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Cardiac Atrophy and Heart Failure In Cancer

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Journal Card Fail Rev
Date 2017 Aug 9
PMID 28785478
Citations 18
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Abstract

Functional changes in the heart in patients with cancer can be a result of both the disease itself and various cancer therapies, and limiting cardiac damage has become an increasingly important issue as survival rates in patients with cancer have improved. Processes involved in cancer-induced cardiac atrophy may include cardiomyocyte atrophy and apoptosis, decreased protein synthesis, increased autophagy and proteolysis via the ubiquitin-proteosome system. Further to direct effects of malignancy on the heart, several chemotherapeutic agents are known to affect the myocardium, in particular the anthracyclines. The aim of this report is to review the effects of cancer and cancer treatment on the heart and what is known about the underlying mechanisms. Furthermore, clinical strategies to limit and treat cancer-associated cardiac atrophy are discussed, emphasising the benefit of a multidisciplinary approach by cardiologists and oncologists to optimise models of care to improve outcomes for patients with cancer.

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References
1.
Zhang S, Liu X, Bawa-Khalfe T, Lu L, Lyu Y, Liu L . Identification of the molecular basis of doxorubicin-induced cardiotoxicity. Nat Med. 2012; 18(11):1639-42. DOI: 10.1038/nm.2919. View

2.
von Haehling S, Anker S . Cachexia as a major underestimated and unmet medical need: facts and numbers. J Cachexia Sarcopenia Muscle. 2011; 1(1):1-5. PMC: 3060651. DOI: 10.1007/s13539-010-0002-6. View

3.
Campos E, OConnell J, Malvestio L, Romano M, Ramos S, Celes M . Calpain-mediated dystrophin disruption may be a potential structural culprit behind chronic doxorubicin-induced cardiomyopathy. Eur J Pharmacol. 2011; 670(2-3):541-53. DOI: 10.1016/j.ejphar.2011.09.021. View

4.
Murphy K . The pathogenesis and treatment of cardiac atrophy in cancer cachexia. Am J Physiol Heart Circ Physiol. 2016; 310(4):H466-77. DOI: 10.1152/ajpheart.00720.2015. View

5.
Tian M, Asp M, Nishijima Y, Belury M . Evidence for cardiac atrophic remodeling in cancer-induced cachexia in mice. Int J Oncol. 2011; 39(5):1321-6. DOI: 10.3892/ijo.2011.1150. View