Extracellular Vesicles in Renal Cell Carcinoma: Multifaceted Roles and Potential Applications Identified by Experimental and Computational Methods

被引:23
作者
Qin, Zhiyuan [1 ]
Xu, Qingwen [1 ]
Hu, Haihong [1 ]
Yu, Lushan [1 ]
Zeng, Su [1 ]
机构
[1] Zhejiang Univ, Inst Drug Metab & Pharmaceut Anal, Coll Pharmaceut Sci, Hangzhou, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2020年 / 10卷
基金
国家重点研发计划;
关键词
renal cell carcinoma; extracellular vesicles; exosomes; biomarkers; drug targets; drug vehicles; artificial intelligence; machine learning; EXOSOME-MEDIATED TRANSFER; STEM-CELLS; PROMISING BIOMARKER; MESSENGER-RNA; CANCER; DATABASE; MICROVESICLES; SECRETION; BIOGENESIS; DIAGNOSIS;
D O I
10.3389/fonc.2020.00724
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Renal cell carcinoma (RCC) is the most common type of kidney cancer. Increasingly evidences indicate that extracellular vesicles (EVs) orchestrate multiple processes in tumorigenesis, metastasis, immune evasion, and drug response of RCC. EVs are lipid membrane-bound vesicles in nanometer size and secreted by almost all cell types into the extracellular milieu. A myriad of bioactive molecules such as RNA, DNA, protein, and lipid are able to be delivered via EVs for the intercellular communication. Hence, the abundant content of EVs is appealing reservoir for biomarker identification through computational analysis and experimental validation. EVs with excellent biocompatibility and biodistribution are natural platforms that can be engineered to offer achievable drug delivery strategies for RCC therapies. Moreover, the multifaceted roles of EVs in RCC progression also provide substantial targets and facilitate EVs-based drug discovery, which will be accelerated by using artificial intelligence approaches. In this review, we summarized the vital roles of EVs in occurrence, metastasis, immune evasion, and drug resistance of RCC. Furthermore, we also recapitulated and prospected the EVs-based potential applications in RCC, including biomarker identification, drug vehicle development as well as drug target discovery.
引用
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页数:15
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