Proteomics in melanoma biomarker discovery: great potential, many obstacles.

International journal of proteomics Pub Date : 2011-01-01 Epub Date: 2011-10-11 DOI:10.1155/2011/181890
Michael S Sabel, Yashu Liu, David M Lubman
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引用次数: 38

Abstract

The present clinical staging of melanoma stratifies patients into heterogeneous groups, resulting in the application of aggressive therapies to large populations, diluting impact and increasing toxicity. To move to a new era of therapeutic decisions based on highly specific tumor profiling, the discovery and validation of new prognostic and predictive biomarkers in melanoma is critical. Genomic profiling, which is showing promise in other solid tumors, requires fresh tissue from a large number of primary tumors, and thus faces a unique challenge in melanoma. For this and other reasons, proteomics appears to be an ideal choice for the discovery of new melanoma biomarkers. Several approaches to proteomics have been utilized in the search for clinically relevant biomarkers, but to date the results have been relatively limited. This article will review the present work using both tissue and serum proteomics in the search for melanoma biomarkers, highlighting both the relative advantages and disadvantages of each approach. In addition, we review several of the major obstacles that need to be overcome in order to advance the field.

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蛋白质组学在黑色素瘤生物标志物发现中的应用:潜力巨大,障碍重重。
目前黑色素瘤的临床分期将患者分成不同的群体,导致在大量人群中应用积极的治疗,稀释了影响并增加了毒性。为了进入基于高度特异性肿瘤分析的治疗决策的新时代,发现和验证新的黑色素瘤预后和预测性生物标志物至关重要。基因组图谱在其他实体肿瘤中显示出前景,但需要大量原发肿瘤的新鲜组织,因此在黑色素瘤中面临着独特的挑战。由于这个和其他原因,蛋白质组学似乎是发现新的黑色素瘤生物标志物的理想选择。蛋白质组学的几种方法已被用于寻找临床相关的生物标志物,但迄今为止,结果相对有限。本文将回顾目前使用组织和血清蛋白质组学寻找黑色素瘤生物标志物的工作,强调每种方法的相对优点和缺点。此外,我们回顾了为了推进该领域而需要克服的几个主要障碍。
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