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Circulating melanoma cells in the diagnosis and monitoring of melanoma: an appraisal of clinical potential.

机译:循环中的黑色素瘤细胞在黑色素瘤的诊断和监测中:对临床潜力的评估。

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摘要

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.
机译:循环黑素瘤细胞(CMC)被认为是转移性疾病的基础,这使这种癌症特别致命。原发性肿瘤中包含的癌细胞发生基因型和表型改变,导致上皮到间充质转变,在此期间,细胞中的信号传导途径和蛋白质发生了许多变化。然后,CMC脱落或从原发肿瘤中迁移出来,并侵入脉管系统。一些CMC能够通过多种基因的表达在循环中幸存下来,并且还可以逃避免疫系统的识别,从血管中渗出后在远处建立转移灶。黑色素瘤患者血液中CMC的存在可用于疾病分期,预测转移的发展以及评估治疗剂的功效。总体生存率和无病持续时间也可能与CMC的存在相关。最后,对可药物治疗的基因靶标的CMC的分析可能会导致个性化治疗方案的发展,以防止转移。因此,CMCs的研究显示出有望用于疾病治疗的检测,分期和监测,以及确定预后和预测总体无病生存期。这些是本文中回顾的领域。

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