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

Author:

Lee Jeong Yeon1ORCID,Ahn Sung Shin1ORCID,Jeong You Jeong1ORCID,Choi Jihye1ORCID,Ahn Seunghyun2ORCID,Koh Dongsoo2ORCID,Lee Young Han13ORCID,Lim Yoongho34ORCID,Shin Soon Young13ORCID

Affiliation:

1. Department of Biological Sciences, Sanghuh College of Life Sciences, Konkuk University, Seoul 05029, Republic of Korea

2. Department of Applied Chemistry, Dongduk Women’s University, Seoul 02748, Republic of Korea

3. Cancer and Metabolism Institute, Konkuk University, Seoul 05029, Republic of Korea

4. Division of Bioscience and Biotechnology, BMIC, Konkuk University, Seoul 05029, Republic of Korea

Abstract

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.

Funder

Konkuk University

Publisher

Hindawi Limited

Subject

General Chemistry

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