Taussig Cancer Center, Cleveland, OH, USA.
Future Oncol. 2012 Feb;8(2):205-15. doi: 10.2217/fon.11.150.
Uveal melanoma disseminates hematogenously, and blood biomarkers may be useful for prognosis and for monitoring disease progression. Melanoma-associated, metastatic and immune factors have been measured in the blood of patients with uveal melanoma, as have circulating melanoma cells. Most of the biomarkers were derived from studies in cutaneous melanoma. For various biological and/or technical reasons, these assessments have not demonstrated the accuracy required for effective prognostic or monitoring assays. Advances in uveal melanoma genomics and proteomics have generated many candidate biomarkers that are potentially measurable in blood. Measuring circulating nucleic acids may also be possible. Improvements in molecular profiling techniques that accurately predict metastatic risk in uveal melanoma patients should facilitate biomarker discovery and aid implementation in clinical testing. The stage is set to translate the advances made in understanding the molecular characteristics of uveal melanoma in order to identify and test clinically useful blood biomarkers of tumor dissemination and/or progression.
葡萄膜黑色素瘤通过血液播散,血液生物标志物可能对预后和监测疾病进展有用。已在葡萄膜黑色素瘤患者的血液中测量了黑色素瘤相关的、转移性的和免疫因素,以及循环黑素瘤细胞。大多数生物标志物来自皮肤黑色素瘤的研究。由于各种生物学和/或技术原因,这些评估并未显示出进行有效预后或监测检测所需的准确性。葡萄膜黑色素瘤基因组学和蛋白质组学的进步产生了许多潜在可在血液中测量的候选生物标志物。测量循环核酸也可能是可行的。改进能够准确预测葡萄膜黑色素瘤患者转移风险的分子谱分析技术,将有助于发现生物标志物并促进其在临床检测中的应用。目前的情况是,为了识别和测试肿瘤播散和/或进展的临床有用的血液生物标志物,需要将对葡萄膜黑色素瘤分子特征的理解方面的进展转化为实际应用。