Polyether ionophores-promising bioactive molecules for cancer therapy

被引:118
作者
Huczynski, Adam [1 ]
机构
[1] Adam Mickiewicz Univ, Fac Chem, Dept Biochem, PL-60780 Poznan, Poland
关键词
Anticancer properties; Multidrug resistance; Cancer stem cells; Synergistic effect; Chemotherapy; MEDIATED GROWTH-INHIBITION; CELL-CYCLE ARREST; IONIZATION MASS-SPECTROMETRY; MONENSIN-A; X-RAY; MULTIDRUG-RESISTANCE; STEM-CELLS; FT-IR; BIOLOGICAL APPLICATIONS; ANTIBACTERIAL ACTIVITY;
D O I
10.1016/j.bmcl.2012.09.046
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The natural polyether ionophore antibiotics might be important chemotherapeutic agents for the treatment of cancer. In this article, the pharmacology and anticancer activity of the polyether ionophores undergoing pre-clinical evaluation are reviewed. Most of polyether ionophores have shown potent activity against the proliferation of various cancer cells, including those that display multidrug resistance (MDR) and cancer stem cells (CSC). The mechanism underlying the anticancer activity of ionophore agents can be related to their ability to form complexes with metal cations and transport them across cellular and subcellular membranes. Increasing evidence shows that the anticancer activity of polyether ionophores may be a consequence of the induction of apoptosis leading to apoptotic cell death, arresting cell cycle progression, induction of the cell oxidative stress, loss of mitochondrial membrane potential, reversion of MDR, synergistic anticancer effect with other anticancer drugs, etc. Continued investigation of the mechanisms of action and development of new polyether ionophores and their derivatives may provide more effective therapeutic drugs for cancer treatments. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7002 / 7010
页数:9
相关论文
共 105 条
[21]   Characterization of the potent in vitro and in vivo antimalarial activities of ionophore compounds [J].
Gumila, C ;
Ancelin, ML ;
Delort, AM ;
Jeminet, G ;
Vial, HJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (03) :523-529
[22]   Identification of Selective Inhibitors of Cancer Stem Cells by High-Throughput Screening [J].
Gupta, Piyush B. ;
Onder, Tamer T. ;
Jiang, Guozhi ;
Tao, Kai ;
Kuperwasser, Charlotte ;
Weinberg, Robert A. ;
Lander, Eric S. .
CELL, 2009, 138 (04) :645-659
[23]  
HILGENFELD R, 1982, TOP CURR CHEM, V101, P1
[24]  
Huczynski A., 2012, BIOORG MED IN PRESS
[25]  
Huczynski A., J MOL STRUC IN PRESS
[26]   Structures of complexes of benzyl and allyl esters of monensin A with Mg2+, Ca2+, Sr2+, Ba2+ cations studied by ESI-MS and PM5 methods [J].
Huczynski, Adam ;
Brzezinski, Bogumil ;
Bartl, Franz .
JOURNAL OF MOLECULAR STRUCTURE, 2008, 886 (1-3) :9-16
[27]   Synthesis and antimicrobial properties of Monensin A esters [J].
Huczynski, Adam ;
Stefanska, Joanna ;
Przybylski, Piotr ;
Brzezinski, Bogumil ;
Bartl, Franz .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (08) :2585-2589
[28]   Investigation of complex structures of a new 2-hydroxyethyl ester of Monensin A with Mg2+, Ca2+, Sr2+, Ba2+ cations using electrospray ionization mass spectrometry and semiempirical PM5 methods [J].
Huczynski, Adam ;
Przybylski, Piotr ;
Schroeder, Grzegorz ;
Brzezinski, Bogumil .
JOURNAL OF MOLECULAR STRUCTURE, 2007, 829 (1-3) :111-119
[29]   Spectroscopic, mass spectrometry, and semiempirical investigation of a new ester of Monensin A with ethylene glycol and its complexes with monovalent metal cations [J].
Huczynski, Adam ;
Przybylski, Piotr ;
Brzezinski, Bogumil ;
Bartl, Franz .
BIOPOLYMERS, 2006, 82 (05) :491-503
[30]   Spectroscopic and semiempirical studies of a proton channel formed by the methyl ester of monensin A [J].
Huczynski, Adam ;
Przybylski, Piotr ;
Brzezinski, Bogumil ;
Bartl, Franz .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (31) :15615-15623