HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Cardiotoxicity of the cancer therapeutic agent imatinib mesylate.

Abstract
Imatinib mesylate (Gleevec) is a small-molecule inhibitor of the fusion protein Bcr-Abl, the causal agent in chronic myelogenous leukemia. Here we report ten individuals who developed severe congestive heart failure while on imatinib and we show that imatinib-treated mice develop left ventricular contractile dysfunction. Transmission electron micrographs from humans and mice treated with imatinib show mitochondrial abnormalities and accumulation of membrane whorls in both vacuoles and the sarco- (endo-) plasmic reticulum, findings suggestive of a toxic myopathy. With imatinib treatment, cardiomyocytes in culture show activation of the endoplasmic reticulum (ER) stress response, collapse of the mitochondrial membrane potential, release of cytochrome c into the cytosol, reduction in cellular ATP content and cell death. Retroviral gene transfer of an imatinib-resistant mutant of c-Abl, alleviation of ER stress or inhibition of Jun amino-terminal kinases, which are activated as a consequence of ER stress, largely rescues cardiomyocytes from imatinib-induced death. Thus, cardiotoxicity is an unanticipated side effect of inhibition of c-Abl by imatinib.
AuthorsRisto Kerkelä, Luanda Grazette, Rinat Yacobi, Cezar Iliescu, Richard Patten, Cara Beahm, Brian Walters, Sergei Shevtsov, Stéphanie Pesant, Fred J Clubb, Anthony Rosenzweig, Robert N Salomon, Richard A Van Etten, Joseph Alroy, Jean-Bernard Durand, Thomas Force
JournalNature medicine (Nat Med) Vol. 12 Issue 8 Pg. 908-16 (Aug 2006) ISSN: 1078-8956 [Print] United States
PMID16862153 (Publication Type: Comparative Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Benzamides
  • Piperazines
  • Pyrimidines
  • Imatinib Mesylate
  • Cytochromes c
  • Adenosine Triphosphatases
  • Calcium
Topics
  • Adenosine Triphosphatases (analysis, metabolism)
  • Animals
  • Antineoplastic Agents (administration & dosage, adverse effects, pharmacology, toxicity)
  • Benzamides
  • Calcium (metabolism)
  • Cell Death (drug effects)
  • Cell Membrane Permeability (drug effects)
  • Cells, Cultured
  • Cytochromes c (metabolism)
  • Dose-Response Relationship, Drug
  • Echocardiography
  • Heart Failure (chemically induced, pathology)
  • Humans
  • Imatinib Mesylate
  • Injections, Intraperitoneal
  • Membrane Potentials (drug effects)
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria, Heart (drug effects, pathology, ultrastructure)
  • Mitochondrial Membranes (drug effects)
  • Myocytes, Cardiac (drug effects, pathology, ultrastructure)
  • Piperazines (administration & dosage, adverse effects, pharmacology, toxicity)
  • Pyrimidines (administration & dosage, adverse effects, pharmacology, toxicity)
  • Sarcoplasmic Reticulum (drug effects, pathology, ultrastructure)
  • Severity of Illness Index
  • Time Factors
  • Ventricular Dysfunction, Left (chemically induced, physiopathology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: