细胞外小泡
液体活检
胞外囊泡
微泡
癌症
生物标志物
癌症生物标志物
医学
生物标志物发现
病理
细胞生物学
生物
生物信息学
小RNA
内科学
蛋白质组学
生物化学
基因
作者
Tony Hu,Joy Wolfram,Sudhir Srivastava
标识
DOI:10.1016/j.trecan.2020.09.003
摘要
Cancer screening has substantially reduced cancer mortality but is limited by low compliance due to expense or resistance to the required procedure and any confirmatory tissue biopsies. Liquid biopsies employing extracellular vesicles can provide a wealth of tumor information and have the potential to replace conventional screening and increase compliance. Current biomarker discovery and validation efforts are limited by challenges associated with isolating and analyzing specific extracellular vesicle populations in lipid biopsies with current methods. Recent methylation and glycome analyses may provide valuable new information to improve tumor diagnosis and evaluate tumor type. New streamlined approaches that provide robust data and large well-designed validation are necessary for the future clinical translation of liquid biopsy-based cancer diagnostics. Early cancer diagnosis is critical for improving patient survival and mortality rates, but most diagnostics on solid tumors rely on imaging tests with limited sensitivity and specificity to identify potential cases, which are then confirmed by tissue biopsies. However, this process is usually not suitable for cancer screening or evaluation of tumor responses to treatment. Liquid biopsies have the potential to bridge this gap, but few such assays have been approved for cancer applications. Extracellular vesicles hold particular promise for liquid biopsy diagnostics but are currently limited by the lack of robust methods for isolation and analysis. New isolation and analysis techniques, however, show promise to improve the clinical utility of extracellular vesicle-based cancer diagnosis. Early cancer diagnosis is critical for improving patient survival and mortality rates, but most diagnostics on solid tumors rely on imaging tests with limited sensitivity and specificity to identify potential cases, which are then confirmed by tissue biopsies. However, this process is usually not suitable for cancer screening or evaluation of tumor responses to treatment. Liquid biopsies have the potential to bridge this gap, but few such assays have been approved for cancer applications. Extracellular vesicles hold particular promise for liquid biopsy diagnostics but are currently limited by the lack of robust methods for isolation and analysis. New isolation and analysis techniques, however, show promise to improve the clinical utility of extracellular vesicle-based cancer diagnosis.
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