乳腺癌
化学
细胞外小泡
适体
转移
整合素
肿瘤进展
癌症
循环肿瘤细胞
纳米粒子跟踪分析
癌症研究
癌细胞
纳米技术
分子生物学
细胞
微泡
细胞生物学
生物化学
基因
材料科学
内科学
医学
生物
小RNA
作者
Haozhi Lei,Haoze Wang,X D Wang,Zeyu Xiao,Tian Tian,Kai Cui
出处
期刊:Talanta
[Elsevier BV]
日期:2024-04-16
卷期号:275: 126092-126092
被引量:6
标识
DOI:10.1016/j.talanta.2024.126092
摘要
Detection of progression is of great importance to breast cancer treatment and can benefit patients. Limited by current detection technologies and biomarkers, early breast cancer progression diagnosis remains challenging. Researchers have found blood extracellular vesicles (EVs)-derived integrin α6β4 directly facilitate progression in breast cancer, enabling cancer detection. However, EVs size and heterogeneity hinder protein detection, masked by abundant background EVs. Hence, novel tools for efficient detection of EVs with high selectivity and low interference are significantly desired. Here, a new silver-coated gold nanorods SERS probe, termed as Au@Ag@IDA-B/4MSTP, based on DNA aptamer was established for the detection of integrin α6β4 derived from EVs. Validation of the Au@Ag@IDA-B/4MSTP probes using cell-culture-derived EVs revealed a LOD of 23 particles/μL for EVs detection. This tool was further confirmed to mimic the real state of cancer with subcutaneous tumor model and lung metastasis model in mice. With 10 μL of blood plasma and simple Raman analysis process, the test achieved 85.7 % sensitivity and 83.3 % specificity. Moreover, our method achieves a simplified approach that expedites the detection process. These results demonstrate the good detection performance of Au@Ag@IDA-B/4MSTP probes for EVs integrin α6β4, and suggest that this non-invasive approach could be a promising tool for early detection of breast cancer progression.
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