Cardiac glycosides as novel cancer therapeutic agents

被引:401
作者
Newman, Robert A. [1 ,2 ]
Yang, Peiying [1 ,2 ]
Pawlus, Alison D. [1 ,2 ]
Block, Keith I. [3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Houston, TX 77054 USA
[2] Univ Texas MD Anderson Canc Ctr, Pharmaceut Dev Ctr, Houston, TX 77054 USA
[3] Inst Integrat Canc Care, Evanston, IL 60201 USA
关键词
D O I
10.1124/mi.8.1.8
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
The class of steroid- like compounds designated cardiac glycosides includes well- known drugs such as digoxin, digitoxin, and ouabain. Their continued efficacy in treatment of congestive heart failure and as anti- arrhythmic agents is well appreciated. Less well known, however, is the emerging role of this category of compounds in the prevention and/ or treatment of proliferative diseases such as cancer. New findings within the past five years have revealed these compounds to be involved in complex cell- signal transduction mechanisms, resulting in selective control of human tumor but not normal cellular proliferation. As such, they represent a promising form of targeted cancer chemotherapy. New clinical studies of their anticancer potential as single or adjuvant treatments may provide insight into these potentially valuable therapeutic options. This review focuses on recent findings on cellular pharmacology of cardiac glycosides as they relate to treatment of human cancer and attempts to explain why these agents have been overlooked in the past.
引用
收藏
页码:36 / 49
页数:14
相关论文
共 116 条
[91]   Antiproliferative cardenolides from Periploca graeca [J].
Spera, Daniela ;
Siciliano, Tiziana ;
De Tommasi, Nunziatina ;
Braca, Alessandra ;
Vessieres, Anne .
PLANTA MEDICA, 2007, 73 (04) :384-387
[92]   Oleandrin suppresses activation of nuclear transcription factor-κB and activator protein-1 and potentiates apoptosis induced by ceramide [J].
Sreenivasan, Y ;
Sarkar, A ;
Manna, SK .
BIOCHEMICAL PHARMACOLOGY, 2003, 66 (11) :2223-2239
[93]   RETRACTED: Oleandrin-mediated expression of fas potentiates apoptosis in tumor cells (Retracted article. See vol. 33, pg. 1031, 2013) [J].
Sreenivasan, Yashin ;
Raghavendra, Pongali B. ;
Manna, Sunil K. .
JOURNAL OF CLINICAL IMMUNOLOGY, 2006, 26 (04) :308-322
[94]  
Stenkvist B, 1999, ONCOL REP, V6, P493
[95]  
STENKVIST B, 1979, LANCET, V1, P563
[96]  
Svensson Å, 2005, ANTICANCER RES, V25, P207
[97]   Constituents of the Vietnamese medicinal plant Streptocaulon juventas and their antiproliferative activity against the human HT-1080 fibrosarcoma cell line [J].
Ueda, J ;
Tezuka, Y ;
Banskota, AH ;
Le Tran, Q ;
Tran, QK ;
Saiki, I ;
Kadota, S .
JOURNAL OF NATURAL PRODUCTS, 2003, 66 (11) :1427-1433
[98]  
UJHELYI MR, 1994, ANN INTERN MED, V120, P247, DOI 10.7326/0003-4819-120-3-199402010-00015
[99]  
Umebayashi C, 2003, BIOL PHARM BULL, V26, P627, DOI 10.1248/bpb.26.627
[100]   Identification of a novel cardenolide (2"-oxovoruscharin) from Calotropis procera and the hemisynthesis of novel derivatives displaying potent in vitro antitumor activities and high in vivo tolerance:: Structure-activity relationship analyses [J].
Van Quaquebeke, E ;
Simon, G ;
André, A ;
Dewelle, J ;
El Yazidi, M ;
Bruyneel, F ;
Tuti, J ;
Nacoulma, O ;
Guissou, P ;
Decaestecker, C ;
Braekman, JC ;
Kiss, R ;
Darro, F .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (03) :849-856