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
[1]   Carboxylic ionophores in malaria chemotherapy: The effects of monensin and nigericin on Plasmodium falciparum in vitro and Plasmodium vinckei petteri in vivo [J].
Adovelande, J ;
Schrevel, J .
LIFE SCIENCES, 1996, 59 (20) :PL309-PL315
[2]   Cancer stem cells in solid tumors [J].
Ailles, Laurie E. ;
Weissman, Irving L. .
CURRENT OPINION IN BIOTECHNOLOGY, 2007, 18 (05) :460-466
[3]   Cytostatic effect of inostamycin, an inhibitor of cytidine 5′-diphosphate 1,2-diacyl-sn-glycerol (CDP-DG):: Inositol transferase, on oral squamous cell carcinoma cell lines [J].
Baba, Y ;
Tsukuda, M ;
Mochimatsu, I ;
Furukawa, S ;
Kagata, H ;
Nagashima, Y ;
Koshika, S ;
Imoto, M ;
Kato, Y .
CELL BIOLOGY INTERNATIONAL, 2001, 25 (07) :613-620
[4]   Inostamycin prevents malignant phenotype of cancer: inhibition of phosphatidylinositol synthesis provides a therapeutic advantage for head and neck squamous cell carcinoma [J].
Baba, Yuh ;
Kato, Yasumasa ;
Ogawa, Kaoru .
CELL BIOLOGY INTERNATIONAL, 2010, 34 (02) :171-175
[5]   The role of natural product chemistry in drug discovery [J].
Butler, MS .
JOURNAL OF NATURAL PRODUCTS, 2004, 67 (12) :2141-2153
[6]   Forty years of monensin for the control of coccidiosis in poultry [J].
Chapman, H. D. ;
Jeffers, T. K. ;
Williams, R. B. .
POULTRY SCIENCE, 2010, 89 (09) :1788-1801
[7]   The Warburg effect and its cancer therapeutic implications [J].
Chen, Zhao ;
Lu, Weiqin ;
Garcia-Prieto, Celia ;
Huang, Peng .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 2007, 39 (03) :267-274
[8]   Lessons from natural molecules [J].
Clardy, J ;
Walsh, C .
NATURE, 2004, 432 (7019) :829-837
[9]  
COLOMBATTI M, 1990, CANCER RES, V50, P1385
[10]  
Deguchi A, 1996, J BIOCHEM-TOKYO, V120, P1118