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葡萄膜黑色素瘤转移模型

Uveal Melanoma Metastasis Models.

作者信息

Yang Hua, Cao Jinfeng, Grossniklaus Hans E

机构信息

Department of Ophthalmology, School of Medicine, Emory University, Atlanta, Ga., USA.

Department of Ophthalmology, LUMC, Leiden, The Netherlands.

出版信息

Ocul Oncol Pathol. 2015 Apr;1(3):151-60. doi: 10.1159/000370153. Epub 2015 Apr 9.

Abstract

Metastatic disease is the leading cause of death among patients with uveal melanoma. Treatment options for patients with clinically disseminated disease are usually unsuccessful. In vitro and in vivo models are important tools to investigate the pathogenesis of metastatic uveal melanomas and develop treatments for the metastases. In vitro experimental approaches focusing on cell invasion/migration which mimic the steps of the complex metastatic process may also be used for the identification of potential anti-invasion/migration drugs that may inhibit the spreading of tumor cells or the development of metastases. The effects of these drugs must subsequently be confirmed in reliable in vivo models before entering the clinical trial phase. Several models of intraocular melanoma with metastases in rodents and rabbits are currently being used. Most experimental models of uveal melanoma metastases require injection or implantation of melanoma cells into orthotopic locations, including into the liver, spleen, tail vein, or the left ventricle of the heart, in order to mimic the metastatic process.

摘要

转移性疾病是葡萄膜黑色素瘤患者的主要死因。临床播散性疾病患者的治疗选择通常并不成功。体外和体内模型是研究转移性葡萄膜黑色素瘤发病机制和开发转移灶治疗方法的重要工具。专注于模拟复杂转移过程步骤的细胞侵袭/迁移的体外实验方法,也可用于识别可能抑制肿瘤细胞扩散或转移灶发展的潜在抗侵袭/迁移药物。在进入临床试验阶段之前,这些药物的效果必须随后在可靠的体内模型中得到证实。目前正在使用几种啮齿动物和兔子发生转移的眼内黑色素瘤模型。大多数葡萄膜黑色素瘤转移的实验模型需要将黑色素瘤细胞注射或植入原位,包括肝脏、脾脏、尾静脉或心脏左心室,以模拟转移过程。

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