Early-Stage Lung Cancer Diagnosis by Deep Learning-Based Spectroscopic Analysis of Circulating Exosomes

微泡 液体活检 肺癌 癌症 外体 医学 癌症研究 肿瘤科 活检 病理 小RNA 阶段(地层学) 内科学 生物 生物化学 古生物学 基因
作者
Hyunku Shin,Seunghyun Oh,Soonwoo Hong,Min-Sung Kang,Daehyeon Kang,Yong-gu Ji,Byeong Hyeon Choi,Ka‐Won Kang,Hyesun Jeong,Yong Park,Sunghoi Hong,Hyun Koo Kim,Yeonho Choi
出处
期刊:ACS Nano [American Chemical Society]
卷期号:14 (5): 5435-5444 被引量:486
标识
DOI:10.1021/acsnano.9b09119
摘要

Lung cancer has a high mortality rate, but an early diagnosis can contribute to a favorable prognosis. A liquid biopsy that captures and detects tumor-related biomarkers in body fluids has great potential for early-stage diagnosis. Exosomes, nanosized extracellular vesicles found in blood, have been proposed as promising biomarkers for liquid biopsy. Here, we demonstrate an accurate diagnosis of early-stage lung cancer, using deep learning-based surface-enhanced Raman spectroscopy (SERS) of the exosomes. Our approach was to explore the features of cell exosomes through deep learning and figure out the similarity in human plasma exosomes, without learning insufficient human data. The deep learning model was trained with SERS signals of exosomes derived from normal and lung cancer cell lines and could classify them with an accuracy of 95%. In 43 patients, including stage I and II cancer patients, the deep learning model predicted that plasma exosomes of 90.7% patients had higher similarity to lung cancer cell exosomes than the average of the healthy controls. Such similarity was proportional to the progression of cancer. Notably, the model predicted lung cancer with an area under the curve (AUC) of 0.912 for the whole cohort and stage I patients with an AUC of 0.910. These results suggest the great potential of the combination of exosome analysis and deep learning as a method for early-stage liquid biopsy of lung cancer.
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