Emamiamin Afsaneh, Shariati Pour Seyedeh Rojin, Serra Thea, Calabria Donato, Varone Marta, Di Nardo Fabio, Guardigli Massimo, Anfossi Laura, Baggiani Claudio, Zangheri Martina, Mirasoli Mara
Department of Chemistry "Giacomo Ciamician", Alma Mater Studiorum, University of Bologna, Tecnopolo di Rimini, Via Dario Campana 71, I-47922 Rimini, Italy.
Department of Chemistry, University of Turin, Via P. Giuria 5, I-10125 Turin, Italy.
Biosensors (Basel). 2025 Apr 8;15(4):238. doi: 10.3390/bios15040238.
MicroRNAs (miRNAs), which circulate in the serum and plasma, play a role in several biological processes, and their levels in body fluids are associated with the pathogenesis of various diseases, including different types of cancer. For this reason, miRNAs are considered promising candidates as biomarkers for diagnostic purposes, enabling the early detection of pathological onset and monitoring drug responses during therapy. However, current methods for miRNA quantification, such as northern blotting, isothermal amplification, RT-PCR, microarrays, and next-generation sequencing, are limited by their reliance on centralized laboratories, high costs, and the need for specialized personnel. Consequently, the development of sensitive, simple, and one-step analytical techniques for miRNA detection is highly desirable, particularly given the importance of early diagnosis and prompt treatment in cases of cancer. Lateral flow assays (LFAs) are among the most attractive point-of-care (POC) devices for healthcare applications. These systems allow for the rapid and straightforward detection of analytes using low-cost setups that are accessible to a wide audience. This review focuses on LFA-based methods for detecting and quantifying miRNAs associated with the diagnosis of various cancers, with particular emphasis on sensitivity enhancements achieved through the application of different labels and detection systems. Early, non-invasive detection of these diseases through the quantification of tailored biomarkers can significantly reduce mortality, improve survival rates, and lower treatment costs.
循环于血清和血浆中的微小RNA(miRNA)在多个生物学过程中发挥作用,其在体液中的水平与包括不同类型癌症在内的各种疾病的发病机制相关。因此,miRNA被认为是很有前景的诊断生物标志物候选物,能够实现病理发病的早期检测以及在治疗期间监测药物反应。然而,当前用于miRNA定量的方法,如Northern印迹法、等温扩增法、逆转录聚合酶链反应(RT-PCR)、微阵列法和下一代测序法,受到依赖集中实验室、成本高以及需要专业人员的限制。因此,非常需要开发用于miRNA检测的灵敏、简单且一步到位的分析技术,特别是考虑到癌症早期诊断和及时治疗的重要性。侧向流动分析(LFA)是医疗保健应用中最具吸引力的即时检测(POC)设备之一。这些系统允许使用广泛受众都能使用的低成本设置快速直接地检测分析物。本综述重点关注基于LFA的用于检测和定量与各种癌症诊断相关的miRNA的方法,特别强调通过应用不同标记和检测系统实现的灵敏度提高。通过定量定制生物标志物对这些疾病进行早期、非侵入性检测可显著降低死亡率、提高生存率并降低治疗成本。