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Feasibility of Raman spectroscopic identification of gall bladder cancer using extracellular vesicles extracted from bile

Authors
Bui, Thu ThuyJang, EunjinShin, Ji HyunKim, Tae HunKim, HayoonChoi, DonghoVu, Tung DuyChung, Hoeil
Issue Date
Jul-2023
Publisher
Royal Society of Chemistry
Citation
Analyst, v.148, no.17, pp.4156 - 4165
Indexed
SCIE
SCOPUS
Journal Title
Analyst
Volume
148
Number
17
Start Page
4156
End Page
4165
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/192965
DOI
10.1039/d3an00806a
ISSN
0003-2654
Abstract
Extracellular vesicles (EVs), which are heterogeneous membrane-based vesicles with bilayer cell membrane structures, could be versatile biomarkers for the identification of diverse diseases including cancers. With this potential, this study has attempted the Raman spectroscopic identification of gall bladder (GB) cancer by directly measuring the EV solution extracted from human bile without further sample drying. For this purpose, bile samples were obtained from four normal individuals and 21 GB polyp, eight hepatocellular carcinoma (HCC), and five GB cancer patients, and EVs were extracted from each of the bile samples. The Raman peak shapes of the EVs extracted from the GB cancer samples, especially the relative intensities of peaks in the 1560-1340 cm−1 range, were dissimilar to those of the samples from the normal, GB polyp, and HCC groups. The intensity ratios of peaks at 1537 and 1453 cm−1 and at 1395 and 1359 cm−1 of the GB cancer samples were lower and higher, respectively, than those of the samples of the remaining three groups. The differences of peak intensity ratios were statistically significant based on the Mann-Whitney U test. DNA/RNA bases, amino acids, and bile salts contributed to the spectra of EVs, and their relative abundances seemed to vary according to the occurrence of GB cancer. The varied metabolite compositions and/or structures of EVs were successfully demonstrated by the dissimilar peak intensity ratios in the Raman spectra, thereby enabling the discrimination of GB cancer.
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