Stei Marta M, Loeffler Karin U, Holz Frank G, Herwig Martina C
Department of Ophthalmology, University of Bonn, Ernst-Abbe-Straße 2, 53127 Bonn, Germany.
Biomed Res Int. 2016;2016:4521807. doi: 10.1155/2016/4521807. Epub 2016 Jun 6.
Animal models serve as powerful tools for investigating the pathobiology of cancer, identifying relevant pathways, and developing novel therapeutic agents. They have facilitated rapid scientific progress in many tumor entities. However, for establishing a powerful animal model of uveal melanoma fundamental challenges remain. To date, no animal model offers specific genetic attributes as well as histologic, immunologic, and metastatic features of uveal melanoma. Syngeneic models with intraocular injection of cutaneous melanoma cells may suit best for investigating immunologic/tumor biology aspects. However, differences between cutaneous and uveal melanoma regarding genetics and metastasis remain problematic. Human xenograft models are widely used for evaluating novel therapeutics but require immunosuppression to allow tumor growth. New approaches aim to establish transgenic mouse models of spontaneous uveal melanoma which recently provided preliminary promising results. Each model provides certain benefits and may render them suitable for answering a respective scientific question. However, all existing models also exhibit relevant limitations which may have led to delayed research progress. Despite refined therapeutic options for the primary ocular tumor, patients' prognosis has not improved since the 1970s. Basic research needs to further focus on a refinement of a potent animal model which mimics uveal melanoma specific mechanisms of progression and metastasis. This review will summarise and interpret existing animal models of uveal melanoma including recent advances in the field.
动物模型是研究癌症病理生物学、确定相关通路以及开发新型治疗药物的有力工具。它们推动了许多肿瘤实体的科学进展。然而,要建立一个强大的葡萄膜黑色素瘤动物模型,仍面临根本性挑战。迄今为止,尚无动物模型具备葡萄膜黑色素瘤的特定基因特征以及组织学、免疫学和转移特征。眼内注射皮肤黑色素瘤细胞的同基因模型可能最适合研究免疫/肿瘤生物学方面。然而,皮肤黑色素瘤和葡萄膜黑色素瘤在遗传学和转移方面的差异仍然存在问题。人异种移植模型广泛用于评估新型疗法,但需要免疫抑制以促进肿瘤生长。新方法旨在建立自发葡萄膜黑色素瘤的转基因小鼠模型,最近已取得初步的有前景的结果。每种模型都有一定的优势,可能适合回答各自的科学问题。然而,所有现有模型也都存在相关局限性,这可能导致研究进展延迟。尽管针对原发性眼内肿瘤有了更精细的治疗选择,但自20世纪70年代以来,患者的预后并未改善。基础研究需要进一步聚焦于完善一种强大的动物模型,该模型能模拟葡萄膜黑色素瘤进展和转移的特定机制。本综述将总结和解读现有的葡萄膜黑色素瘤动物模型,包括该领域的最新进展。