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
相关论文
共 46 条
[31]   A novel pathway for the production of hydrogen sulfide from D-cysteine in mammalian cells [J].
Shibuya, Norihiro ;
Koike, Shin ;
Tanaka, Makiko ;
Ishigami-Yuasa, Mari ;
Kimura, Yuka ;
Ogasawara, Yuki ;
Fukui, Kiyoshi ;
Nagahara, Noriyuki ;
Kimura, Hideo .
NATURE COMMUNICATIONS, 2013, 4
[32]   A DIRECT MICRODETERMINATION FOR SULFIDE [J].
SIEGEL, LM .
ANALYTICAL BIOCHEMISTRY, 1965, 11 (01) :126-&
[33]   Hydrogen sulphide and its therapeutic potential [J].
Szabo, Csaba .
NATURE REVIEWS DRUG DISCOVERY, 2007, 6 (11) :917-935
[34]   Tumor-derived hydrogen sulfide, produced by cystathionine-β-synthase, stimulates bioenergetics, cell proliferation, and angiogenesis in colon cancer [J].
Szabo, Csaba ;
Coletta, Ciro ;
Chao, Celia ;
Modis, Katalin ;
Szczesny, Bartosz ;
Papapetropoulos, Andreas ;
Hellmich, Mark R. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (30) :12474-12479
[35]   AP39, a novel mitochondria-targeted hydrogen sulfide donor, stimulates cellular bioenergetics, exerts cytoprotective effects and protects against the loss of mitochondrial DNA integrity in oxidatively stressed endothelial cells in vitro [J].
Szczesny, Bartosz ;
Modis, Katalin ;
Yanagi, Kazunori ;
Coletta, Ciro ;
Le Trionnaire, Sophie ;
Perry, Alexis ;
Wood, Mark E. ;
Whiteman, Matthew ;
Szabo, Csaba .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2014, 41 :120-130
[36]   QUANTITATIVE STUDIES OF GROWTH OF MOUSE EMBRYO CELLS IN CULTURE AND THEIR DEVELOPMENT INTO ESTABLISHED LINES [J].
TODARO, GJ ;
GREEN, H .
JOURNAL OF CELL BIOLOGY, 1963, 17 (02) :299-&
[37]   Hydrogen sulfide-releasing anti-inflammatory drugs [J].
Wallace, John L. .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2007, 28 (10) :501-505
[38]   DEMONSTRATION THAT MUTATION OF THE TYPE-II TRANSFORMING GROWTH-FACTOR-BETA RECEPTOR INACTIVATES ITS TUMOR-SUPPRESSOR ACTIVITY IN REPLICATION ERROR-POSITIVE COLON-CARCINOMA CELLS [J].
WANG, J ;
SUN, LZ ;
MYEROFF, L ;
WANG, XF ;
GENTRY, LE ;
YAN, JH ;
LIANG, JR ;
ZBOROWSKA, E ;
MARKOWITZ, S ;
WILLSON, JKV ;
BRATTAIN, MG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (37) :22044-22049
[39]   Two's company, three's a crowd:: can H2S be the third endogenous gaseous transmitter? [J].
Wang, R .
FASEB JOURNAL, 2002, 16 (13) :1792-1798
[40]   PHYSIOLOGICAL IMPLICATIONS OF HYDROGEN SULFIDE: A WHIFF EXPLORATION THAT BLOSSOMED [J].
Wang, Rui .
PHYSIOLOGICAL REVIEWS, 2012, 92 (02) :791-896