State Key Laboratory of Bioelectronics (Chien-Shiung Wu Lab), School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, China.
Analyst. 2020 Feb 17;145(4):1294-1301. doi: 10.1039/c9an02390a.
Compared with normal cells, cancer or tumor cells have a specific microenvironment and apparently possess a relatively large amount of ROS/RNS, and their overexpression is one of the important reasons for tumor development and deterioration. Therefore, monitoring the changes of intracellular ROS/RNS can improve the awareness of the clinical manifestations of the disease, which will be beneficial for the early diagnosis of cancer and improving treatment efficiency. Herein, in this study we have exploited and constructed a novel strategy based on the SiC@C nanowire electrode for intracellular electrochemical analysis to monitor ROS levels in cancer or tumor cells. Firstly, the SiC@C nanowire electrode was utilized to detect the intracellular ROS radical changes involved in the relevant biological processes of cancer cells where fluorescent zinc nanoclusters were biosynthesized in situ in target cancer cells by using the intracellular microenvironment and specificity of these cancer cells. By combining a confocal fluorescence microscopy study simultaneously, our observations illustrate that accompanied by the apparent change of the intracellular ROS, these in situ biosynthesized fluorescent nanoclusters gradually accumulate inside the cytosolic area with the increase of the reaction time. Moreover, it is evident that the size of the SiC@C nanoelectrodes can match the single cell dimensions, and its unique high spatial resolution provides the possibility of relevant intracellular molecular detection. These nanoelectrochemical biosensors can be adopted to quantitatively determine the change of the ROS content in target single cells in the relevant biological microenvironment or during the in situ biosynthesis process, and are also beneficial for understanding the related mechanism of some specific biological processes including the in situ synthesis at the single cell level.
与正常细胞相比,癌细胞或肿瘤细胞具有特定的微环境,显然具有相对大量的 ROS/RNS,其过表达是肿瘤发展和恶化的重要原因之一。因此,监测细胞内 ROS/RNS 的变化可以提高对疾病临床表现的认识,这将有利于癌症的早期诊断和提高治疗效率。在本研究中,我们开发并构建了一种基于 SiC@C 纳米线电极的新型策略,用于细胞内电化学分析,以监测癌细胞或肿瘤细胞中的 ROS 水平。首先,利用 SiC@C 纳米线电极检测涉及癌细胞相关生物过程的细胞内 ROS 自由基变化,通过利用细胞内微环境和这些癌细胞的特异性,在靶癌细胞中原位生物合成荧光锌纳米簇。通过同时结合共聚焦荧光显微镜研究,我们的观察结果表明,伴随着细胞内 ROS 的明显变化,这些原位生物合成的荧光纳米簇随着反应时间的增加逐渐在细胞质区域内积累。此外,很明显 SiC@C 纳米电极的尺寸可以与单个细胞的尺寸相匹配,其独特的高空间分辨率为相关细胞内分子检测提供了可能性。这些纳米电化学生物传感器可用于定量测定相关生物微环境或原位生物合成过程中靶标单细胞中 ROS 含量的变化,也有利于理解包括单细胞水平原位合成在内的某些特定生物过程的相关机制。