
Shin, Donghan [2 ]
Odelberg, Shannon J. [2 ,3 ,4 ]
机构
[1] Univ Utah, Dept Oncol Sci, Salt Lake City, UT USA
[2] Univ Utah, Program Mol Med, Salt Lake City, UT USA
[3] Univ Utah, Dept Internal Med, Div Cardiovasc, Salt Lake City, UT 84112 USA
[4] Univ Utah, Dept Neurobiol & Anat, Salt Lake City, UT USA
基金
美国国家卫生研究院;
关键词
melanoma; mouse; transgenic mouse; uveal; xenograft; METASTATIC OCULAR MELANOMA; PATIENT-DERIVED ORGANOIDS; MURINE MODEL; CELL-LINES; IN-VITRO; INTRAOCULAR MELANOMAS; C-MET; SOMATIC MUTATIONS; TUMOR XENOGRAFTS; LIVER METASTASIS;
D O I
10.1111/pcmr.12853
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Uveal melanoma is the most common primary malignancy of the eye, and a number of discoveries in the last decade have led to a more thorough molecular characterization of this cancer. However, the prognosis remains dismal for patients with metastases, and there is an urgent need to identify treatments that are effective for this stage of disease. Animal models are important tools for preclinical studies of uveal melanoma. A variety of models exist, and they have specific advantages, disadvantages, and applications. In this review article, these differences are explored in detail, and ideas for new models that might overcome current challenges are proposed.
引用
收藏
页码:264 / 278
页数:15
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