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Novel molecular mechanisms and regeneration therapy for heart failure.
Oka, Toru; Morita, Hiroyuki; Komuro, Issei.
Afiliação
  • Oka T; Onco-Cardiology Unit, Department of Cardiology, Osaka Medical Center for Cancer and Cardiovascular Diseases, 1-3-3 Nakamichi, Higashinari-ku, Osaka 537-8511, Japan; Japan Science and Technology Agency, CREST, Tokyo, Japan. Electronic address: oka-to@mc.pref.osaka.jp.
  • Morita H; Department of Cardiovascular Medicine, The University of Tokyo Graduate School of Medicine, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.
  • Komuro I; Japan Science and Technology Agency, CREST, Tokyo, Japan; Department of Cardiovascular Medicine, The University of Tokyo Graduate School of Medicine, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan. Electronic address: komuro-tky@umin.ac.jp.
J Mol Cell Cardiol ; 92: 46-51, 2016 Mar.
Article em En | MEDLINE | ID: mdl-26829118
ABSTRACT
Heart failure (HF) is one of the leading causes of mortality in the world. Various molecular mechanisms have been proposed for HF, but its precise mechanisms are still largely unknown. In this review, summarizing the "President's Distinguished Lecture Award" of XX World Congress of International Society for Heart Research 2010 in Kyoto, Japan, we introduce recent our studies on HF, including 1) p53-induced suppression of Hif-1-induced angiogenesis as a novel mechanism of HF, 2) angiogenesis as a potential therapeutic strategy for HF, and 3) IGFBP-4 as a novel factor for cardiomyogenesis by inhibiting canonical Wnt signaling.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Insuficiência Cardíaca / Neovascularização Patológica Limite: Humans Idioma: En Revista: J Mol Cell Cardiol Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Insuficiência Cardíaca / Neovascularização Patológica Limite: Humans Idioma: En Revista: J Mol Cell Cardiol Ano de publicação: 2016 Tipo de documento: Article