Clinical utility of non-EpCAM based circulating tumor cell assays

被引:31
作者
Austin, R. Garland [1 ]
Huang, Tony Jun [2 ,3 ]
Wu, Mengxi [4 ,5 ]
Armstrong, Andrew J. [1 ]
Zhang, Tian [1 ]
机构
[1] Duke Univ, Med Ctr, Duke Canc Inst, Div Med Oncol,Dept Med, Durham, NC 27706 USA
[2] Duke Univ, Dept Med Engn & Mat Sci, Durham, NC 27706 USA
[3] Duke Univ, Dept Biomed Engn, Durham, NC 27706 USA
[4] Penn State Univ, Dept Engn Sci & Mech, 227 Hammond Bldg, University Pk, PA 16802 USA
[5] Duke Univ, Dept Mech Engn & Mat Sci, Durham, NC 27706 USA
关键词
Nanotechnology; Circulating tumor cell; Biomarker; Liquid biopsy; METASTATIC BREAST-CANCER; EPITHELIAL-MESENCHYMAL TRANSITION; IRON-OXIDE NANOPARTICLES; PERIPHERAL-BLOOD; ULTRASENSITIVE DETECTION; MULTIVALENT BINDING; ENRICHMENT PROCESS; ADHESION MOLECULE; EFFICIENT CAPTURE; ENHANCED CAPTURE;
D O I
10.1016/j.addr.2018.01.013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Methods enabling the isolation, detection, and characterization of circulating tumor cells (CTCs) in blood have clear potential to facilitate precision medicine approaches in patients with cancer, not only for prognostic purposes but also for prediction of the benefits of specific therapies in oncology. However, current CTC assays, which capture CTCs based on expression of epithelial cell adhesion molecule (EpCAM), fail to capture cells from de-differentiated tumors and carcinomas undergoing loss of the epithelial phenotype during the invasion/metastatic process. To address this limitation, many groups are developing non-EpCAM based CTC assays that incorporate nanotechnology to improve test sensitivity for rare but important cells that may otherwise go undetected, and therefore may improve upon clinical utility. In this review, we outline emerging non-EpCAM based CTC assays utilizing nanotechnology approaches for CTC capture or characterization, including dendrimers, magnetic nanoparticles, gold nanoparticles, negative selection chip or software-based on-slide methods, and nano-scale substrates. In addition, we address challenges that remain for the clinical translation of these platforms. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:132 / 142
页数:11
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