卵巢癌
癌症研究
恶性肿瘤
癌症
癌细胞
细胞培养
细胞外小泡
纳米粒子跟踪分析
表面增强拉曼光谱
小泡
细胞
拉曼光谱
化学
病理
生物
医学
细胞生物学
内科学
膜
生物化学
微泡
拉曼散射
遗传学
基因
物理
小RNA
光学
作者
Nina M. Ćulum,Tyler T. Cooper,Gilles Lajoie,Thamara Dayarathna,Stephen Pasternak,Jiahui Liu,Yangxin Fu,Lynne‐Marie Postovit,François Lagugné‐Labarthet
出处
期刊:Analyst
[Royal Society of Chemistry]
日期:2021-01-01
卷期号:146 (23): 7194-7206
被引量:37
摘要
Ovarian cancer is the most lethal gynecological malignancy, owing to the fact that most cases are diagnosed at a late stage. To improve prognosis and reduce mortality, we must develop methods for the early diagnosis of ovarian cancer. A step towards early and non-invasive cancer diagnosis is through the utilization of extracellular vesicles (EVs), which are nanoscale, membrane-bound vesicles that contain proteins and genetic material reflective of their parent cell. Thus, EVs secreted by cancer cells can be thought of as cancer biomarkers. In this paper, we present gold nanohole arrays for the capture of ovarian cancer (OvCa)-derived EVs and their characterization by surface-enhanced Raman spectroscopy (SERS). For the first time, we have characterized EVs isolated from two established OvCa cell lines (OV-90, OVCAR3), two primary OvCa cell lines (EOC6, EOC18), and one human immortalized ovarian surface epithelial cell line (hIOSE) by SERS. We subsequently determined their main compositional differences by principal component analysis and were able to discriminate the groups by a logistic regression-based machine learning method with ∼99% accuracy, sensitivity, and specificity. The results presented here are a great step towards quick, facile, and non-invasive cancer diagnosis.
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