Table 1.
Merits and drawbacks in three different methods for CTCs expansion
| Method | CDX | Short term | Long term |
|---|---|---|---|
| CTC number | High | Low | High |
| Patient origin | Advanced stage only | Early and advanced stage | Advanced stage only |
| Condition | Experimental animal | 10% FCS medium | Defined serum-free medium |
| Sample origin | Organ-vasculature circulation | Peripheral venous or arterial circulation | Peripheral venous or arterial circulation |
| Character | Tumorigenic capacity evaluation; complex procedure and individual difference | Differentiation and limited proliferation ability with significant phenotypic alterations | Phenotype stable; maintaining the tumorigenicity in non-adherent status |
| Research purpose | Simulate microenvironment in vivo | Expand enough CTCs for downstream analyses | Enrich and expand CTCs to establish patient-derived cell lines for long-term research |
| Cost | High | Cheap | Moderate |
| Culture cycle | Several months | 1-2 weeks | Several months −1 year |
| Successful rate | Low | Moderate | Low |