Fu Xinping, Tao Lihua, Zhang Xiaoliu
Department of Biology and Biochemistry and Center for Nuclear Receptor and Cell Signaling, University of Houston, Houston, TX 77204, USA.
Mol Ther Methods Clin Dev. 2021 Aug 28;23:78-86. doi: 10.1016/j.omtm.2021.08.007. eCollection 2021 Dec 10.
The current methods for detecting circulating tumor cells (CTCs) suffer from several drawbacks. We report a novel method that is based on a chimeric virus probe and can detect CTCs with extremely high specificity and sensitivity. Moreover, it exclusively detects live CTCs, and its detection efficacy is not impacted by the variation of epithelial cell adhesion molecule (EpCAM) expression. The chimeric virus probe is composed of a capsid from human papillomavirus that provides the detection with high specificity and an SV40-based genome that can amplify extensively inside CTCs and, hence, endows the detection with high sensitivity. Furthermore, different marker genes can be incorporated into the probe to provide detection with versatility. These unique capabilities will likely improve the validity and utility of this CTC detection in several clinical applications, which is one of the drawbacks suffered by many of the current CTC detection methods.
目前检测循环肿瘤细胞(CTC)的方法存在若干缺陷。我们报告了一种基于嵌合病毒探针的新方法,该方法能够以极高的特异性和灵敏度检测CTC。此外,它仅检测活的CTC,其检测效果不受上皮细胞粘附分子(EpCAM)表达变化的影响。嵌合病毒探针由人乳头瘤病毒的衣壳组成,可提供高特异性检测,以及基于SV40的基因组,该基因组可在CTC内大量扩增,从而赋予检测高灵敏度。此外,不同的标记基因可整合到探针中以提供多功能检测。这些独特的能力可能会提高这种CTC检测在多种临床应用中的有效性和实用性,而这正是许多当前CTC检测方法所存在的缺陷之一。