Wang, F., Chen, H., Yan, X. et al. Fascaplysin sensitizes cells to TRAIL-induced apoptosis through upregulating DR5 expression., Chin. J. Ocean. Limnol. 31, 560–569 (2013). https://doi.org/10.1007/s00343-013-2215-y
DOI:
Wang, F., Chen, H., Yan, X. et al. Fascaplysin sensitizes cells to TRAIL-induced apoptosis through upregulating DR5 expression., Chin. J. Ocean. Limnol. 31, 560–569 (2013). https://doi.org/10.1007/s00343-013-2215-yDOI:
Fascaplysin sensitizes cells to TRAIL-induced apoptosis through upregulating DR5 expression
摘要
Abstract
This study investigated the molecular mechanism of anti-tumor effect of fascaplysin
a nitrogenous red pigment firstly isolated from a marine sponge. Microarray analysis show that the TNF and TNF receptor superfamily in human umbilical vein endothelial cells (HUVEC) and human hepatocarcinoma cells (BEL-7402) were significantly regulated by fascaplysin. Western Blot results reveal that fascaplysin increased the expression of cleaved caspase-9
active caspase-3
and decreased the level of procaspase-8 and Bid. Flow cytometry and cytotoxicity tests indicate that fascaplysin sensitized cells to tumor necrosis-related apoptosisinducing ligand-(TRAIL) induced apoptosis
which was markedly blocked by TRAIL R2/Fc chimera
a dominant negative form of TRAIL receptor DR5. Therefore
our results demonstrate that fascaplysin promotes apoptosis through the activation of TRAIL signaling pathway by upregulating DR5 expression.
关键词
Keywords
references
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