Fu Youlin, Zhang Peng, Chen Feng, Xie Ziqiang, Xiao Shihui, Huang Zhihao, Lau Cia-Hin, Zhu Haibao, Luo Jun
Department of Cardiology, Ganzhou People's Hospital, Ganzhou, Jiangxi, China.
Department of Biology, College of Science, Shantou University, Shantou, 515063, Guangdong, China.
Mol Biol Rep. 2025 Jan 11;52(1):114. doi: 10.1007/s11033-024-10205-4.
As multiple imaging modalities cannot reliably diagnose cardiac tumors, the molecular approach offers alternative ways to detect rare ones. One such molecular approach is CRISPR-based diagnostics (CRISPR-Dx). CRISPR-Dx enables visual readout, portable diagnostics, and rapid and multiplex detection of nucleic acids such as microRNA (miRNA). Dysregulation of miRNA expressions has been associated with cardiac tumors such as atrial myxoma and angiosarcoma. Diverse CRISPR-Dx systems have been developed to detect miRNA in recent years. These CRISPR-Dx systems are generally classified into four classes, depending on the Cas proteins used (Cas9, Cas12, Cas13, or Cas12f). CRISPR/Cas systems are integrated with various isothermal amplifications to detect low-abundance miRNAs. Amplification-free CRISPR-Dx systems have also been recently developed to detect miRNA directly. Herein, we critically discuss the advances, pitfalls, and future perspectives for these CRISPR-Dx systems in detecting miRNA, focusing on the diagnosis and prognosis of cardiac tumors.
由于多种成像方式无法可靠地诊断心脏肿瘤,分子方法为检测罕见肿瘤提供了替代途径。一种这样的分子方法是基于CRISPR的诊断(CRISPR-Dx)。CRISPR-Dx能够实现可视化读数、便携式诊断以及对核酸(如微小RNA(miRNA))的快速多重检测。miRNA表达失调与心房黏液瘤和血管肉瘤等心脏肿瘤有关。近年来,已开发出多种用于检测miRNA的CRISPR-Dx系统。根据所使用的Cas蛋白(Cas9、Cas12、Cas13或Cas12f),这些CRISPR-Dx系统通常分为四类。CRISPR/Cas系统与各种等温扩增技术相结合,以检测低丰度miRNA。最近还开发了无需扩增的CRISPR-Dx系统来直接检测miRNA。在此,我们批判性地讨论这些CRISPR-Dx系统在检测miRNA方面的进展、缺陷和未来前景,重点关注心脏肿瘤的诊断和预后。