Phenazines and cancer

被引:112
作者
Cimmino, Alessio [5 ]
Evidente, A. [5 ]
Mathieu, V. [1 ,2 ]
Andolfi, A. [5 ]
Lefranc, F. [1 ,2 ,3 ]
Kornienko, A. [4 ]
Kiss, R. [1 ,2 ]
机构
[1] Fac Pharm, Toxicol Lab, B-1050 Brussels, Belgium
[2] Univ Libre Bruxelles, B-1050 Brussels, Belgium
[3] Univ Libre Bruxelles, Serv Neurochirurg, Hop Erasme, B-1050 Brussels, Belgium
[4] New Mexico Inst Min & Technol, Dept Chem, Socorro, NM 87801 USA
[5] Univ Naples Federico II, Dipartimento Sci Suolo Pianta Ambiente & Prod Ani, I-80055 Portici, Italy
关键词
POTENTIAL ANTITUMOR AGENTS; IN-VITRO; STREPTOMYCES-ANTIBIOTICUS; CYTOTOXICITY EVALUATION; SYNTHETIC ANALOGS; TOPOISOMERASE-I; PD 116,152; PHASE-I; XR5944; BIOSYNTHESIS;
D O I
10.1039/c2np00079b
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Phenazines are a large group of natural and synthesised nitrogen-containing heterocycles, including more than 100 different compounds of natural origin and over 6000 synthetic compounds. Many of these compounds have been investigated as potential anti-cancer agents. Despite a large number of research publications, no recent attempt to summarise and critically evaluate the experimental findings relating to the anti-cancer activity of this class of compounds has been made. The present review fills this gap in the literature and discusses both natural and synthetic phenazines with a critical focus on in vitro, in vivo and available clinical anti-cancer activities of these compounds.
引用
收藏
页码:487 / 501
页数:15
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