首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Sanguinarine-induced G1-phase arrest of the cell cycle results from increased p27KIP1 expression mediated via activation of the Ras/ERK signaling pathway in vascular smooth muscle cells
Authors:Lee Beobyi  Lee Se-Jung  Park Sung-Soo  Kim Si-Kwan  Kim Sung-Ryong  Jung Jae-Hyun  Kim Wun-Jae  Moon Sung-Kwon
Institution:a Department of Anatomy, College of Medicine, Konkuk University, Chungju City, Chungbuk 380-701, South Korea
b Cheju Traditional Food Institute, Cheju Halla College, Nohyung-dong 1534, Jeju-si, Jeju-do, South Korea
c Department of Life Science, College of Biomedical and Health Science, Konkuk University, Chungju, Chungbuk 380-701, South Korea
d Department of Polymer Science and Engineering, College of Science and Technology, Chungju National University, Chungju, Chungbuk 380-702, South Korea
e Department of Urology, Chungbuk National University College of Medicine, Cheongju, Chungbuk 361-763, South Korea
f Department of Food and Biotechnology, Chungju National University, 123 Geomdan-ri Iryu-myeon, Chungju, Chungbuk 380-702, South Korea
Abstract:The present study identified a novel mechanism for the effects of sanguinarine in vascular smooth muscle cells (VSMC). Sanguinarine treatment of VSMC resulted in significant growth inhibition as a result of G1-phase cell-cycle arrest mediated by induction of p27KIP1 expression, and resulted in a down-regulation of the expression of cyclins and CDKs in VSMC. Moreover, sanguinarine-induced inhibition of cell growth appeared to be linked to activation of Ras/ERK through p27KIP1-mediated G1-phase cell-cycle arrest. Overall, the unexpected effects of sanguinarine treatment in VSMC provide a theoretical basis for clinical use of therapeutic agents in the treatment of atherosclerosis.
Keywords:Sanguinarine  VSMC  ERK  G1-phase cell-cycle arrest  p27  Ras
本文献已被 ScienceDirect PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号