source |
Blood, urine, saliva, synovial fluid, cerebrospinal fluid, etc. |
Blood, cerebrospinal fluid, urine, etc. |
Blood, urine, cerebrospinal fluid, ascites, pleural fluid, etc. |
scale |
Nanoscale (DNA fragments) |
cellular level |
Nanoscale (40–150 nm) |
information load |
Can carry information on multiple genetic variants |
Complete genetic information, including genome, transcriptome, epigenetic variation |
Carrying proteins, RNA and many other biomolecules |
clinical significance |
Early screening, companion diagnosis, prognostic assessment, MRD testing |
Prognostic assessment, drug sensitivity prediction, drug resistance mechanism studies |
Early diagnosis, prognostic assessment, drug response monitoring |
stability |
Relatively low (short half-life) |
high |
High (phospholipid bilayer protection) |
rarity |
High (especially in early-stage tumors) |
high |
moderate (interference from other vesicles in body fluids) |
heterogeneity |
low |
High (large variation between CTCs) |
moderate |
Difficulty of isolation and purification |
moderate |
High (not yet standardized) |
High (technically complex) |
background noise |
Moderate (normal cfDNA interference) |
low |
Moderate (interference from other vesicles in body fluids) |
Difficulty of standardization |
moderate |
high |
high |
technical difficulty |
Moderate (relies on high-sensitivity detection technology) |
High (complex enrichment, identification techniques) |
Medium (dependent on specific detection techniques) |
operating difficulty |
low |
High (multi-step operation) |
moderate |