Szerenyi Dora, Jarvas Gabor, Guttman Andras
Research Institute of Biomolecular and Chemical Engineering, Faculty of Engineering, University of Pannonia, 8200 Veszprem, Hungary.
CAPTEC Medical Ltd., 8200 Veszprem, Hungary.
Molecules. 2025 Feb 20;30(5):976. doi: 10.3390/molecules30050976.
Circulating tumor cells (CTCs) are pivotal in cancer metastasis and serve as valuable biomarkers for diagnosis, prognosis, and treatment monitoring. Traditional CTC capture methods predominantly utilize the epithelial cell adhesion molecule (EpCAM) as a marker for isolation. However, the heterogeneity of these circulating cells and the epithelial-to-mesenchymal transition process (wherein epithelial cells acquire mesenchymal characteristics) limit the efficacy of EpCAM-based capture techniques. In this paper, we critically review the role of the EpCAM in CTC capture, explore the impact of epithelial-to-mesenchymal transition on EpCAM expression, and discuss alternative biomarkers and strategies to enhance CTC isolation. By evaluating the limitations of EpCAM-mediated capture and the challenges posed by epithelial-to-mesenchymal transition, we aim to provide insights into the development of more comprehensive liquid biopsy approaches for cancer management.
循环肿瘤细胞(CTCs)在癌症转移中起关键作用,并且作为用于诊断、预后和治疗监测的有价值的生物标志物。传统的CTCs捕获方法主要利用上皮细胞粘附分子(EpCAM)作为分离标志物。然而,这些循环细胞的异质性以及上皮-间质转化过程(其中上皮细胞获得间质特征)限制了基于EpCAM的捕获技术的功效。在本文中,我们批判性地综述了EpCAM在CTCs捕获中的作用,探讨了上皮-间质转化对EpCAM表达的影响,并讨论了替代生物标志物和增强CTCs分离的策略。通过评估EpCAM介导的捕获的局限性以及上皮-间质转化带来的挑战,我们旨在为开发更全面的用于癌症管理的液体活检方法提供见解。