Department of Pharmacology, Penn State College of Medicine, Penn State Milton S. Hershey Medical Center, Hershey, PA, USA.
Mol Diagn Ther. 2014 Apr;18(2):175-83. doi: 10.1007/s40291-013-0071-2.
Circulating melanoma cells (CMCs) are thought to be the foundation for metastatic disease, which makes this cancer especially lethal. Cancer cells contained in the primary tumor undergo genotypic and phenotypic changes leading to an epithelial-to-mesenchymal transition, during which numerous changes occur in signaling pathways and proteins in the cells. CMCs are then shed off or migrate from the primary tumor and intravasate the vasculature system. A few CMCs are able to survive in the circulation through expression of a variety of genes and also by evading immune system recognition to establish metastases at distant sites after extravasating from the vessels. The presence of CMCs in the blood of a melanoma patient can be used for disease staging, predicting metastasis development, and evaluating the efficacy of therapeutic agents. Overall survival and disease-free duration can also be correlated with the presence of CMCs. Finally, analysis of CMCs for druggable therapeutic gene targets could lead to the development of personalized treatment regimens to prevent metastasis. Thus, the study of CMCs shows promise for the detection, staging, and monitoring of disease treatment, as well as for determination of prognosis and predicting overall disease-free survival. These are the areas reviewed in this article.
循环黑素瘤细胞(CMCs)被认为是转移性疾病的基础,这使得这种癌症特别致命。原发性肿瘤中的癌细胞经历基因和表型的变化,导致上皮-间充质转化,在此过程中细胞中的信号通路和蛋白质发生许多变化。然后,CMC 从原发性肿瘤中脱落或迁移,并浸润脉管系统。少数 CMC 通过表达多种基因并逃避免疫系统识别,从而在从血管外渗后在远处部位建立转移,从而能够在循环中存活。黑素瘤患者血液中 CMC 的存在可用于疾病分期、预测转移发展以及评估治疗剂的疗效。总体生存和无病持续时间也与 CMC 的存在相关。最后,对 CMC 进行可用药治疗基因靶标的分析可能会导致开发个性化治疗方案以预防转移。因此,对 CMC 的研究有望用于检测、分期和监测疾病治疗,以及确定预后和预测总体无病生存。这是本文综述的领域。