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Comparison Study of Small Extracellular Vesicle Isolation Methods for Profiling Protein Biomarkers in Breast Cancer Liquid Biopsies
被引:3
|作者:
Lee, Yujin
[1
,2
]
Ni, Jie
[1
,2
]
Wasinger, Valerie C.
[3
]
Graham, Peter
[1
,2
]
Li, Yong
[1
,2
]
机构:
[1] UNSW Sydney, Sch Clin Med, St George & Sutherland Clin Campuses, Kensington, NSW 2052, Australia
[2] St George Hosp, Canc Care Ctr, Kogarah, NSW 2217, Australia
[3] UNSW Sydney, Mark Wainwright Analyt Ctr, Bioanalyt Mass Spectrometry Facil, Kensington, NSW 2052, Australia
关键词:
breast cancer;
extracellular vesicle;
biomarker;
diagnosis;
isolation;
liquid biopsy;
HUMAN SERUM;
EXOSOMES;
EXPRESSION;
SECRETION;
OBESITY;
RNA;
D O I:
10.3390/ijms242015462
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Small extracellular vesicles (sEVs) are an important intercellular communicator, participating in all stages of cancer metastasis, immunity, and therapeutic resistance. Therefore, protein cargoes within sEVs are considered as a superior source for breast cancer (BC) biomarker discovery. Our study aimed to optimise the approach for sEV isolation and sEV proteomic analysis to identify potential sEV protein biomarkers for BC diagnosis. sEVs derived from BC cell lines, BC patients' plasma, and non-cancer controls were isolated using ultracentrifugation (UC), a Total Exosome Isolation kit (TEI), and a combined approach named UCT. In BC cell lines, the UC isolates showed a higher sEV purity and marker expression, as well as a higher number of sEV proteins. In BC plasma samples, the UCT isolates showed the highest proportion of sEV-related proteins and the lowest percentage of lipoprotein-related proteins. Our data suggest that the assessment of both the quantity and quality of sEV isolation methods is important in selecting the optimal approach for the specific sEV research purpose, depending on the sample types and downstream analysis.
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