Animal models of uveal melanoma

被引:8
作者
Uner, Ogul E. [1 ]
Gandrakota, Nikhila [2 ,3 ]
Azarcon, Corrina P. [1 ]
Grossniklaus, Hans E. [1 ,4 ,5 ]
机构
[1] Emory Univ, Dept Ophthalmol, Sch Med, Atlanta, GA USA
[2] Emory Univ, Sch Med, Dept Family Med, Atlanta, GA USA
[3] Emory Univ, Rollins Sch Publ Hlth, Atlanta, GA USA
[4] Emory Univ, Sch Med, Dept Pathol, Atlanta, GA USA
[5] Emory Univ, Dept Ophthalmol, 1365B Clifton Rd, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
Uveal melanoma (UM); ocular melanoma; animal model; xenograft; transgenic mice; PIGMENTED INTRAOCULAR TUMORS; METASTATIC OCULAR MELANOMA; HAMSTER GREENE MELANOMA; MOUSE MODEL; CHOROIDAL MELANOMA; MURINE MODEL; CELL-LINES; TRANSGENIC MICE; MALIGNANT-MELANOMA; RABBIT MODEL;
D O I
10.21037/aes-21-30
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Animal models are crucial for the study of tumorigenesis and therapies in oncology research. Though rare, uveal melanoma (UM) is the most common intraocular tumor and remains one of the most lethal cancers. Given the limitations of studying human UM cells in vitro, animal models have emerged as excellent platforms to investigate disease onset, progression, and metastasis. Since Greene's initial studies on hamster UM, researchers have dramatically improved the array of animal models. Animals with spontaneous tumors have largely been replaced by engrafted and genetically engineered models. Inoculation techniques continue to be refined and expanded. Newer methods for directed mutagenesis have formed transgenic models to reliably study primary tumorigenesis. Human UM cell lines have been used to generate rapidly growing xenografts. Most recently, patient-derived xenografts have emerged as models that closely mimic the behavior of human UM. Separate animal models to study metastatic UM have also been established. Despite the advancements, the prognosis has only recently improved for UM patients, especially in patients with metastases. There is a need to identify and evaluate new preclinical models. To accomplish this goal, it is important to understand the origin, methods, advantages, and disadvantages of current animal models. In this review, the authors present current and historic animal models for the experimental study of UM. The strengths and shortcomings of each model are discussed and potential future directions are explored.
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页数:20
相关论文
共 143 条
[1]  
ALBERT D M, 1980, International Ophthalmology Clinics, V20, P143, DOI 10.1097/00004397-198002020-00013
[2]  
ALBERT DM, 1981, INVEST OPHTH VIS SCI, V20, P606
[3]   The biology of uveal melanoma [J].
Amaro, Adriana ;
Gangemi, Rosaria ;
Piaggio, Francesca ;
Angelini, Giovanna ;
Barisione, Gaia ;
Ferrini, Silvano ;
Pfeffer, Ulrich .
CANCER AND METASTASIS REVIEWS, 2017, 36 (01) :109-140
[4]   Inhibition of NF-κB-Dependent Signaling Enhances Sensitivity and Overcomes Resistance to BET Inhibition in Uveal Melanoma [J].
Ambrosini, Grazia ;
Do, Catherine ;
Tycko, Benjamin ;
Realubit, Ronald B. ;
Karan, Charles ;
Musi, Elgilda ;
Carvajal, Richard D. ;
Chua, Vivian ;
Aplin, Andrew E. ;
Schwartz, Gary K. .
CANCER RESEARCH, 2019, 79 (09) :2415-2425
[5]  
ANAND R, 1994, INVEST OPHTH VIS SCI, V35, P3533
[6]   Uveal Melanoma: 5-Year Update on Incidence, Treatment, and Survival (SEER 1973-2013) [J].
Aronow, Mary E. ;
Topham, Allan K. ;
Singh, Arun D. .
OCULAR ONCOLOGY AND PATHOLOGY, 2018, 4 (03) :145-151
[7]  
Bérubé M, 2005, MOL VIS, V11, P1101
[8]  
Blanco G, 2000, CURR EYE RES, V21, P740, DOI 10.1076/0271-3683(200009)21:3
[9]  
1-R
[10]  
FT740