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Estrogen interacts with estrogen receptor and SP proteins to control VEGF.

Women's Health Weekly

| April 01, 2004 | COPYRIGHT 2004 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2004 APR 1 - (NewsRx.com & NewsRx.net) -- Estrogen interacts with estrogen receptor and SP proteins to control VEGF.

"Vascular endothelial growth factor (VEGF) is expressed in multiple hormone-dependent cancer cells/tumors. Treatment of ZR-75 breast cancer cells with 17beta-estradiol (E[subscript]2) induced a greater than four-fold increase of VEGF mRNA levels. ZR-75 breast cancer cells were transfected with pVEGF1, a construct containing a -2018 to +50 VEGF promoter insert, and E[subscript]2-induced reporter gene (luciferase) activity," scientists in the United States report.

"Deletion and mutation analysis of the VEGF gene promoter identified a GC-rich region (-66 to -47) which was required for E[subscript]2-induced transactivation of pVEGF5, a construct containing the minimal promoter (-66 to +54) that exhibited E[subscript]2 responsiveness," wrote M. Stoner and colleagues, Texas A&M University, Department of Veterinary Physiology and Pharmacology.

"Interactions of nuclear proteins from ZR-75 cells with the proximal GC-rich region of the VEGF gene promoter were investigated by electrophoretic mobility shift and chromatin immunoprecipitation assays. The results demonstrate that both Sp1 and Sp3 proteins bound the GC-rich motif (-66 to +47), and estrogen receptor alpha (ERalpha) interactions were ...

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