Warning: Undefined variable $zfal in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 525
Deprecated: str_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 525

Warning: Undefined variable $sterm in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 530
Warning: Undefined variable $sterm in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 531
  English Wikipedia
Nephropedia Template TP (
Twit Text
DeepDyve Pubget Overpricing |   
lüll Cardiac glycosides as novel cancer therapeutic agents Newman RA; Yang P; Pawlus AD; Block KIMol Interv 2008[Feb]; 8 (1): 36-49The 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.|Animals[MESH]|Antineoplastic Agents/chemistry/metabolism/pharmacology/*therapeutic use[MESH]|Apoptosis/drug effects[MESH]|Autophagy/drug effects[MESH]|Cardiac Glycosides/chemistry/metabolism/pharmacology/*therapeutic use[MESH]|Drug Design[MESH]|Growth Inhibitors/chemistry/metabolism/pharmacology[MESH]|Humans[MESH]|Mice[MESH]|Neoplasms/*drug therapy/prevention & control[MESH]|Rats[MESH]|Receptors, Estrogen/metabolism[MESH]|Signal Transduction[MESH]|Sodium-Potassium-Exchanging ATPase/physiology[MESH]|Species Specificity[MESH] |