c-Myc enhances colon cancer cell-mediated angiogenesis through the regulation of HIF-1α

被引:51
|
作者
Chen, Cheng [1 ]
Cai, Shaoxin [1 ]
Wang, Guihua [1 ]
Cao, Xiaonian [1 ]
Yang, Xi [1 ]
Luo, Xuelai [1 ]
Feng, Yongdong [1 ]
Hu, Junbo [1 ]
机构
[1] Huazhong Univ Sci & Technol, Canc Res Inst, Tongji Hosp, Wuhan 430030, Peoples R China
关键词
Angiogenesis; Colon cancer; c-Myc; HIF-1; alpha; VEGF; ENDOTHELIAL GROWTH-FACTOR; INDUCIBLE FACTOR-I; TRANSCRIPTION FACTOR; GENE-EXPRESSION; HYPOXIA; HIF-1; METABOLISM; ACTIVATION; MECHANISMS; APOPTOSIS;
D O I
10.1016/j.bbrc.2012.12.006
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
Angiogenesis plays a pivotal role in tumor growth. The hypoxia-inducible factor 1, alpha subunit (HIF-1 alpha)/vascular endothelial growth factor pathway is the most important pathway for regulating angiogenesis in the tumor microenvironment. c-Myc is an important oncogene that has many biological functions. In this study, we investigated the role of c-Myc in tumor angiogenesis. We found that the overexpression of c-Myc in colon cancer cells could promote the expression of HIF-1 alpha and that of vascular endothelial growth factor. Moreover, we found that c-Myc regulated HIF-1 alpha at the post-transcriptional level. The results revealed c-Myc-dependent regulation of HIF-1 alpha instead of HIF-1 alpha-dependent c-Myc regulation for the first time. They also showed that c-Myc was essential to regulate colon cancer cell-mediated angiogenesis and contributed to tumor growth. This research provides the theoretical basis for clinical trials of new therapeutic targets of c-Myc and HIF-1 alpha in colon cancer cells. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:505 / 511
页数:7
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