Urologic Oncology Program and Uro-Oncology Research Laboratories, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA; Department of Molecular and Medical Pharmacology, California NanoSystems Institute, Crump Institute for Molecular Imaging, University of California, Los Angeles, Los Angeles, CA, USA.
Urologic Oncology Program and Uro-Oncology Research Laboratories, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Adv Drug Deliv Rev. 2018 Feb 1;125:78-93. doi: 10.1016/j.addr.2018.03.006. Epub 2018 Mar 15.
Circulating tumor cells (CTCs) are cancer cells shredded from either a primary tumor or a metastatic site and circulate in the blood as the potential cellular origin of metastasis. By detecting and analyzing CTCs, we will be able to noninvasively monitor disease progression in individual cancer patients and obtain insightful information for assessing disease status, thus realizing the concept of "tumor liquid biopsy". However, it is technically challenging to identify CTCs in patient blood samples because of the extremely low abundance of CTCs among a large number of hematologic cells. In order to address this challenge, our research team at UCLA pioneered a unique concept of "NanoVelcro" cell-affinity substrates, in which CTC capture agent-coated nanostructured substrates were utilized to immobilize CTCs with remarkable efficiency. Four generations of NanoVelcro CTC assays have been developed over the past decade for a variety of clinical utilities. The 1st-gen NanoVelcro Chips, composed of a silicon nanowire substrate (SiNS) and an overlaid microfluidic chaotic mixer, were created for CTC enumeration. The 2nd-gen NanoVelcro Chips (i.e., NanoVelcro-LMD), based on polymer nanosubstrates, were developed for single-CTC isolation in conjunction with the use of the laser microdissection (LMD) technique. By grafting thermoresponsive polymer brushes onto SiNS, the 3rd-gen Thermoresponsive NanoVelcro Chips have demonstrated the capture and release of CTCs at 37 and 4 °C respectively, thereby allowing for rapid CTC purification while maintaining cell viability and molecular integrity. Fabricated with boronic acid-grafted conducting polymer-based nanomaterial on chip surface, the 4th-gen NanoVelcro Chips (Sweet chip) were able to purify CTCs with well-preserved RNA transcripts, which could be used for downstream analysis of several cancer specific RNA biomarkers. In this review article, we will summarize the development of the four generations of NanoVelcro CTC assays, and the clinical applications of each generation of devices.
循环肿瘤细胞(CTCs)是从原发性肿瘤或转移性肿瘤中破碎的癌细胞,在血液中循环,是转移的潜在细胞起源。通过检测和分析 CTCs,我们将能够无创地监测个体癌症患者的疾病进展,并获得评估疾病状态的有见地的信息,从而实现“肿瘤液体活检”的概念。然而,由于大量血液细胞中 CTCs 的含量极低,因此在患者血液样本中识别 CTCs 在技术上具有挑战性。为了应对这一挑战,我们加州大学洛杉矶分校的研究团队首创了一种独特的“纳米魔术贴”细胞亲和基质的概念,其中使用 CTC 捕获剂涂覆的纳米结构基质来高效地固定 CTCs。在过去十年中,为了各种临床应用,已经开发了四代 NanoVelcro CTC 检测。第一代 NanoVelcro 芯片,由硅纳米线基底(SiNS)和覆盖的微流混沌混合器组成,用于 CTC 计数。第二代 NanoVelcro 芯片(即 NanoVelcro-LMD),基于聚合物纳米基底,与激光微切割(LMD)技术结合使用,用于单个 CTC 的分离。通过将温敏聚合物刷接枝到 SiNS 上,第三代热敏 NanoVelcro 芯片分别在 37°C 和 4°C 时展示了 CTC 的捕获和释放,从而在保持细胞活力和分子完整性的同时,实现了快速的 CTC 纯化。第四代 NanoVelcro 芯片(甜蜜芯片)在芯片表面用接枝硼酸的导电聚合物基纳米材料制造,能够纯化 RNA 转录物保存完好的 CTCs,可用于下游分析几种癌症特异性 RNA 生物标志物。在这篇综述文章中,我们将总结四代 NanoVelcro CTC 检测的发展,以及每一代设备的临床应用。