H2S-Releasing Polymer Micelles for Studying Selective Cell Toxicity

被引:79
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
    Shibuya, Norihiro
    Koike, Shin
    Tanaka, Makiko
    Ishigami-Yuasa, Mari
    Kimura, Yuka
    Ogasawara, Yuki
    Fukui, Kiyoshi
    Nagahara, Noriyuki
    Kimura, Hideo
    [J]. NATURE COMMUNICATIONS, 2013, 4
  • [32] A DIRECT MICRODETERMINATION FOR SULFIDE
    SIEGEL, LM
    [J]. ANALYTICAL BIOCHEMISTRY, 1965, 11 (01) : 126 - &
  • [33] Hydrogen sulphide and its therapeutic potential
    Szabo, Csaba
    [J]. 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
    Szabo, Csaba
    Coletta, Ciro
    Chao, Celia
    Modis, Katalin
    Szczesny, Bartosz
    Papapetropoulos, Andreas
    Hellmich, Mark R.
    [J]. 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
    Szczesny, Bartosz
    Modis, Katalin
    Yanagi, Kazunori
    Coletta, Ciro
    Le Trionnaire, Sophie
    Perry, Alexis
    Wood, Mark E.
    Whiteman, Matthew
    Szabo, Csaba
    [J]. 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
    TODARO, GJ
    GREEN, H
    [J]. JOURNAL OF CELL BIOLOGY, 1963, 17 (02) : 299 - &
  • [37] Hydrogen sulfide-releasing anti-inflammatory drugs
    Wallace, John L.
    [J]. 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
    WANG, J
    SUN, LZ
    MYEROFF, L
    WANG, XF
    GENTRY, LE
    YAN, JH
    LIANG, JR
    ZBOROWSKA, E
    MARKOWITZ, S
    WILLSON, JKV
    BRATTAIN, MG
    [J]. 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?
    Wang, R
    [J]. FASEB JOURNAL, 2002, 16 (13) : 1792 - 1798
  • [40] PHYSIOLOGICAL IMPLICATIONS OF HYDROGEN SULFIDE: A WHIFF EXPLORATION THAT BLOSSOMED
    Wang, Rui
    [J]. PHYSIOLOGICAL REVIEWS, 2012, 92 (02) : 791 - 896