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The potential role of exosomes derived from ovarian cancer cells for diagnostic and therapeutic approaches

Authors
Yang, ChangwonKim, Hee SeungSong, GwonhwaLim, Whasun
Issue Date
Dec-2019
Publisher
WILEY
Keywords
biomarker; exosome; microenvironment; microRNA; ovarian cancer cells
Citation
JOURNAL OF CELLULAR PHYSIOLOGY, v.234, no.12, pp.21493 - 21503
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF CELLULAR PHYSIOLOGY
Volume
234
Number
12
Start Page
21493
End Page
21503
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/61477
DOI
10.1002/jcp.28905
ISSN
0021-9541
Abstract
Most patients with ovarian cancer (OC) are diagnosed at the advanced stages due to the absence of appropriate early diagnostic markers. Thus, OC is a gynecological disease with a low-survival rate. Exosomes are extracellular vesicles that are widely being considered as mediators for the noninvasive diagnosis of OC. Exosomes are expected to aid in the effective diagnosis of OC because they carry components, such as RNAs, proteins, and lipids, the compositions of which vary depending on the pathological characteristics of the patient. In this review, we document the methods that have been developed to detect exosomes and their components in OC. We also assess the potential biomarkers contained in exosomes that could be clinically useful, such as proteins, microRNAs (miRNAs), long noncoding RNAs (lncRNAs), and phospholipids. Moreover, we described the role played by exosomes in the tumor microenvironment and in OC angiogenesis, migration, and tumor growth. Various types of cells in the tumor microenvironment, including macrophages, fibroblasts, and mesenchymal stem cells (MSCs), interact directly with exosomes and promote or inhibit the progression of OC. Therefore, we summarize the studies that have suggested a therapeutic approach to OC using exosomes. Collectively, understanding the mechanism of exosome-based OC progression would broaden our knowledge regarding the diagnosis and therapy of OC.
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