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Multiple roles of KLF15 in the heart: Underlying mechanisms and therapeutic implications.
Zhao, Yuguang; Song, Wenjing; Wang, Lizhe; Rane, Madhavi J; Han, Fujun; Cai, Lu.
Afiliación
  • Zhao Y; Cancer Center, The First Hospital of Jilin University, Changchun, Jilin 130021, China.
  • Song W; Cancer Center, The First Hospital of Jilin University, Changchun, Jilin 130021, China.
  • Wang L; Department of Pediatric Oncology, The First Hospital of Jilin University, Changchun, Jilin 130021, China.
  • Rane MJ; Departments of Medicine, Biochemistry and Molecular Genetics, University of Louisville, Louisville, KY 40292, USA.
  • Han F; Cancer Center, The First Hospital of Jilin University, Changchun, Jilin 130021, China. Electronic address: fujun_han@aliyun.com.
  • Cai L; Pediatric Research Institute, Departments of Pediatrics, Radiation Oncology, Pharmacology and Toxicology, University of Louisville, Louisville, KY 40292, USA. Electronic address: L0cai001@louisville.edu.
J Mol Cell Cardiol ; 129: 193-196, 2019 04.
Article en En | MEDLINE | ID: mdl-30831134
ABSTRACT
Although there is an increasing understanding of the signaling pathways that promote cardiac hypertrophy, negative regulatory factors of this process have received less attention. Increasing evidence indicates that Krüppel-like factor 15 (KLF15) plays an important role in maintaining cardiac function by controlling the transcriptional pathways that regulating cardiac metabolism. Recent studies have also revealed a vital role for KLF15 as an inhibitor of pathological cardiac hypertrophy and fibrosis via its effects on factors such as myocyte enhancer factor 2 (MEF2), GATA-binding protein 4 (GATA4), transforming growth factor-ß (TGF-ß), and myocardin. KLF15 may therefore be an effective therapeutic target for the treatment of heart failure and other cardiovascular diseases. In this review, we focus on the physiological and pathophysiological roles of KLF15 in the heart and the potential mechanisms through which KLF15 is regulated in various cardiac diseases.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Factores de Transcripción de Tipo Kruppel / Miocardio Límite: Animals / Humans Idioma: En Revista: J Mol Cell Cardiol Año: 2019 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Factores de Transcripción de Tipo Kruppel / Miocardio Límite: Animals / Humans Idioma: En Revista: J Mol Cell Cardiol Año: 2019 Tipo del documento: Article País de afiliación: China
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