H2S-Releasing Polymer Micelles for Studying Selective Cell Toxicity

被引:83
作者
Foster, Jeffrey C. [1 ,2 ]
Radzinski, Scott C. [1 ,2 ]
Zou, Xianlin [3 ,4 ]
Finkielstein, Carla V. [3 ,4 ]
Matson, John B. [1 ,2 ]
机构
[1] Virginia Tech, Dept Chem, Macromol Innovat Inst, Blacksburg, VA 24061 USA
[2] Virginia Tech, Ctr Drug Discovery, Blacksburg, VA 24061 USA
[3] Virginia Tech, Dept Biol Sci, Blacksburg, VA 24061 USA
[4] Virginia Tech, Biocomplex Inst, Blacksburg, VA 24061 USA
基金
美国国家科学基金会;
关键词
gasotransmitter; H2S donors; controlled release; polymer amphiphiles; RAFT; HYDROGEN-SULFIDE H2S; FLUORESCENT-PROBES; CANCER-CELLS; COLON-CANCER; GROWTH; RELEASE; TISSUE; NANOPARTICLES; BIOENERGETICS; ANGIOGENESIS;
D O I
10.1021/acs.molpharmaceut.6b01117
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We report the preparation of S-aroylthiooxime (SATO) functionalized amphiphilic block copolymer micelles that release hydrogen sulfide (H2S), a gaseous signaling molecule of relevance to various physiological and pathological conditions. The micelles release 75 H2S in response to cysteine with a half-life of 3.3 h, which is substantially slower than a related small molecule SATO. Exogenous administration of H2S impacts growth and proliferation of cancer cells; however, the limited control over H2S generation from inorganic sulfide sources results in conflicting reports. Therefore, we compare the cellular cytotoxicity of SATO-functionalized micelles, which release H2S in a sustained manner, to Na2S, which releases H2S in a single dose. Our results show that H2S-releasing micelles significantly reduce the survival of HCT116 colon cancer cells relative to Na2S, GYY4137, and a small molecule SATO, indicating that release kinetics may play an important role in determining toxicity of H2S toward cancer cells. Furthermore, H2S-releasing micelles are well tolerated by immortalized fibroblasts (NIH/3T3 cells), suggesting a selective toxicity of H2S toward cancer cells.
引用
收藏
页码:1300 / 1306
页数:7
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