Qiu Chun, Li Peng, Bi Jianjun, Wu Qing, Lu Linna, Qian Guanxiang, Jia Renbing, Jia Rong
School of Life Science, Anhui University, Hefei, Anhui 230601, P.R. China; Department of Ophthalmology, Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai 200011, P.R. China.
Department of Ophthalmology, Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai 200011, P.R. China.
Oncol Lett. 2016 Apr;11(4):2379-2383. doi: 10.3892/ol.2016.4280. Epub 2016 Feb 25.
Uveal melanoma (UM) is the most frequently occurring primary intraocular malignancy in adults. Tyrosinase (TYR) is a copper-containing enzyme and a type I membrane protein that is involved in the generation of melanin, the main pigment in vertebrates. TYR-related protein 1 (TYRP1) is regarded to have a crucial role in the immunotherapy of melanoma. As biomarkers, the TYR-related proteins, TYRP1 and TYRP2, exhibit specific expression in melanocytes, while also contributing to melanin synthesis within melanosomes. In the present study, the differential expression of TYRP1 was investigated at the mRNA, protein and morphological levels in four human UM cell lines (SP6.5, OM431, OCM1 and OCM290) and the human retinal pigment epithelium (RPE) cell line, using polymerase chain reaction, western blotting, immunocytochemistry and immunofluorescence staining. It was found that SP6.5 cells expressed the highest level of TYRP1, in comparison to SP6.5 OCM1 and OM431 cells, which produced less TYRP1, and OCM290 cells, which produced almost no TYRP1. No TYRP1 protein expression was identified in the RPE cell line. These findings indicate the potential use of TYRP1 in the development of therapy for UM.
葡萄膜黑色素瘤(UM)是成人中最常见的原发性眼内恶性肿瘤。酪氨酸酶(TYR)是一种含铜酶和I型膜蛋白,参与黑色素(脊椎动物中的主要色素)的生成。酪氨酸酶相关蛋白1(TYRP1)被认为在黑色素瘤的免疫治疗中起关键作用。作为生物标志物,TYR相关蛋白TYRP1和TYRP2在黑素细胞中表现出特异性表达,同时也有助于黑素小体内的黑色素合成。在本研究中,使用聚合酶链反应、蛋白质印迹、免疫细胞化学和免疫荧光染色,在四种人UM细胞系(SP6.5、OM431、OCM1和OCM290)和人视网膜色素上皮(RPE)细胞系中,从mRNA、蛋白质和形态学水平研究了TYRP1的差异表达。结果发现,与产生较少TYRP1的SP6.5、OCM1和OM431细胞以及几乎不产生TYRP1的OCM290细胞相比,SP6.5细胞表达的TYRP1水平最高。在RPE细胞系中未鉴定到TYRP1蛋白表达。这些发现表明TYRP1在UM治疗开发中的潜在用途。