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Nucleic Acid Amplification Circuit-Based Hydrogel (NACH) Assay for One-Step Detection of Metastatic Gastric Cancer-Derived Exosomal miRNA

Authors
 Seung Beom Seo  ;  Jaewoo Lim  ;  Kyujung Kim  ;  Inhee Maeng  ;  Hyun Wook Rho  ;  Hye Young Son  ;  Eunjung Kim  ;  Eunji Jang  ;  Taejoon Kang  ;  Juyeon Jung  ;  Seung Jae Oh  ;  Yong-Min Huh  ;  Eun-Kyung Lim 
Citation
 ADVANCED SCIENCE, Vol.11(43) : e2407621, 2024-11 
Journal Title
ADVANCED SCIENCE
ISSN
 * 
Issue Date
2024-11
MeSH
Animals ; Biomarkers, Tumor / genetics ; Epithelial-Mesenchymal Transition / genetics ; Exosomes* / genetics ; Exosomes* / metabolism ; Humans ; Hydrogels* / chemistry ; Mice ; MicroRNAs* / genetics ; Nucleic Acid Amplification Techniques* / methods ; Stomach Neoplasms* / diagnosis ; Stomach Neoplasms* / genetics ; Stomach Neoplasms* / pathology
Keywords
exosomal miRNA ; gastric cancer ; hydrogel assay ; nucleic acid amplification circuit ; portable fluorometer
Abstract
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.
Files in This Item:
T202501080.pdf Download
DOI
10.1002/advs.202407621
Appears in Collections:
1. College of Medicine (의과대학) > Research Institute (부설연구소) > 1. Journal Papers
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiology (영상의학교실) > 1. Journal Papers
Yonsei Authors
Maeng, In hee(맹인희)
Son, Hye Young(손혜영) ORCID logo https://orcid.org/0000-0001-5977-6784
Oh, Seung Jae(오승재)
Huh, Yong Min(허용민) ORCID logo https://orcid.org/0000-0002-9831-4475
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/204606
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