Sulfiredoxin inhibitor induces preferential death of cancer cells through reactive oxygen species-mediated mitochondrial damage

• Published in: Free radical biology & medicine Vol. 91; pp. 264 - 274
• Main Authors: Kim, Hojin, Lee, Gong-Rak, Kim, Jiwon, Baek, Jin Young, Jo, You-Jin, Hong, Seong-Eun, Kim, Sung Hoon, Lee, Jiae, Lee, Hye In, Park, Song-Kyu, Kim, Hwan Mook, Lee, Hwa Jeong, Chang, Tong-Shin, Rhee, Sue Goo, Lee, Ju-Seog, Jeong, Woojin
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.02.2016
• Subjects: Animals; Antineoplastic Agents - pharmacology; Apoptosis; Apoptosis - drug effects; Benzoates - pharmacology; Cancer; Cell Line, Tumor; Female; Humans; Mice, Inbred BALB C; Mice, Nude; Mitochondria - drug effects; Mitochondrial damage; Oxidation-Reduction; Oxidative Stress - drug effects; Oxidoreductases Acting on Sulfur Group Donors - antagonists & inhibitors; Reactive oxygen species; Reactive Oxygen Species - metabolism; Sulfiredoxin; Tumor Burden - drug effects; Xenograft Model Antitumor Assays; PBS; Reactive oxygen species; DMSO; PO-1; H2O2; NAC; SD; FITC; ΔΨm; ROS; Mitochondrial damage; Srx; PI; BHA; MPTP; Prxs; Trx; Sulfiredoxin; NAO; Cancer; Apoptosis
• ISSN: 0891-5849; 1873-4596
• DOI: 10.1016/j.freeradbiomed.2015.12.023

Recent studies have shown that many types of cancer cells have increased levels of reactive oxygen species (ROS) and enhance antioxidant capacity as an adaptation to intrinsic oxidative stress, suggesting that cancer cells are more vulnerable to oxidative insults and are more dependent on antioxidant systems compared with normal cells. Thus, disruption of redox homeostasis caused by a decline in antioxidant capacity may provide a method for the selective death of cancer cells. Here we show that ROS-mediated selective death of tumor cells can be caused by inhibiting sulfiredoxin (Srx), which reduces hyperoxidized peroxiredoxins, leading to their reactivation. Srx inhibitor increased the accumulation of sulfinic peroxiredoxins and ROS, which led to oxidative mitochondrial damage and caspase activation, resulting in the death of A549 human lung adenocarcinoma cells. Srx depletion also inhibited the growth of A549 cells like Srx inhibition, and the cytotoxic effects of Srx inhibitor were considerably reversed by Srx overexpression or antioxidants such as N-acetyl cysteine and butylated hydroxyanisol. Moreover, Srx inhibitor rendered tumorigenic ovarian cells more susceptible to ROS-mediated death compared with nontumorigenic cells and significantly suppressed the growth of A549 xenografts without acute toxicity. Our results suggest that Srx might serve as a novel therapeutic target for cancer treatment based on ROS-mediated cell death. [Display omitted] •Srx inhibitor induces the accumulation of sulfinic peroxiredoxins and ROS.•Srx inhibitor causes the death of cancer cells by oxidative mitochondrial damage.•Srx inhibitor leads to preferential death of cancer cells over normal cells.•Srx inhibitor suppresses the growth of xenograft tumors without acute toxicity.•Targeting Srx might be a novel therapeutic strategy for cancer treatment.