Repurposing of approved cardiovascular drugs

被引:74
作者
Ishida, Junichi [1 ]
Konishi, Masaaki [1 ]
Ebner, Nicole [1 ]
Springer, Jochen [1 ]
机构
[1] Univ Med Ctr Gottingen, Dept Cardiol & Pneumol, Innovat Clin Trials, Robert Koch Str 40, D-37075 Gottingen, Germany
关键词
Drug repurposing; Drug repositioning; Cardiovascular drugs; Second label indication; Pleiotropic properties; CONVERTING ENZYME-INHIBITORS; ENDOTHELIAL GROWTH-FACTOR; II TYPE-1 RECEPTOR; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; SYMPATHETIC-NERVOUS-SYSTEM; BETA-ADRENERGIC-RECEPTORS; CANCER CELL-LINES; HMG-COA REDUCTASE; BREAST-CANCER; CARDIAC-GLYCOSIDES;
D O I
10.1186/s12967-016-1031-5
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
Research and development of new drugs requires both long time and high costs, whereas safety and tolerability profiles make the success rate of approval very low. Drug repurposing, applying known drugs and compounds to new indications, has been noted recently as a cost-effective and time-unconsuming way in developing new drugs, because they have already been proven safe in humans. In this review, we discuss drug repurposing of approved cardiovascular drugs, such as aspirin, beta-blockers, angiotensin converting enzyme inhibitors, angiotensin II receptor blockers, cardiac glycosides and statins. Regarding anti-tumor activities of these agents, a number of experimental studies have demonstrated promising pleiotropic properties, whereas all clinical trials have not shown expected results. In pathological conditions other than cancer, repurposing of cardiovascular drugs is also expanding. Numerous experimental studies have reported possibilities of drug repurposing in this field and some of them have been tried for new indications ('bench to bedside'), while unexpected results of clinical studies have given hints for drug repurposing and some unknown mechanisms of action have been demonstrated by experimental studies ('bedside to bench'). The future perspective of experimental and clinical studies using cardiovascular drugs are also discussed.
引用
收藏
页数:15
相关论文
共 159 条
[11]   Digoxin use and the risk of cancers of the corpus uteri, ovary and cervix [J].
Biggar, Robert J. ;
Wohlfahrt, Jan ;
Melbye, Mads .
INTERNATIONAL JOURNAL OF CANCER, 2012, 131 (03) :716-721
[12]   Digoxin Use and the Risk of Breast Cancer in Women [J].
Biggar, Robert J. ;
Wohlfahrt, Jan ;
Oudin, Anna ;
Hjuler, Thomas ;
Melbye, Mads .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (16) :2165-2170
[13]   3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors and the risk of cancer -: A nested case-control study [J].
Blais, L ;
Desgagné, A ;
LeLorier, J .
ARCHIVES OF INTERNAL MEDICINE, 2000, 160 (15) :2363-2368
[14]   Carvedilol for Portal Hypertension in Patients with Cirrhosis [J].
Bosch, Jaime .
HEPATOLOGY, 2010, 51 (06) :2214-2218
[15]   Aspirin and cancer risk: a quantitative review to 2011 [J].
Bosetti, C. ;
Rosato, V. ;
Gallus, S. ;
Cuzick, J. ;
La Vecchia, C. .
ANNALS OF ONCOLOGY, 2012, 23 (06) :1403-1415
[16]   Angiotensin II blockade and aortic-root dilation in Marfan's syndrome [J].
Brooke, Benjamin S. ;
Habashi, Jennifer P. ;
Judge, Daniel P. ;
Patel, Nishant ;
Loeys, Bart ;
Dietz, Harry C., III .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (26) :2787-2795
[17]   POTASSIUM CHANNEL CONDUCTANCE - A MECHANISM AFFECTING HAIR-GROWTH BOTH INVITRO AND INVIVO [J].
BUHL, AE ;
WALDON, DJ ;
CONRAD, SJ ;
MULHOLLAND, MJ ;
SHULL, KL ;
KUBICEK, MF ;
JOHNSON, GA ;
BRUNDEN, MN ;
STEFANSKI, KJ ;
STEHLE, RG ;
GADWOOD, RC ;
KAMDAR, BV ;
THOMASCO, LM ;
SCHOSTAREZ, HJ ;
SCHWARTZ, TM ;
DIANI, AR .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1992, 98 (03) :315-319
[18]   DEPRESSION IN HOSPITALIZED CANCER-PATIENTS [J].
BUKBERG, J ;
PENMAN, D ;
HOLLAND, JC .
PSYCHOSOMATIC MEDICINE, 1984, 46 (03) :199-212
[19]   Sodium/potasium ATPase (Na+, K+-ATPase) and ouabain/related cardiac glycosides:: a new paradigm for development of anti-breast cancer drugs? [J].
Chen, JQ ;
Contreras, RG ;
Wang, R ;
Fernandez, SV ;
Shoshani, L ;
Russo, IH ;
Cereijido, M ;
Russo, J .
BREAST CANCER RESEARCH AND TREATMENT, 2006, 96 (01) :1-15
[20]   Do stress-related psychosocial factors contribute to cancer incidence and survival? [J].
Chida, Yoichi ;
Hamer, Mark ;
Wardle, Jane ;
Steptoe, Andrew .
NATURE CLINICAL PRACTICE ONCOLOGY, 2008, 5 (08) :466-475