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
- Author(s)
- Seon Min Woo; Kyoung-jin Min; Taeg Kyu Kwon
- Keimyung Author(s)
- Kwon, Taeg Kyu
- Department
- Dept. of Immunology (면역학)
- Journal Title
- Apoptosis
- Issued Date
- 2012
- Volume
- 17
- Issue
- 11
- 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
- Keimyung Author(s)(Kor)
- 권택규
- Publisher
- School of Medicine
- Citation
- Seon Min Woo et al. (2012). 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. Apoptosis, 17(11), 1223–1234. doi: 10.1007/s10495-012-0753-y
- Type
- Article
- ISSN
- 1360-8185
- Source
- https://link.springer.com/article/10.1007%2Fs10495-012-0753-y
- DOI
- 10.1007/s10495-012-0753-y
- URI
- https://kumel.medlib.dsmc.or.kr/handle/2015.oak/35070
-
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