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10.1186/s12967-016-1031-5

http://scihub22266oqcxt.onion/10.1186/s12967-016-1031-5
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C5029061!5029061 !27646033
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suck abstract from ncbi


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pmid27646033
      J+Transl+Med 2016 ; 14 (ä): 269
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  • Repurposing of approved cardiovascular drugs #MMPMID27646033
  • Ishida J ; Konishi M ; Ebner N ; Springer J
  • J Transl Med 2016[Sep]; 14 (ä): 269 PMID27646033 show ga
  • 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.
  • |*Drug Approval [MESH]
  • |*Drug Repositioning [MESH]
  • |Cardiovascular Agents/*therapeutic use [MESH]
  • |Humans [MESH]


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