Genetics of uveal melanoma

被引:0
|
作者
Wackernagel, W. [1 ]
Schneider, M. [1 ]
Mayer, C. [1 ]
Langmann, G. [1 ]
Singh, A. D. [2 ]
机构
[1] Med Univ Graz, Univ Augenklin Graz, Dept Ophthalmol, A-8036 Graz, Austria
[2] Cleveland Clin Fdn, Cole Eye Inst, Dept Ophthalm Oncol, Cleveland, OH 44195 USA
关键词
Uveal melanoma; clinical genetics; cytogenetics; molecular genetics; prognosis; IN-SITU HYBRIDIZATION; COMPARATIVE GENOMIC HYBRIDIZATION; INTRAOCULAR MALIGNANT-MELANOMA; DYSPLASTIC NEVUS SYNDROME; KINASE-4 INHIBITOR GENE; FAMILIAL ATYPICAL MOLE; DISEASE-FREE SURVIVAL; TUMOR-SUPPRESSOR; OCULAR MELANOMA; TGF-BETA;
D O I
10.1007/s00717-009-0360-7
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Uveal melanoma is a rare sporadic tumor with high mortality. Despite all advances in the treatment of this malignancy, mortality rate has not improved over the past decades. Tremendous advances in research on the development of uveal melanoma and metastatic disease have changed our understanding of this disease over the past years. New insights into the genetic and molecular fundamentals of uveal melanoma show first impacts in the clinical management of affected patients, and there is reason for hope, that the development of new treatments will improve the still poor prognosis. The objective of this work is to provide an overview on our current understanding of clinical genetics, cyto- and molecular genetics, to explain recent research in this field and to describe how recent findings have already begun to change the treatment of uveal melanoma patients.
引用
收藏
页码:319 / 332
页数:14
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