Lin Millicent, Chen Jie-Fu, Lu Yi-Tsung, Zhang Yang, Song Jinzhao, Hou Shuang, Ke Zunfu, Tseng Hsian-Rong
Department of Pathology, The First Affiliated hospital of Sun Yat-sen University , Guangzhou, 510080 Guangdong, People's Republic of China.
Acc Chem Res. 2014 Oct 21;47(10):2941-50. doi: 10.1021/ar5001617. Epub 2014 Aug 11.
Circulating tumor cells (CTCs) are cancer cells that break away from either a primary tumor or a metastatic site and circulate in the peripheral blood as the cellular origin of metastasis. With their role as a "tumor liquid biopsy", CTCs provide convenient access to all disease sites, including that of the primary tumor and the site of fatal metastases. It is conceivable that detecting and analyzing CTCs will provide insightful information in assessing the disease status without the flaws and limitations encountered in performing conventional tumor biopsies. However, identifying CTCs in patient blood samples is technically challenging due to the extremely low abundance of CTCs among a large number of hematologic cells. To address this unmet need, there have been significant research endeavors, especially in the fields of chemistry, materials science, and bioengineering, devoted to developing CTC detection, isolation, and characterization technologies. Inspired by the nanoscale interactions observed in the tissue microenvironment, 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 high efficiency. The working mechanism of NanoVelcro cell-affinity substrates mimics that of Velcro: when the two fabric strips of a Velcro fastener are pressed together, tangling between the hairy surfaces on two strips leads to strong binding. Through continuous evolution, three generations (gens) of NanoVelcro CTC chips have been established to achieve different clinical utilities. The first-gen NanoVelcro chip, composed of a silicon nanowire substrate (SiNS) and an overlaid microfluidic chaotic mixer, was created for CTC enumeration. Side-by-side analytical validation studies using clinical blood samples suggested that the sensitivity of first-gen NanoVelcro chip outperforms that of FDA-approved CellSearch. In conjunction with the use of the laser microdissection (LMD) technique, second-gen NanoVelcro chips (i.e., NanoVelcro-LMD), based on polymer nanosubstrates, were developed for single-CTC isolation. The individually isolated CTCs can be subjected to single-CTC genotyping (e.g., Sanger sequencing and next-generation sequencing, NGS) to verify the CTC's role as tumor liquid biopsy. Created by grafting of thermoresponsive polymer brushes onto SiNS, third-gen NanoVelcro chips (i.e., Thermoresponsive NanoVelcro) have demonstrated the capture and release of CTCs at 37 and 4 °C, respectively. The temperature-dependent conformational changes of polymer brushes can effectively alter the accessibility of the capture agent on SiNS, allowing for rapid CTC purification with desired viability and molecular integrity. This Account summarizes the continuous evolution of NanoVelcro CTC assays from the emergence of the original idea all the way to their applications in cancer research. We envision that NanoVelcro CTC assays will lead the way for powerful and cost-efficient diagnostic platforms for researchers to better understand underlying disease mechanisms and for physicians to monitor real-time disease progression.
循环肿瘤细胞(CTCs)是从原发性肿瘤或转移部位脱离并在外周血中循环的癌细胞,是转移的细胞起源。作为一种“肿瘤液体活检”手段,CTCs为获取包括原发性肿瘤和致命转移部位在内的所有疾病部位的信息提供了便利途径。可以想象,检测和分析CTCs将为评估疾病状态提供有价值的信息,而不会出现传统肿瘤活检中遇到的缺陷和局限性。然而,由于患者血液样本中CTCs的丰度极低,在大量血液细胞中识别CTCs在技术上具有挑战性。为满足这一未被满足的需求,人们进行了大量研究工作,尤其是在化学、材料科学和生物工程领域,致力于开发CTCs检测、分离和表征技术。受组织微环境中观察到的纳米级相互作用的启发,加州大学洛杉矶分校的研究团队率先提出了“纳米魔术贴”细胞亲和底物的独特概念,其中涂有CTCs捕获剂的纳米结构底物被用于高效固定CTCs。纳米魔术贴细胞亲和底物的工作机制模仿了魔术贴:当魔术贴紧固件的两条织物条被压在一起时,两条条上毛状表面之间的缠结会导致牢固结合。通过不断发展,已建立了三代纳米魔术贴CTCs芯片以实现不同的临床应用。第一代纳米魔术贴芯片由硅纳米线底物(SiNS)和覆盖的微流体混沌混合器组成,用于CTCs计数。使用临床血液样本进行的并行分析验证研究表明,第一代纳米魔术贴芯片的灵敏度优于FDA批准的CellSearch。结合激光显微切割(LMD)技术,基于聚合物纳米底物开发了第二代纳米魔术贴芯片(即纳米魔术贴-LMD),用于单个CTCs的分离。单独分离的CTCs可进行单个CTCs基因分型(例如桑格测序和下一代测序,NGS),以验证CTCs作为肿瘤液体活检的作用。通过将热响应性聚合物刷嫁接到SiNS上创建的第三代纳米魔术贴芯片(即热响应性纳米魔术贴)已分别证明在37℃和4℃下对CTCs的捕获和释放。聚合物刷的温度依赖性构象变化可以有效地改变SiNS上捕获剂的可及性,从而以所需的活力和分子完整性快速纯化CTCs。本综述总结了纳米魔术贴CTCs检测方法从最初的想法出现到其在癌症研究中的应用的不断发展。我们设想,纳米魔术贴CTCs检测方法将为强大且经济高效的诊断平台引领道路,使研究人员能够更好地理解潜在的疾病机制,使医生能够实时监测疾病进展。