College of Pharmacy and Biological Engineering, Chongqing University of Technology, Chongqing 400054, PR China.
Key Laboratory of Luminescence Analysis and Molecular Sensing, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.
Anal Chem. 2024 Feb 27;96(8):3329-3334. doi: 10.1021/acs.analchem.3c04135. Epub 2024 Feb 17.
Simultaneous detection of the concentration variations of microRNA-221 (miRNA-221) and PTEN mRNA molecules in the PI3K/AKT signaling pathway is of significance to elucidate cancer cell migration and invasion, which is useful for cancer diagnosis and therapy. In this work, we show the biodegradable MnO nanosheet-assisted and target-triggered DNAzyme recycling signal amplification cascaded approach for the specific detection of the PI3K/AKT signaling pathway in live cells via simultaneous and sensitive monitoring of the variation of intracellular miRNA-221 and PTEN mRNA. Our nanoprobes enable highly sensitive and multiplexed sensing of miRNA-221 and PTEN mRNA with low detection limits of 23.6 and 0.59 pM in vitro, respectively, due to the signal amplification cascades. Importantly, the nanoprobes can be readily delivered into cancer cells and the MnO nanosheets can be degraded by intracellular glutathione to release the Mn cofactors to trigger multiple DNAzyme recycling cycles to show highly enhanced fluorescence at different wavelengths to realize sensitive and multiplexed imaging of PTEN mRNA and miRNA-221 for detecting the PI3K/AKT signaling pathway. Moreover, the regulation of PTEN mRNA expression by miRNA-221 upon stimulation by various drugs can also be verified by our method, indicating its promising potentials for both disease diagnosis and drug screening.
同时检测 PI3K/AKT 信号通路中 microRNA-221(miRNA-221)和 PTEN mRNA 分子的浓度变化,对于阐明癌细胞的迁移和侵袭具有重要意义,有助于癌症的诊断和治疗。在这项工作中,我们展示了一种可生物降解的 MnO 纳米片辅助和靶触发的 DNA 酶循环信号放大级联方法,通过同时和敏感地监测细胞内 miRNA-221 和 PTEN mRNA 的变化,用于在活细胞中特异性检测 PI3K/AKT 信号通路。我们的纳米探针由于信号放大级联,可以实现对 miRNA-221 和 PTEN mRNA 的高灵敏度和多重检测,其体外检测限分别低至 23.6 和 0.59 pM。重要的是,纳米探针可以很容易地递送到癌细胞中,细胞内谷胱甘肽可以降解 MnO 纳米片,释放 Mn 辅因子,触发多个 DNA 酶循环,在不同波长下显示出高度增强的荧光,从而实现对 PTEN mRNA 和 miRNA-221 的灵敏和多重成像,以检测 PI3K/AKT 信号通路。此外,我们的方法还可以验证各种药物刺激下 miRNA-221 对 PTEN mRNA 表达的调节,表明其在疾病诊断和药物筛选方面具有广阔的应用前景。