Cracking the Cytotoxicity Code: Apoptotic Induction of 10-Acetylirciformonin B is Mediated through ROS Generation and Mitochondrial Dysfunction

Marine Drugs

Huei-Chuan Shih⁷  Mohamed El-Shazly¹  Yung-Shun Juan⁵  Chao-Yuan Chang³  Jui-Hsin Su⁴  Yu-Cheng Chen⁴  Shou-Ping Shih⁴  Huei-Mei Chen²  Yang-Chang Wu⁶ 

[1] Department of Pharmacognosy and Natural Products Chemistry, Faculty of Pharmacy, Ain-Shams University, Organization of African Unity Street, Abassia, Cairo 11566, Egypt; E-Mail:;Pingtung Branch of Kaohsiung Veterans General Hospital, Nutrition Branch, Pingtung 912, Taiwan; E-Mail:;Department of Anatomy, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan; E-Mail:;Graduate Institute of Marine Biotechnology, National Dong Hwa University, Pingtung 944, Taiwan; E-Mails:;Department of Urology, Kaohsiung Municipal Hsiao-Kang Hospital, Kaohsiung 812, Taiwan; E-Mail:;Natural Medicinal Products Research Center, China Medical University Hospital, Taichung 404, Taiwan;Department of Nursing, Meiho University, Pingtung 912, Taiwan; E-Mail:

关键词: 10-acetylirciformonin B;    apoptosis;    hexokinase;    mitochondria;    reactive oxygen species (ROS);    topoisomerase;   

DOI  :  10.3390/md12053072

来源: mdpi

【 摘 要 】

A marine furanoterpenoid derivative, 10-acetylirciformonin B (10AB), was found to inhibit the proliferation of leukemia, hepatoma, and colon cancer cell lines, with selective and significant potency against leukemia cells. It induced DNA damage and apoptosis in leukemia HL 60 cells. To fully understand the mechanism behind the 10AB apoptotic induction against HL 60 cells, we extended our previous findings and further explored the precise molecular targets of 10AB. We found that the use of 10AB increased apoptosis by 8.9%–87.6% and caused disruption of mitochondrial membrane potential (MMP) by 15.2%–95.2% in a dose-dependent manner, as demonstrated by annexin-V/PI and JC-1 staining assays, respectively. Moreover, our findings indicated that the pretreatment of HL 60 cells with N-acetyl-l-cysteine (NAC), a reactive oxygen species (ROS) scavenger, diminished MMP disruption and apoptosis induced by 10AB, suggesting that ROS overproduction plays a crucial rule in the cytotoxic activity of 10AB. The results of a cell-free system assay indicated that 10AB could act as a topoisomerase catalytic inhibitor through the inhibition of topoisomerase IIα. On the protein level, the expression of the anti-apoptotic proteins Bcl-xL and Bcl-2, caspase inhibitors XIAP and survivin, as well as hexokinase II were inhibited by the use of 10AB. On the other hand, the expression of the pro-apoptotic protein Bax was increased after 10AB treatment. Taken together, our results suggest that 10AB-induced apoptosis is mediated through the overproduction of ROS and the disruption of mitochondrial metabolism.

【 授权许可】

CC BY   
© 2014 by the authors; licensee MDPI, Basel, Switzerland.