Hu Chen, Dief Essam M, Soliman Bram G, Romanazzo Sara, Rana Shilpa, Kilian Kristopher A, Tilley Richard D, Gooding J Justin
School of Chemistry, Australian Centre for NanoMedicine, University of New South Wales Sydney NSW 2052 Australia
School of Materials Science and Engineering, University of New South Wales Sydney NSW 2052 Australia.
Chem Sci. 2025 Apr 16. doi: 10.1039/d5sc01036e.
Exploring cancer heterogeneity is crucial for both understanding cancer and developing prognostic tools to monitor cancer progression during treatment through the liquid biopsy concept. Herein, a nanoparticle-based "dispersible electrodes" biosensor was used to detect ultra-low concentrations of microRNA-155 (miRNA-155) from a single breast cancer spheroid for the first time. The results from the sensor were comparable to the standard real-time polymerase chain reaction analysis, but in a much shorter detection time and without any sample purification or amplification. Owing to the unique ability of the sensor to measure biomarker expression from unaltered and undiluted cancer liquid biopsy from a single cancer spheroid, we then tracked dynamic changes in miRNA-155 expression in a single spheroid treated with the anti-cancer drug doxorubicin. The ability to track dynamic biomarker changes in a single cancer spheroid opens the door to understanding key biological processes such as response to treatment on the cellular and molecular levels, paving the way for adapting liquid biopsy insights to guide oncologists and more personalised treatment strategies.
探索癌症异质性对于理解癌症以及开发预后工具以通过液体活检概念监测治疗期间的癌症进展都至关重要。在此,一种基于纳米颗粒的“可分散电极”生物传感器首次用于从单个乳腺癌球体中检测超低浓度的微小RNA - 155(miRNA - 155)。该传感器的检测结果与标准实时聚合酶链反应分析相当,但检测时间更短,且无需任何样品纯化或扩增。由于该传感器具有从单个癌症球体未改变和未稀释的癌症液体活检中测量生物标志物表达的独特能力,我们随后追踪了用抗癌药物阿霉素处理的单个球体中miRNA - 155表达的动态变化。在单个癌症球体中追踪生物标志物动态变化的能力为理解关键生物学过程(如细胞和分子水平上对治疗的反应)打开了大门,为将液体活检见解应用于指导肿瘤学家和制定更个性化的治疗策略铺平了道路。