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Therapeutic potential of ghrelin and des-acyl ghrelin against chemotherapy-induced cardiotoxicity.
Nonaka, Miki; Kurebayashi, Nagomi; Murayama, Takashi; Sugihara, Masami; Terawaki, Kiyoshi; Shiraishi, Seiji; Miyano, Kanako; Hosoda, Hiroshi; Kishida, Shosei; Kangawa, Kenji; Sakurai, Takashi; Uezono, Yasuhito.
Affiliation
  • Nonaka M; Division of Cancer Pathophysiology, National Cancer Center Research Institute, Tokyo 104-0045, Japan.
  • Kurebayashi N; Department of Cellular and Molecular Pharmacology, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan.
  • Murayama T; Department of Cellular and Molecular Pharmacology, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan.
  • Sugihara M; Department of Clinical Laboratory Medicine, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan.
  • Terawaki K; Division of Cancer Pathophysiology, National Cancer Center Research Institute, Tokyo 104-0045, Japan.
  • Shiraishi S; Tsumura Kampo Research Laboratories, Kampo Research & Development Division, Tsumura & Co., Ibaraki 300-1192, Japan.
  • Miyano K; Division of Cancer Pathophysiology, National Cancer Center Research Institute, Tokyo 104-0045, Japan.
  • Hosoda H; Division of Cancer Pathophysiology, National Cancer Center Research Institute, Tokyo 104-0045, Japan.
  • Kishida S; Department of Regenerative Medicine and Tissue Engineering, National Cerebral and Cardiovascular Center Research Institute, Suita 565-8565, Japan.
  • Kangawa K; Department of Biochemistry and Genetics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8544, Japan.
  • Sakurai T; National Cerebral and Cardiovascular Center Research Institute, Suita 565-8565, Japan.
  • Uezono Y; Department of Cellular and Molecular Pharmacology, Juntendo University Graduate School of Medicine, Tokyo 113-8421, Japan.
Endocr J ; 64(Suppl.): S35-S39, 2017.
Article in En | MEDLINE | ID: mdl-28652542
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Doxorubicin / Protective Agents / Ghrelin / Cardiotoxicity / Heart / Antineoplastic Agents Aspects: Patient_preference Limits: Animals Language: En Journal: Endocr J Journal subject: ENDOCRINOLOGIA Year: 2017 Document type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Doxorubicin / Protective Agents / Ghrelin / Cardiotoxicity / Heart / Antineoplastic Agents Aspects: Patient_preference Limits: Animals Language: En Journal: Endocr J Journal subject: ENDOCRINOLOGIA Year: 2017 Document type: Article Affiliation country: Japan