Proscillaridin A Sensitizes Human Colon Cancer Cells to TRAIL-Induced Cell Death

被引:3
作者
Semba, Manami [1 ,2 ]
Takamatsu, Shinji [3 ]
Komazawa-Sakon, Sachiko [1 ]
Miyoshi, Eiji [3 ]
Nishiyama, Chiharu [2 ]
Nakano, Hiroyasu [1 ]
Moriwaki, Kenta [1 ]
机构
[1] Toho Univ, Grad Sch Med, Dept Biochem, Ota Ku, Tokyo 1438540, Japan
[2] Tokyo Univ Sci, Fac Adv Engn, Dept Biol Sci & Technol, Katsushika Ku, Tokyo 1258585, Japan
[3] Osaka Univ, Fac Med, Grad Sch Med, Dept Mol Biochem & Clin Invest, Suita, Osaka 5650871, Japan
关键词
TRAIL; apoptosis; cardiac glycoside; O-glycosylation; INDUCED APOPTOSIS; CARDIAC-GLYCOSIDES; DOWN-REGULATION; UP-REGULATION; LIGAND; GLYCOSYLATION; ACTIVATION; RESISTANCE; INHIBITOR; MCL-1;
D O I
10.3390/ijms23136973
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is a cytotoxic cytokine that induces cancer cell death by binding to TRAIL receptors. Because of its selective cytotoxicity toward cancer cells, TRAIL therapeutics, such as recombinant TRAIL and agonistic antibodies targeting TRAIL receptors, have garnered attention as promising cancer treatment agents. However, many cancer cells acquire resistance to TRAIL-induced cell death. To overcome this issue, we searched for agents to sensitize cancer cells to TRAIL-induced cell death by screening a small-molecule chemical library consisting of diverse compounds. We identified a cardiac glycoside, proscillaridin A, as the most effective TRAIL sensitizer in colon cancer cells. Proscillaridin A synergistically enhanced TRAIL-induced cell death in TRAIL-sensitive and -resistant colon cancer cells. Additionally, proscillaridin A enhanced cell death in cells treated with TRAIL and TRAIL sensitizer, the second mitochondria-derived activator of caspase mimetic. Proscillaridin A upregulated TRAIL receptor expression, while downregulating the levels of the anti-cell death molecules, cellular FADD-like IL-1 beta converting enzyme-like inhibitor protein and Mcl1, in a cell type-dependent manner. Furthermore, proscillaridin A enhanced TRAIL-induced cell death partly via O-glycosylation. Taken together, our findings suggest that proscillaridin A is a promising agent that enhances the anti-cancer efficacy of TRAIL therapeutics.
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页数:15
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