A specific spectral signature of serum and plasma-derived extracellular vesicles for cancer screening

被引:73
作者
Krafft, Christoph [1 ]
Wilhelm, Konrad [2 ,3 ]
Eremin, Anna [3 ]
Nestel, Sigrun [4 ]
von Bubnoff, Nikolas [5 ,6 ,7 ]
Schultze-Seemann, Wolfgang [2 ]
Popp, Juergen [1 ]
Nazarenko, Irina [3 ]
机构
[1] Leibniz Inst Photon Technol, Jena, Germany
[2] Univ Freiburg, Med Ctr, Ctr Surg, Dept Urol, Freiburg, Germany
[3] Univ Freiburg, Fac Med, Med Ctr, Inst Environm Hlth Sci & Hosp Infect Control, Freiburg, Germany
[4] Univ Freiburg, Inst Anat & Cell Biol, Freiburg, Germany
[5] Univ Freiburg, Med Ctr, Dept Hematol Oncol & Stem Cell Transplantat, Freiburg, Germany
[6] DKTK, German Canc Consortium, Heidelberg, Germany
[7] DKFZ, German Canc Res Ctr, Heidelberg, Germany
关键词
Nanomedicine; Minimal- and non-invasive diagnostics; Extracellular vesicles; Exosomes; Raman spectroscopy; Infrared spectroscopy; ENHANCED RAMAN-SPECTROSCOPY; PROSTATE;
D O I
10.1016/j.nano.2016.11.016
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In cancer, extracellular vesicles (EV) contribute to tumor progression by regulating local and systemic effects. Being released into body fluids, EV may be used in nanomedicine as a valuable source for diagnostic biomarkers. In this work, infrared and Raman spectroscopy were used for comprehensive comparative analysis of cancer versus non-cancer EV and patient screening. Two different EV fractions enriched in exosomes and microvesicles were isolated by differential centrifugation from serum and plasma of cancer and non-cancer patients and from serum and plasma of a healthy donor. The EV fractions were then subjected to drop-coating deposition and drying on calcium fluoride substrates. Reduction of alpha-helix-rich proteins and enhancement of beta-sheet-rich proteins as a cancer-specific blood EV signature was determined, and subsequently this feature was applied for a pilot study aiming to detect prostate cancer in a test cohort of patients with high-grade prostate carcinoma and benign hypoplasia. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:835 / 841
页数:7
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