An Ethacrynic Acid-Brominated BODIPY Photosensitizer (EA-BPS) Construct Enhances the Lethality of Reactive Oxygen Species in Hypoxic Tumor-Targeted Photodynamic Therapy

被引:91
作者
Won, Miae [1 ]
Koo, Seyoung [1 ]
Li, Hao [2 ]
Sessler, Jonathan L. [3 ]
Lee, Jin Yong [2 ]
Sharma, Amit [4 ]
Kim, Jong Seung [1 ]
机构
[1] Korea Univ, Dept Chem, Seoul 02841, South Korea
[2] Sungkyunkwan Univ, Dept Chem, Suwon 16419, South Korea
[3] Univ Texas Austin, Dept Chem, Austin, TX 78712 USA
[4] CSIR Cent Sci Instruments Org, Sect 30 C, Chandigarh 160030, India
基金
新加坡国家研究基金会;
关键词
BODIPY; ethacrynic acid; glutathione S-transferase-pi; Hypoxia; photodynamic therapy; S-GLUTATHIONYLATION; SIGNALING PATHWAYS; ADJUVANT THERAPY; CANCER; CELLS; RESISTANCE; CHEMILUMINESCENCE; BIOLUMINESCENCE; PROLIFERATION; SENSITIVITY;
D O I
10.1002/anie.202012687
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite being a clinically approved intervention for cancer, photodynamic therapy (PDT) still suffers from limitations. Prime among these is a therapeutic response that is mostly oxygen dependent. This limits the utility of PDT in treating hypoxic tumors since lower levels of cytotoxic reactive oxygen species (ROS) are generated in regions of low oxygen tension. Glutathione-pi (GST-pi) is a key enzyme that militates against ROS-mediated apoptosis. We report herein a new construct, EA-BPS, that contains both a brominated BODIPY photosensitizer (BPS) and an ethacrynic acid (EA) GST-pi inhibitor. Photoirradiation of EA-BPS induces a synergistic antitumor effect that results from the combination of ROS production and GST-pi inhibition. Relative to BPS alone, an enhanced cell-killing effect is seen under hypoxic conditions both in vitro and in vivo. We conclude that by making better use of the available oxygen in tumor environments, improved therapeutic PDT outcomes should be achievable even under hypoxic conditions.
引用
收藏
页码:3196 / 3204
页数:9
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