Cancer Treatment-Induced Cardiotoxicity: A Cardiac Stem Cell Disease?

L. Prezioso, S. Tanzi, F. Galaverna, C. Frati, B. Testa, M. Savi, G. Graiani, C. Lagrasta, S. Cavalli, S. Galati, D. Madeddu, E. Lodi Rizzini, F. Ferraro, E. Musso, D. Stilli, K. Urbanek, E. Piegari, A. De Angelis, A. Maseri, F. RossiE. Quaini, F. Quaini

Research output: Contribution to journalReview articlepeer-review

23 Scopus citations


Cardiovascular diseases and cancer represent respectively the first and second cause of death in industrialized countries. These two conditions may become synergistic when cardiovascular complications of anti-cancer therapy are considered. More than 70% of childhood and 50% of adult cancer patients can be cured, however this important success obtained by the biological and medical research is obfuscated by emerging findings of early and late morbidity due to cardiovascular events. Although anthracyclines are effective drugs against cancer a dose-dependent cardiotoxic effects whose mechanism has not been elucidated resulting in failure of therapeutic interventions limit their use. Unexpectedly, tyrosine/kinase inhibitors (TKIs) aimed at molecularly interfering with oncogenic pathways, have been implicated in cardiac side effects. Possible explanations of this phenomenon have been ambiguous, further strengthening the need to deepen our understanding on the mechanism of cardiotoxicity. In addition to a detailed description of anthracyclines and TKIs-related cardiovascular effects, the present review highlights recent observations supporting the hypothesis that the cellular target of anthracyclines and TKIs may include myocardial compartments other than parenchymal cells. The demonstration that the adult mammalian heart possesses a cell turnover regulated by primitive cells suggests that this cell population may be implicated in the onset and development of cardiovascular effects of anti-cancer strategies. The possibility of preventing cardiotoxicity by preservation and/or expansion of the resident stem cell pool responsible for cardiac repair may open new therapeutic options to unravel an unsolved clinical issue.

Original languageEnglish
Pages (from-to)55-75
Number of pages21
JournalCardiovascular and Hematological Agents in Medicinal Chemistry
Issue number1
StatePublished - Jan 2010


  • Anthracycline
  • Cancer treatment
  • Cardiac progenitors
  • Cardiotoxicity
  • Cardiovascular diseases
  • Regenerative medicine
  • Stem cells
  • Tyrosine kinase inhibitors


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