| Literature DB >> 28652542 |
Miki Nonaka1, Nagomi Kurebayashi2, Takashi Murayama2, Masami Sugihara3, Kiyoshi Terawaki1,4, Seiji Shiraishi1, Kanako Miyano1, Hiroshi Hosoda5, Shosei Kishida6, Kenji Kangawa7, Takashi Sakurai2, Yasuhito Uezono1,8.
Abstract
Cancer was considered an incurable disease for many years; however, with the development of anticancer drugs and state-of-the art technologies, it has become curable. Cardiovascular diseases in patients with cancer or induced by cancer chemotherapy have recently become a great concern. Certain anticancer drugs and molecular targeted therapies cause cardiotoxicity, which limit the widespread implementation of cancer treatment and decrease the quality of life in cancer patients significantly. The anthracycline doxorubicin (DOX) causes cardiotoxicity. The cellular mechanism underlying DOX-induced cardiotoxicity include free-radical damage to cardiac myocytes, leading to mitochondrial injury and subsequent death of myocytes. Recently, circulating orexigenic hormones, ghrelin and des-acyl ghrelin, have been reported to inhibit DOX-induced cardiotoxicity. However, little is known about the molecular mechanisms underlying their preventive effects. In the present study, we show the possible mechanisms underlying the effects of ghrelin and des-acyl ghrelin against DOX-induced cardiotoxicity through in vitro and in vivo researches.Entities:
Keywords: Cardiotoxicity; Chemotherapy; Des-acyl ghrelin; Doxorubicin; Ghrelin
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Year: 2017 PMID: 28652542 DOI: 10.1507/endocrj.64.S35
Source DB: PubMed Journal: Endocr J ISSN: 0918-8959 Impact factor: 2.349