Urinary exosomal mRNA detection using novel isothermal gene amplification method based on three-way junction

2020 ◽  
Vol 167 ◽  
pp. 112474 ◽  
Author(s):  
Jeong Moon ◽  
Jaewoo Lim ◽  
Seoyoung Lee ◽  
Hye Young Son ◽  
Hyun Wook Rho ◽  
...  
2020 ◽  
Vol 12 (46) ◽  
pp. 5551-5561
Author(s):  
Tianzeng Huang ◽  
Linzhi Li ◽  
Xing Liu ◽  
Qi Chen ◽  
Xueen Fang ◽  
...  

LAMP is a relatively novel gene amplification method under isothermal conditions with rapidity, and high specificity. It is widely applied in the field of food safety, such as in the detection of foodborne pathogens, GM, OP pesticides and so on


2019 ◽  
Vol 15 (3) ◽  
pp. 399-403 ◽  
Author(s):  
Junji Hosokawa-Muto ◽  
Hiroki Sakai ◽  
Yukiko Sassa ◽  
Yoshihito Fujinami ◽  
Mai Kishimoto ◽  
...  

2007 ◽  
Vol 142 (2) ◽  
pp. 283-292 ◽  
Author(s):  
T. Uemori ◽  
H. Mukai ◽  
O. Takeda ◽  
M. Moriyama ◽  
Y. Sato ◽  
...  

2011 ◽  
Vol 80 (1) ◽  
pp. 41-46 ◽  
Author(s):  
Hiromitsu Yoshimura ◽  
Shingo Sekine ◽  
Hisashi Adachi ◽  
Yoshikatsu Uematsu ◽  
Akiko Mitani ◽  
...  

2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Hongxia Li ◽  
Antony R. Warden ◽  
Wenqiong Su ◽  
Jie He ◽  
Xiao Zhi ◽  
...  

AbstractPancreatic cancer, at unresectable advanced stages, presents poor prognoses, which could be prevented by early pancreatic cancer diagnosis methods. Recently, a promising early-stage pancreatic cancer biomarker, extracellular vesicles (EVs) related glypican-1 (GPC1) mRNA, is found to overexpress in pancreatic cancer cells. Current mRNA detection methods usually require expensive machinery, strict preservation environments, and time-consuming processes to guarantee detection sensitivity, specificity, and stability. Herein, we propose a novel two-step amplification method (CHAGE) via the target triggered Catalytic Hairpin Assembly strategy combined with Gold-Enhanced point-of-care-testing (POCT) technology for sensitive visual detection of pancreatic cancer biomarker. First, utilizing the catalyzed hairpin DNA circuit, low expression of the GPC1 mRNA was changed into amplification product 1 (AP1, a DNA duplex) as the next detection targets of the paper strips. Second, the AP1 was loaded onto a lateral flow assay and captured with the gold signal nanoparticles to visualize results. Finally, the detected results can be further enhanced by depositing gold to re-enlarge the sizes of gold nanoparticles in detection zones. As a result, the CHAGE methodology lowers the detection limit of mRNA to 100 fM and provides results within 2 h at 37 °C. Furthermore, we demonstrate the successful application in discriminating pancreatic cancer cells by analyzing EVs’ GPC1 mRNA expression levels. Hence, the CHAGE methodology proposed here provides a rapid and convenient POCT platform for sensitive detection of mRNAs through unique probes designs (COVID, HPV, etc.).


PLoS ONE ◽  
2012 ◽  
Vol 7 (7) ◽  
pp. e41787 ◽  
Author(s):  
Yoshio Araki ◽  
Tetsuro Hamafuji ◽  
Chiemi Noguchi ◽  
Noriaki Shimizu

2014 ◽  
Vol 201 ◽  
pp. 31-37 ◽  
Author(s):  
Takao Segawa ◽  
Yuki Kobayashi ◽  
Yukina Sase ◽  
Takuya Itou ◽  
Miwa Suzuki ◽  
...  

1989 ◽  
Vol 162 (2) ◽  
pp. 664-672 ◽  
Author(s):  
Wataru Sato ◽  
Masashi Tanaka ◽  
Kinji Ohno ◽  
Tomoko Yamamoto ◽  
Goro Takada ◽  
...  

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