Table 1.
Relative proliferation rate of bladder cancer cell lines treated with PPARG modulators.
| Cell Line | Pathway Alteration | GW9662 | SR2595 | T0070907 | SR10221 |
|---|---|---|---|---|---|
| HT-1197 | RXRA p.S427F | 127 | 78 | 48** | 64* |
| 5637 | PPARG amplified | 93 | 117 | 51** | 73** |
| UM-UC-9 | PPARG amplified | 108 | 97 | 19** | 20** |
| RT112/84 | PPARG signature | 98 | 101 | 69** | 80** |
| UM-UC-1 | PPARG signature | 96 | 84 | 47** | 62** |
| Cal29 | PPARG signature | 97 | 86 | 55** | 74* |
| SW1710 | Not altered | 99 | 91 | 96 | 81 |
| KU19.19 | Not altered | 85 | 91 | 95 | 91 |
| UM-UC-3 | Not altered | 92 | 102 | 91 | 96 |
Relative proliferation rate of bladder cancer cell lines treated with PPARG inhibitors at 100nM compared to DMSO vehicle, reported as percent of vehicle control (POC), in long-term kinetic proliferation assays. Percent of DMSO control was calculated by determining the relative number of cells for treatment versus DMSO control at the timepoint where DMSO control reached 50% confluence (see Fig. 4B for graphical representation) by counting fluorescently labeled nuclei (IncuCyte Zoom). Significant differences in cell number for test sample relative to DMSO control were calculated using two-way ANOVA with Dunnett’s multiple comparison test(*P<0.01, **P <0.001).