中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Critical role of TRPC6 channels in VEGF-mediated angiogenesis

文献类型:期刊论文

作者Wang, Yizheng
刊名CANCER LETTERS
出版日期2009
卷号283期号:1页码:43-51
关键词TRPC6 Angiogenesis VEGF Proliferation Tube formation ENDOTHELIAL GROWTH-FACTOR VASCULAR-PERMEABILITY FACTOR RECEPTOR POTENTIAL CHANNELS CELL LUNG-CANCER CATION CHANNEL TUMOR ANGIOGENESIS PLUS CARBOPLATIN EPITHELIAL-CELLS CA2+ ENTRY IN-VIVO
ISSN号0304-3835
通讯作者Shen, F (reprint author), Mil Med Coll 2, Div Comprehens Treatment, Eastern Hepatobiliary Hosp, Shanghai 200438, Peoples R China,shenfengdfgd@yahoo.com.cn ; yzwang@ion.ac.cn
英文摘要Intracellular Ca(2+) signaling plays critical roles in VEGF-mediated angiogenesis. Transient receptor potential canonical (TRPC) channel 6, a Ca(2+)-permeable non-selective cation channel, can be activated by VEGF. Here, we report that TRPC6 is important for VEGF-mediated angiogenesis. Inhibition of TRPC6 in human umbilical vein endothelial cells (HUVECs) by pharmacological or genetic approaches arrested HUVECs at G2/M phase and suppressed VEGF-induced HUVEC proliferation and tube formation. Furthermore, inhibition of TRPCs abolished VEGF-, but not FGF-induced angiogenesis in the chick embryo chorioallantoic membrane. These results suggest that TRPC6 plays an important role in VEGF-mediated angiogenesis. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
学科主题Oncology
收录类别SCI
资助信息Shanghai Municipal Council for Science and Technology[064119530]; 973 Program[2006CB806600]; National Natural Science Foundation of China[30872989, 30621062]
语种英语
公开日期2012-07-13
源URL[http://ir.sibs.ac.cn/handle/331001/1640]  
专题上海神经科学研究所_神经所(总)
上海神经科学研究所_神经信号转导研究组
推荐引用方式
GB/T 7714
Wang, Yizheng. Critical role of TRPC6 channels in VEGF-mediated angiogenesis[J]. CANCER LETTERS,2009,283(1):43-51.
APA Wang, Yizheng.(2009).Critical role of TRPC6 channels in VEGF-mediated angiogenesis.CANCER LETTERS,283(1),43-51.
MLA Wang, Yizheng."Critical role of TRPC6 channels in VEGF-mediated angiogenesis".CANCER LETTERS 283.1(2009):43-51.

入库方式: OAI收割

来源:上海神经科学研究所

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