Interferon regulatory factor-1 (IRF-1) regulates VEGF-induced angiogenesis in HUVECs

被引:21
|
作者
Lee, Jeong Heon [3 ]
Chun, Taehoon [4 ]
Park, Sang-Yoon [2 ]
Rho, Seung Bae [1 ]
机构
[1] Natl Canc Ctr, Res Inst, Goyang Si 411769, Gyeonggi Do, South Korea
[2] Natl Canc Ctr, Dept Obstet & Gynecol, Res Inst, Goyang 411769, Gyeonggi, South Korea
[3] Chonbuk Natl Univ, Dept Obstet & Gynecol, Sch Med, Jeonju 561712, South Korea
[4] Korea Univ, Div Biotechnol, Coll Life Sci & Biotechnol, Seoul 136701, South Korea
来源
关键词
interferon regulatory factor; angiogenesis; alternative splicing; endothelial cell; vessel sprouting; CAM;
D O I
10.1016/j.bbamcr.2008.04.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interferon regulatory factor-1 (IRF-1) is a tumor suppressor and transcriptional modulator that can regulate gene expression involved in cell growth control, induction of apoptosis, and post-translation modification. In this study, we found that IRF-1 inhibits endothelial cell angiogenesis using human umbilical vein endothelial cell (HUVECs) culture system. In addition, IRF-1 directly inhibited the tube formation of endothelial cells on Matrigel and reduced the expression of p-Akt, and p-eNOS, which play a significant role in angiogenesis when stimulated by VEGF. We also demonstrate that C-terminal region including transactivation domain (TA) of IRF-1 functions as a signal for its angiostatic activity, and is spliced in human tumor tissues. These findings indicate that splicing variant involving exons 7 of IRF-1 could potentially modulate anti-angiogenic effect of IRF-1. In overall, this study provides the first evidence for anti-angiogenic role of IRF-1, which may have therapeutic values for cancer and angiogenesis-associated diseases. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1654 / 1662
页数:9
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