Extracellular vesicles in liquid biopsies: there is hope for oral squamous cell carcinoma

被引:0
|
作者
Leung, Leanne Lee [1 ]
Qu, Xinyu [1 ]
Chen, Bojie [1 ]
Chan, Jason YK. [1 ]
机构
[1] Chinese Univ Hong Kong, Dept Otorhinolaryngol Head & Neck Surg, Hong Kong 00000, Peoples R China
关键词
Oral cancer; liquid biopsy; saliva; plasma/serum; lymphatic fluid; EVs; extracellular vesicles; EXOSOMAL MICRORNAS; LICHEN-PLANUS; NODE BIOPSY; CANCER-RISK; MANAGEMENT; DRAINAGE; PLASMA; FLUID; HEAD;
D O I
10.20517/evcna.2024.29
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
Current approaches to oral cancer diagnosis primarily involve physical examination, tissue biopsy, and advanced computer-aided imaging techniques. However, despite these advances, patient survival rates have not significantly improved. Hence, there is a critical need to develop minimally invasive tools with high sensitivity and specificity to improve patient survival and quality of life. Liquid biopsy is a non-invasive, real-time method for predicting cancer status and potentially serves as a biomarker source for treatment response. Liquid biopsy includes rich biologically relevant components, such as circulating tumor cells, circulating tumor DNA, and extracellular vesicles (EVs). EVs are particularly intriguing due to their relatively high abundance in most biofluids, with the potential to identify specific cargo derived from circulating tumor EVs. Moreover, normal cells in lymph nodes can uptake EVs, fostering a pre-metastatic microenvironment that facilitates lymph node metastases- a common occurrence in oral cancers. This review encompasses English language publications over the last twenty years, focusing on methods for isolating EVs from saliva, blood, and lymphatic fluids, as well as the collection methods employed. Seventeen cases met the inclusion criteria according to ISEV guidelines, including 10 saliva cases, 6 blood cases, and 1 lymphatic fluid case. This review also highlighted research gaps in oral squamous cell carcinoma (OSCC) EVs, including a lack of multi-omics studies and the exploration of potential EV markers for drug resistance, as well as a notable underutilization of microfluidic technologies to translate liquid biopsy EV findings into clinical applications.
引用
收藏
页码:739 / 759
页数:21
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