Table 3.
Cytotoxic effects of enoxacin depending on the concentration in various cancer cell lines and animal tissues.
| Effect | Conc. [μM] | Cell Line/Tissue | Ref. |
|---|---|---|---|
| No cytotoxicity | 31 | A673 | [74] |
| 124 | Wi-38, MRC-5 | [36] | |
| 20 | HEK 293 | [91] | |
| 5–100 | Primary BMMs | [82] | |
| 5–100 | Raw 264.7 | [77] | |
| No genotoxicity | 0–3121 | WTK-1 | [90] |
| Apoptosis | 62 | NCI-H460 | [70] |
| 150 | H460, A549 | [69] | |
| Apoptosis, cell cycle arrest | 31–156 | MCF-7 | [71] |
| 20–80 | HeLa, C33A | [73] | |
| 124 | DU145, LNCaP, VCaP, PC-3, 22Rv1, Co115 | [38] | |
| 124 | HCT-116, RKO | [36] | |
| Cytotoxicity (PI) | 78–312 | A375 | [48] |
| Cytotoxicity (MTS) | 31 | TC 252, Patient derived ESFT spheres | [74] |
| Cytotoxicity (MTT) | 124 | HCT-116, RKO, HepG2, SNU-1, SNU-638, MDA-MB 231, MCF-7, H23, H1299, A549, MDA-MB-231, HepG2, KG1a, RAJI | [36] |
| 124 | A673, TC252, STA-ET-8.2 | [37] | |
| 156 | A375, Mel-Juso, Mel-Ho | [48] | |
| 12.5–100 | A549 | [45] | |
| Decreased invasiveness | 124 | DU145 | [38] |
| Cytochrome P450 inhibition | 10–1000 | freshly isolated rat hepatocytes | [75] |
| Inhibition of osteoclastogenesis | 10; 100 | Primary MMO | [76] |
| 10–100 | Primary MMO, Raw 264.7 | [77] | |
| 5; 10; 50 | Primary BMMs | [82] | |
| Inhibition of bone resorption | 10; 25; 100 | Primary MMO | [76] |
| 5; 10; 50 | Primary BMMs | [82] | |
| Inhibition of the interaction between V-ATPase B-subunit and F-actin | 10; 25; 100 | rabbit muscle actin and the Vma2p-MBP microfilaments | [76] |
| Inhibition of the interaction between microfilaments and V-ATPase (a) B2-subunit (b) a3-subunit | 50 | Primary MMO | [77] |
| Impairment of JNK signaling | 25 | Raw 264.7 | [82] |
Abbreviations: propidium iodide (PI); Ewing sarcoma family tumor (ESFT); mouse marrow osteoclasts (MMO); bone-marrow-derived macrophages (BMMs); maltose-binding protein (MBP); vacuolar H+-ATPase (V-ATPase).