Abstract
Comparing normal human urothelial (NHU) cells to a panel of six representative urothelial cell carcinoma (UCC)-derived cell lines, we showed that while TRAIL receptor expression patterns were similar, susceptibility to soluble recombinant crosslinked TRAIL fell into three categories. 4/6 carcinoma lines were sensitive, undergoing rapid and extensive death; NHU and 253J cells were partially resistant and HT1376 cells, like normal fibroblasts, were refractory. Both normal and malignant urothelial cells underwent apoptosis via the same caspase-8/9-mediated mechanism. Rapid receptor down-regulation was a mechanism for evasion by some UCC cells. TRAIL resistance in malignant urothelial cells was partially dependent on FLIPL and was differentially mediated by p38(MAPK), whereas in normal cells, resistance was mediated by NF-kappa B. Importantly, extensive killing of UCC cells could be induced using noncrosslinked TRAIL after prolonged exposure, with no damage to their homologous, normal urothelial cell counterparts.
| Original language | English |
|---|---|
| Pages (from-to) | 1564-1576 |
| Number of pages | 13 |
| Journal | Cell death and differentiation |
| Volume | 13 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - Sept 2006 |
Keywords
- apoptosis
- TRAIL
- bladder cancer
- urothelium
- human
- TUMOR-NECROSIS-FACTOR
- APOPTOSIS-INDUCING LIGAND
- NF-KAPPA-B
- BLADDER-CANCER CELLS
- MEDIATED APOPTOSIS
- DECOY RECEPTORS
- CARCINOMA CELLS
- CASPASE-8 ACTIVATION
- SIGNALING COMPLEX
- EPITHELIAL-CELLS