Multi-targeted nanoarrays for early broad-spectrum detection of lung cancer based on blood biopsy of tumor exosomes

微泡 肺癌 液体活检 生物标志物 适体 癌症 循环肿瘤细胞 癌症研究 靶向治疗 癌症生物标志物 癌细胞 化学 流式细胞术 小RNA 病理 免疫学 分子生物学 生物 医学 转移 内科学 基因 生物化学
作者
Shu Lian,Qixuan Wang,Yuxin Liu,Yusheng Lu,Lu Huang,Hao‐Hua Deng,Xiaodong Xie
出处
期刊:Talanta [Elsevier BV]
卷期号:276: 126270-126270
标识
DOI:10.1016/j.talanta.2024.126270
摘要

Liquid biopsies utilizing tumor exosomes offer a noninvasive approach for cancer diagnosis. However, validation studies consistently report that in the early stages of cancer, the secretion of exosomes by cancer cells is relatively low, while bodily fluids exhibit a high abundance of other interfering biomolecules. Additionally, target mutations or differences in biomarker expression among various lung cancer subtypes may contribute to detection failures. In this study, we propose a targeted nanoarray-based early cancer diagnostic approach for multiple subtypes of lung cancer. The targeted nanoarray was constructed by modifying five targeting aptamers onto mesoporous silica nanoparticles through the conjugation between amino and carboxyl groups. The flow cytometry experiments demonstrated the specific recognition ability of the targeted nanoarray to tumor exosomes in PBS, even at biomarker expression levels as low as 1.5%. Moreover, the TEM results indicated that the targeted nanoarray could isolate tumor exosomes in the blood of tumor-bearing mice. Furthermore, the targeted nanoarray could detect tumor exosomes in the blood of various lung cancer bearing mice, including at the early stages of cancer, which has just been established for 7 days. Overall, the targeted nanoarray represents a promising tool for the early detection of various subtypes of lung cancer.
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