Comparative Proteomic Analysis of Exosomes and Microvesicles in Human Saliva for Lung Cancer

Extracellular vesicles (EVs) are cell-derived microparticles present in most body fluids, mainly including microvesicles and exosomes. EV-harbored proteins have emerged as novel biomarkers for the diagnosis and prediction of different cancers. We successfully isolated microvesicles and exosomes from...

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Published inJournal of proteome research Vol. 17; no. 3; pp. 1101 - 1107
Main Authors Sun, Yan, Huo, Chunhui, Qiao, Zhi, Shang, Zhi, Uzzaman, Asad, Liu, Sha, Jiang, Xiaoteng, Fan, Liu-Yin, Ji, Liyun, Guan, Xin, Cao, Cheng-Xi, Xiao, Hua
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 02.03.2018
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Summary:Extracellular vesicles (EVs) are cell-derived microparticles present in most body fluids, mainly including microvesicles and exosomes. EV-harbored proteins have emerged as novel biomarkers for the diagnosis and prediction of different cancers. We successfully isolated microvesicles and exosomes from human saliva, which were further characterized comprehensively. Salivary EV protein profiling in normal subjects and lung cancer patients was systematically compared through utilizing LC–MS/MS-based label-free quantification. 785 and 910 proteins were identified from salivary exosomes and microvesicles, respectively. According to statistical analysis, 150 and 243 proteins were revealed as dysregulated candidates in exosomes and microvesicles for lung cancer. Among them, 25 and 40 proteins originally from distal organ cells were found in the salivary exosomes and microvesicles of lung cancer patients. In particular, 5 out of 25 and 9 out of 40 are lung-related proteins. Six potential candidates were selected for verification by Western blot, and four of them, namely, BPIFA1, CRNN, MUC5B, and IQGAP, were confirmed either in salivary microvesicles or in exosomes. Our data collectively demonstrate that salivary EVs harbor informative proteins that might be used for the detection of lung cancer through a noninvasive way.
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ISSN:1535-3893
1535-3907
1535-3907
DOI:10.1021/acs.jproteome.7b00770