Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland, United States of America.
Department of Mechanical Engineering, Johns Hopkins University, Baltimore, Maryland, United States of America.
PLoS One. 2022 Mar 8;17(3):e0264907. doi: 10.1371/journal.pone.0264907. eCollection 2022.
Direct assessment of patient samples holds unprecedented potential in the treatment of cancer. Circulating tumor cells (CTCs) in liquid biopsies are a rapidly evolving source of primary cells in the clinic and are ideal candidates for functional assays to uncover real-time tumor information in real-time. However, a lack of routines allowing direct and active interrogation of CTCs directly from liquid biopsy samples represents a bottleneck for the translational use of liquid biopsies in clinical settings. To address this, we present a workflow for using a microfluidic vortex-assisted electroporation system designed for the functional assessment of CTCs purified from blood. Validation of this approach was assessed through drug response assays on wild-type (HCC827 wt) and gefitinib-resistant (HCC827 GR6) non-small cell lung cancer (NSCLC) cells. HCC827 cells trapped within microscale vortices were electroporated to sequentially deliver drug agents into the cytosol. Electroporation conditions facilitating multi-agent delivery were characterized for both cell lines using an automatic single-cell image fluorescence intensity algorithm. HCC827 GR6 cells spiked into the blood to emulate drug-resistant CTCs were able to be collected with high purity, demonstrating the ability of the device to minimize background cell impact for downstream sensitive cell assays. Using our proposed workflow, drug agent combinations to restore gefitinib sensitivity reflected the anticipated cytotoxic response. Taken together, these results represent a microfluidics multi-drug screening panel workflow that can enable functional interrogation of patient CTCs in situ, thereby accelerating the clinical standardization of liquid biopsies.
直接评估患者样本在癌症治疗中具有前所未有的潜力。液体活检中的循环肿瘤细胞 (CTC) 是临床中不断发展的原代细胞来源,非常适合用于功能测定,以实时揭示实时肿瘤信息。然而,缺乏允许直接和主动从液体活检样本中检测 CTC 的常规方法,是液体活检在临床环境中转化应用的一个瓶颈。为了解决这个问题,我们提出了一种使用微流控涡旋辅助电穿孔系统的工作流程,该系统专为从血液中纯化的 CTC 的功能评估而设计。通过对野生型 (HCC827 wt) 和吉非替尼耐药 (HCC827 GR6) 非小细胞肺癌 (NSCLC) 细胞的药物反应测定来验证这种方法。使用自动单细胞图像荧光强度算法对两种细胞系进行了电穿孔条件的表征,以促进多药物传递。使用我们提出的工作流程,能够恢复吉非替尼敏感性的药物组合反映了预期的细胞毒性反应。总之,这些结果代表了一种微流控多药物筛选面板工作流程,可实现对患者 CTC 的原位功能检测,从而加速液体活检的临床标准化。