胰腺癌
外体
生物标志物
液体活检
微泡
医学
癌症
活检
癌症生物标志物
阶段(地层学)
癌症研究
病理
内科学
化学
小RNA
生物
生物化学
古生物学
基因
作者
Zhiguo Yu,Yang� Yang,Wenming Fang,Ping Hu,Yingbin Liu,Jianlin Shi
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-06-08
卷期号:17 (12): 11384-11395
被引量:23
标识
DOI:10.1021/acsnano.3c00674
摘要
Pancreatic cancer, with extremely limited treatment options and poor prognosis, urgently needs a breakthrough in early diagnosis and monitoring. Tumor exosomes (T-Exos) detection is presently one of the most clinically significant liquid biopsy approaches for non-invasive pancreatic cancer early diagnosis, which, unfortunately, cannot be applied as a routine diagnostic tool until a number of obstacles, such as unsatisfactory specificity and sensitivity, as well as labor-intensive purification and analysis procedures by ultracentrifugation and enzyme-linked immunosorbent assay, are overcome. Here, we report a facile nanoliquid biopsy assay for the especially specific, ultrasensitive yet economical T-Exos detection by a dual specific biomarker antigen co-recognition and capturing strategy, which is enabled by grafting two corresponding capture antibodies on magnetic nanoparticles and gold nanoparticles, for the accurate detection of target tumor exosomes. This approach exhibits excellent specificity and ultrahigh sensitivity of detecting as low as 78 pg/mL pancreatic cancer exosome specific protein GPC1. Successful screening of 21 pancreatic cancer samples from 22 normal control cases with the enhanced specificity and sensitivity ensures the promising non-invasive monitoring and diagnosis for early stage pancreatic cancer.
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