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Bacterial Lipopolysaccharides Induce Steroid Sulfatase Expression and Cell Migration through IL-6 Pathway in Human Prostate Cancer Cells

Authors
Im, Hee-JungPark, Na-HeeKwon, Yeo-JungShin, SangyunKim, DonghakChun, Young-Jin
Issue Date
30-Nov-2012
Publisher
KOREAN SOC APPLIED PHARMACOLOGY
Keywords
Steroid sulfatase; Lipopolysaccharides; Interleukin-6; Tumor cell migration; PC-3
Citation
BIOMOLECULES & THERAPEUTICS, v.20, no.6, pp 556 - 561
Pages
6
Journal Title
BIOMOLECULES & THERAPEUTICS
Volume
20
Number
6
Start Page
556
End Page
561
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/20012
DOI
10.4062/biomolther.2012.20.6.556
ISSN
1976-9148
2005-4483
Abstract
Steroid sulfatase (STS) is responsible for the conversion of estrone sulfate to estrone that can stimulate growth in endocrine-dependent tumors such as prostate cancer. Although STS is considered as a therapeutic target for the estrogen-dependent diseases, cellular function of STS are still not clear. Previously, we found that tumor necrosis factor (TNF)-alpha significantly enhances steroid sulfatase expression in PC-3 human prostate cancer cells through PI3K/Akt-dependent pathways. Here, we studied whether bacterial lipopolysaccharides (LPS) which are known to induce TNF-alpha may increase STS expression. Treatment with LPS in PC-3 cells induced STS mRNA and protein in concentration- and time-dependent manners. Using luciferase reporter assay, we found that LPS enhanced STS promoter activity. Moreover, STS expression induced by LPS increased PC-3 tumor cell migration determined by wound healing assay. We investigated that LPS induced IL-6 expression and IL-6 increased STS expression. Taken together, these data strongly suggest that LPS induces STS expression through IL-6 pathway in human prostate cancer cells.
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