A Synthetic Pan-Aurora Kinase Inhibitor, 5-Methoxy-2-(2-methoxynaphthalen-1-yl)-4H-chromen-4-one, Triggers Reactive Oxygen Species-Mediated Apoptosis in HCT116 Colon Cancer Cells

被引:2
|
作者
Lee, Jeong Yeon [1 ]
Ahn, Sung Shin [1 ]
Jeong, You Jeong [1 ]
Choi, Jihye [1 ]
Ahn, Seunghyun [2 ]
Koh, Dongsoo [2 ]
Lee, Young Han [1 ,3 ]
Lim, Yoongho [3 ,4 ]
Shin, Soon Young [1 ,3 ]
机构
[1] Konkuk Univ, Sanghuh Coll Life Sci, Dept Biol Sci, Seoul 05029, South Korea
[2] Dongduk Womens Univ, Dept Appl Chem, Seoul 02748, South Korea
[3] Konkuk Univ, Canc & Metab Inst, Seoul 05029, South Korea
[4] Konkuk Univ, BMIC, Div Biosci & Biotechnol, Seoul 05029, South Korea
基金
新加坡国家研究基金会;
关键词
UNFOLDED PROTEIN RESPONSE; STRESS-INDUCED APOPTOSIS; TUMOR-SUPPRESSOR P53; ENDOPLASMIC-RETICULUM; OXIDATIVE STRESS; ANTICANCER; MECHANISM; ROLES; PHOSPHORYLATION; EXPRESSION;
D O I
10.1155/2020/3025281
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Aurora kinases are Ser/Thr kinases that function as mitotic regulators. 5-Methoxy-2-(2-methoxynaphthalen-1-yl)-4H-chromen-4-one (DK1913) is a synthetic pan-Aurora kinase inhibitor. However, the mode of action of DK1913 concerning the induction of apoptosis is unclear. Here, we report that DK1913 triggered apoptosis, as revealed by flow cytometry and Annexin V staining. DK1913 enhanced the intracellular levels of reactive oxygen species (ROS) and stimulated the endoplasmic reticulum (ER) and genotoxic stress responses. We also found that DK1913 induced the loss of mitochondrial membrane potential, leading to the activation of caspase-9, caspase-7, and caspase-3. In addition, the antioxidant, butylated hydroxyanisole (BHA), abrogated DK1913-induced loss of mitochondrial membrane potential and activation of the caspase cascade. These findings demonstrate that pan-Aurora kinase inhibitor DK1913 triggers apoptosis through ROS-mediated ER and genotoxic stress responses.
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收藏
页数:11
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