Table 1. Summary of drugs screened in senescent AEC model, their respective IC50s per endpoint, and their fold selectivity for senescent versus non-senescent AECs.
Drug | Mechanism | Class | IC50 (μM) | Senescence Selectivity (fold) | |||||||
CellTiter-Glo | IL-6 | IL-8 | |||||||||
Non-senescent AECs | Senescent AECs | Non-senescent AECs | Senescent AECs | Non-senescent AECs | Senescent AECs | CellTiter-Glo | IL-6 | IL-8 | |||
Nintedanib | TGF-β signaling | Anti-fibrotic (SoC) | 48.1 ± 3.0 | 24.1 ± 19.2 | 50 | 38.2 ± 14.3 | 34.2 ± 16.9 | 37.9 ± 14.4 | 2.0 | 1.3 | 0.9 |
ABT-317 | Jak1 | Senomorphic | 10 | 10 | 10 | 10 | 10 | 10 | 1.0 | 1.0 | 1.0 |
Ruxolitinib | Jak1/2 | Senomorphic | 10 | 10 | 10 | 10 | 10 | 10 | 1.0 | 1.0 | 1.0 |
Navitoclax | Bcl-2/xL | Senolytic | 2.6 ± 3.8 | 0.06 ± 0.03 | 9.4 ± 0.55 | 0.13 ± 0.03 | 10 | 0.07 ± 0.02 | 44.6 | 71.0 | 134.2 |
AD80 | RET, Raf, SRC, S6K | Senomorphic and weak senolytic | 2.3 ± 0.5 | 0.46 ± 0.75 | 0.5 ± 0.1 | 0.42 ± 0.13 | 0.73 ± 0.13 | 0.37 ± 0.03 | 5.1 | 1.2 | 1.9 |
Values represent the geometric mean ± SEM of 3-4 experimental repeats.