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This version published online on July 25, 2002
Molecular Endocrinology, doi:10.1210/me.2002-0123
Molecular Endocrinology Vol. 0, No. 2002 200201231-
doi:10.1210/me.2002-0123
Copyright © 2002 by the Endocrine Society.
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Submitted on March 28, 2002
Accepted on July 5, 2002

Cloning and Characterization of a Novel Endothelial Promoter of the Human CYP19 (Aromatase P450) Gene that is Up-regulated in Breast Cancer Tissue

SIBY SEBASTIAN1, KAZUTO TAKAYAMA1, MAKIO SHOZU1, and SERDAR E. BULUN1*

1 Departments of Obstetrics and Gynecology and Molecular Genetics, University of Illinois at Chicago, Chicago, IL 60612, the Department of Obstetrics and Gynecology, Tohoku University School of Medicine, Sendai 980-8574, Japan, the Department of Obstetrics and Gynecology, School of Medicine, Kanazawa University, 13--1 Takara-machi, Kanazawa, Japan 920-0934 Present address: Department of Pathology, Duke University Medical Center 3712 Durham, NC 27710.

* To whom correspondence should be addressed. E-mail: sbulun{at}uic.edu.

Intratumoral expression of aromatase P450 (P450arom) promotes the growth of breast tumors via increased local estrogen concentration. We cloned a novel 101 bp untranslated first exon (I.7) that comprises the 5'-end of 29--54% of P450arom transcripts isolated from breast cancer tissues (n = 7). The levels of P450arom transcripts with exon I.7 were significantly increased in breast tumor tissues and adipose tissue adjacent to tumors. We identified a promoter immediately upstream of exon I.7 and mapped this to ~36 kb upstream of ATG translation start site of the CYP19 (P450arom) gene. Sequence analysis of I.7 revealed a TATA-less promoter containing an initiator, two consensus GATA sites, and cis-regulatory elements found in megakaryocytes and endothelial type promoters. Luciferase activity directed by the promoter I.7 sequence (-299/+81 bp was 4-fold greater than a minimum length promoter sequence (-35/+81 bp) in human microvascular endothelial cells (HMEC-1), but only 2-fold greater in MCF-7 breast malignant epithelial cells. There was no promoter activity in primary breast adipose fibroblasts. Site-directed mutations demonstrated that maximal basal promoter activity required two GATA motifs at -146/-141 bp and -196/-191 bp. Gel shift and DNase I footprinting assays demonstrated the binding of GATA-2 transcription factor but not GATA-1 to the -196/-191 bp region. Overexpression of GATA-2 in HMEC-1 cells increases promoter I.7 activity by 5-fold. In conclusion, promoter I.7 is a GATA-2-regulated endothelial promoter of the human CYP19 gene and may increase estrogen biosynthesis in vascular endothelial cells of breast cancer. The activity of this promoter may also be important for intracrine and paracrine effects of estrogen on blood vessels.


Key words: Breast cancer • estrogen biosynthesis • aromatase • CYP19 • endothelial cell • alternative promoter use • transcriptional regulation • GATA-2

NURSA Molecule Pages Link:

Ligands:   17β-Estradiol



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