Calyculin A causes sensitization to tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced apoptosis by ROS-mediated down-regulation of cellular FLICE-inhibiting protein (c-FLIP) and by enhancing death receptor 4 mRNA stabilization
- Affiliated Author(s)
- 권택규
- Alternative Author(s)
- Kwon, Taeg Kyu
- Journal Title
- Apoptosis
- ISSN
- 1360-8185
- Issued Date
- 2012
- Abstract
- Calyculin A (Cal A) is a serine/threonine
phosphatase inhibitor that is capable of inducing apoptosis
in cancer cells. In this study, we examined whether Cal A
could modulate TRAIL-induced apoptosis in human renal
carcinoma-derived Caki cells. Our results show that Cal A
is capable of sensitizing Caki cells to TRAIL-induced
apoptosis, as well as U2OS human osteosarcoma cells and
A549 human lung adenocarcinoma epithelial cells. Cal A
increases intracellular ROS production and down-regulates
c-FLIP(L) expression. Interestingly, the down-regulation of
protein phosphatase 1 (PP1) by PP1 siRNA also reduced
c-FLIP(L) expression via reactive oxygen species production.
Furthermore, Cal A induced death receptor 4 (DR4)
mRNA and protein expression by enhancing DR4 mRNA
stability. We also found that PP4 siRNA up-regulated DR4
mRNA and protein expression. Collectively, our results
suggest that Cal A could enhance TRAIL-mediated apoptosis
via the down-regulation of c-FLIP(L) and the
up-regulation of DR4 in human renal cell carcinoma cell
line Caki.
Keywords Calyculin A TRAIL Death receptor
c-FLIP(L) Reactive oxygen species Protein phosphatase
- Authorize & License
-
- AuthorizeOpen
- EmbargoForever
- Files in This Item:
-
Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.