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Free keywords:
Animals
CHO Cells
Cell Line, Tumor
Cricetinae
Cricetulus
Ether-A-Go-Go Potassium Channels/*biosynthesis/*physiology
Female
*Gene Expression Regulation, Neoplastic
Homeostasis
Humans
Hypoxia
Hypoxia-Inducible Factor 1, alpha Subunit/*metabolism
Mice
Mice, SCID
NIH 3T3 Cells
*Neovascularization, Pathologic
Vascular Endothelial Growth Factor A/*metabolism
Abstract:
Ether-a-go-go-1 (Eag1) is a CNS-localized voltage-gated potassium channel that is found ectopically expressed in a majority of extracranial solid tumors. While circumstantial evidence linking Eag1 to tumor biology has been well established, the mechanisms by which the channel contributes to tumor progression remain elusive. In this study, we have used in vivo and in vitro techniques to identify a candidate mechanism. A mutation that eliminates ion permeation fails to completely abolish xenograft tumor formation by transfected cells, indicating that Eag1 contributes to tumor progression independently of its primary function as an ion channel. Our data suggest that Eag1 interferes with the cellular mechanism for maintaining oxygen homeostasis, increasing HIF-1 activity, and thereby VEGF secretion and tumor vascularization.
