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

Journal: ACS nano
Published Date:

Abstract

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.

Authors

  • Hyunku Shin
    Department of Bio-convergence Engineering, Korea University, Seoul 02841, Republic of Korea.
  • Seunghyun Oh
    School of Biomedical Engineering, Korea University, Seoul 02841, Republic of Korea.
  • Soonwoo Hong
    Department of Bio-convergence Engineering, Korea University, Seoul 02841, Republic of Korea.
  • Minsung Kang
    Department of Bioengineering, Korea University, Seoul 02841, Republic of Korea.
  • Daehyeon Kang
    School of Biomedical Engineering, Korea University, Seoul 02841, Republic of Korea.
  • Yong-Gu Ji
    Exopert Corporation, Seoul 02841, Republic of Korea.
  • Byeong Hyeon Choi
    Department of Biomedical Sciences, College of Medicine, Korea University, Seoul 02841, Republic of Korea.
  • Ka-Won Kang
    Division of Hematology-Oncology, Department of Internal Medicine, Korea University College of Medicine, Seoul 02841, Republic of Korea.
  • Hyesun Jeong
    School of Biosystems and Biomedical Sciences, Korea University, Seoul 02841, Republic of Korea.
  • Yong Park
    Division of Hematology-Oncology, Department of Internal Medicine, Korea University College of Medicine, Seoul 02841, Republic of Korea.
  • Sunghoi Hong
    School of Biosystems and Biomedical Sciences, Korea University, Seoul 02841, Republic of Korea.
  • Hyun Koo Kim
    Department of Biomedical Sciences, College of Medicine, Korea University, Seoul 02841, Republic of Korea.
  • Yeonho Choi
    Department of Bio-convergence Engineering, Korea University, Seoul 02841, Republic of Korea.