Peng Weipan, Shi Mengting, Hu Bin, Jia Jingyu, Li Xinyue, Wang Nan, Man Shuli, Ye Shengying, Ma Long
State Key Laboratory of Food Nutrition and Safety, Key Laboratory of Industrial Microbiology, Tianjin Key Laboratory of Industry Microbiology, International China International Science and Technology Cooperation Base of Food Nutrition/Safety and Medicinal Chemistry, College of Biotechnology, Ministry of Education, National and Local United Engineering Lab of Metabolic Control Fermentation Technology, Tianjin University of Science & Technology, Tianjin, 300457, China.
Department of Pharmacy, The First Affiliated Hospital, College of Clinical Medicine, Henan University of Science and Technology, Luoyang, 471003, China.
Mol Cancer. 2025 Mar 14;24(1):78. doi: 10.1186/s12943-024-02222-5.
As promising noninvasive biomarkers, nucleic acids provide great potential to innovate cancer early detection methods and promote subsequent diagnosis to improve the survival rates of patient. Accurate, straightforward and sensitive detection of such nucleic acid-based cancer biomarkers in complex biological samples holds significant clinical importance. However, the low abundance creates huge challenges for their routine detection. As the next-generation diagnostic tool, Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein (Cas) with their high programmability, sensitivity, fidelity, single-base resolution, and precise nucleic acid positioning capabilities are extremely attractive for trace nucleic acid-based cancer biomarkers (NABCBs), permitting rapid, ultra-sensitive and specific detection. More importantly, by combing with nanotechnology, it can solve the long-lasting problems of poor sensitivity, accuracy and simplicity, as well as to achieve integrated miniaturization and portable point-of-care testing (POCT) detection. However, existing literature lacks specific emphasis on this topic. Thus, we intend to propose a timely one for the readers. This review will bridge this gap by providing insights for CRISPR/Cas-based nano-biosensing development and highlighting the current state-of-art, challenges, and prospects. We expect that it can provide better understanding and valuable insights for trace NABCBs detection, thereby facilitating advancements in early cancer screening/detection/diagnostics and win practical applications in the foreseeable future.
作为有前景的非侵入性生物标志物,核酸为创新癌症早期检测方法和推动后续诊断以提高患者生存率提供了巨大潜力。在复杂生物样本中准确、直接且灵敏地检测此类基于核酸的癌症生物标志物具有重大临床意义。然而,低丰度给它们的常规检测带来了巨大挑战。作为下一代诊断工具,成簇规律间隔短回文重复序列(CRISPR)/CRISPR相关蛋白(Cas)凭借其高可编程性、灵敏度、保真度、单碱基分辨率和精确的核酸定位能力,对于基于痕量核酸的癌症生物标志物(NABCBs)极具吸引力,能够实现快速、超灵敏且特异的检测。更重要的是,通过与纳米技术相结合,它可以解决长期存在的灵敏度差、准确性低和操作不简便等问题,以及实现集成微型化和便携式即时检测(POCT)。然而,现有文献对此主题缺乏具体强调。因此,我们打算为读者及时提出这样一个主题。本综述将通过提供基于CRISPR/Cas的纳米生物传感发展的见解,并突出当前的技术水平、挑战和前景来弥补这一差距。我们期望它能为痕量NABCBs检测提供更好的理解和有价值的见解,从而推动早期癌症筛查/检测/诊断的进展,并在可预见的未来赢得实际应用。