Bionanotechnology Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, 34141, Republic of Korea.
Department of Cogno-Mechatronics Engineering, Pusan National University, Pusan, 46241, Republic of Korea.
Adv Sci (Weinh). 2024 Nov;11(43):e2407621. doi: 10.1002/advs.202407621. Epub 2024 Sep 23.
Gastric cancer (GC) is recognized as the fifth most prevalent malignant tumor worldwide. It is characterized by diverse clinical symptoms, treatment responses, and prognoses. In GC prognosis, the promotion of epithelial-mesenchymal transition (EMT) fosters cancer cell invasion and metastasis, thereby triggering the dissemination of tumor cells. This study proposes a nucleic acid amplification circuit-based hydrogel (NACH) assay for identifying exosomal miRNA derived from metastatic GC. The NACH assay employs the rolling circle amplification method and targets miRNA-21, a tumor-related oncogene, and miRNA-99a, which promotes EMT. Specific amplification probes for each target are immobilized within the hydrogel, enabling a streamlined, one-step amplification reaction. The NACH assay exhibits a detection limit of 1 fm for miRNA-21 and miRNA-99a, thereby enabling rapid and highly sensitive on-site detection. Performance evaluation using exosomal miRNA extracted from cell culture media, mouse plasma, and human plasma revealed fluorescence intensity patterns similar to those obtained in qRT-PCR. Furthermore, deploying a custom-developed portable fluorometer for the NACH assay allows for diagnostic performance assessment and point-of-care testing using clinical samples from GC patients. These findings emphasize the potential of the NACH assay to be used as a robust tool for the genetic diagnosis of GC based on exosome detection.
胃癌(GC)是全球第五大常见恶性肿瘤。其具有多样化的临床症状、治疗反应和预后。在 GC 预后中,上皮-间充质转化(EMT)的促进促进了癌细胞的侵袭和转移,从而引发肿瘤细胞的扩散。本研究提出了一种基于核酸扩增电路的水凝胶(NACH)检测方法,用于鉴定转移性 GC 来源的外泌体 miRNA。NACH 检测法采用滚环扩增方法,针对肿瘤相关致癌基因 miRNA-21 和促进 EMT 的 miRNA-99a 进行检测。每个靶标都有特异性的扩增探针固定在水凝胶内,实现了简化的一步式扩增反应。NACH 检测法对 miRNA-21 和 miRNA-99a 的检测限分别为 1 fM,从而实现了快速和高度灵敏的现场检测。使用细胞培养介质、小鼠血浆和人血浆中提取的外泌体 miRNA 进行性能评估,得到的荧光强度模式与 qRT-PCR 相似。此外,使用专门开发的便携式荧光计进行 NACH 检测法,可对 GC 患者的临床样本进行诊断性能评估和即时检测。这些发现强调了 NACH 检测法作为基于外泌体检测的 GC 遗传诊断的强大工具的潜力。