Journal
CELL CYCLE
Volume 6, Issue 22, Pages 2810-2816Publisher
LANDES BIOSCIENCE
DOI: 10.4161/cc.6.22.4947
Keywords
VHL; HIF-2 alpha; HIF-3 alpha 4; IPAS; RCC
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The most prevalent mutations associated with the development of clear-cell renal cell carcinoma (CC-RCC) are the loss-of-function mutations of von Hippel-Lindau (VHL) tumor suppressor gene. These mutations invariably result in an inappropriate accumulation of HIF-alpha due to a failure of VHL as a substrate-recognition component of an E3 ubiquitin ligase complex to target HIF-alpha for oxygen-dependent ubiquitin-mediated destruction. Stabilization of HIF-2 alpha, but not HIF-1 alpha, is the critical oncogenic event upon the functional loss of VHL in the development of CC-RCC. Here, we show that HIF-3 alpha 4, an alternatively spliced variant of human HIF-3 alpha with similar domain structure as the murine inhibitory PAS protein (IPAS), forms an abortive transcriptional complex with HIF-2 alpha and prevents the engagement of HIF-2 to the hypoxia-responsive elements (HREs) located in the promoter/enhancer regions of hypoxia-inducible genes. In addition, the re-expression of HIF-3 alpha 4 in VHL-null 786-O CC-RCC cells via adenovirus decreases the endogenous expression of HIF-2-driven gene expression and suppresses the growth of 786-O tumor xenografts in SCID mice. These results suggest that HIF-3 alpha 4 is a naturally occurring dominant-negative HIF-3 alpha splice isoform with tumor suppressive activity and support the targeted delivery of HIF-3 alpha 4 as a potential therapeutic option to curtail HIF-dependent tumor progression.
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