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Inflammation-mediated abrogation of androgen signaling: An in vitro model of prostate cell inflammation

Authors

  • Bilge Debelec-Butuner,

    1. Department of Pharmaceutical Biotechnology, Ege University, Bornova, Izmir, Turkey
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  • Cansu Alapinar,

    1. Department of Bioengineering, Cancer Biology Laboratory, Ege University, Bornova, Izmir, Turkey
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  • Lokman Varisli,

    1. Department of Bioengineering, Cancer Biology Laboratory, Ege University, Bornova, Izmir, Turkey
    Current affiliation:
    1. Faculty of Science, Department of Biology, Osmanbey Campus, Harran University, Sanliurfa, Turkey
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  • Burcu Erbaykent-Tepedelen,

    1. Department of Bioengineering, Cancer Biology Laboratory, Ege University, Bornova, Izmir, Turkey
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  • Syed Muhammad Hamid,

    1. Department of Bioengineering, Cancer Biology Laboratory, Ege University, Bornova, Izmir, Turkey
    Current affiliation:
    1. Faculty of Science, Department of Molecular Biology, Izmir Institute of Technology, Gulbahce, Izmir, Turkey
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  • Ceren Gonen-Korkmaz,

    1. Department of Pharmacology, Ege University, Bornova, Izmir, Turkey
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  • Kemal Sami Korkmaz

    Corresponding author
    1. Department of Bioengineering, Cancer Biology Laboratory, Ege University, Bornova, Izmir, Turkey
    • Correspondence to: Cancer Biology Laboratory, Department of Bioengineering, Ege University, Bornova, Izmir, Turkey.

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Abstract

As a link between inflammation and cancer has been reported in many studies, we established an in vitro model of prostatic inflammation to investigate the loss of androgen receptor (AR)-mediated signaling in androgen responsive prostate cell lines. First, the U937 monocyte cell line was differentiated into macrophages using phorbol acetate (PMA), and cells were induced with lipopolysaccharide (LPS) for cytokine secretion. Next, the cytokine levels (TNFα, IL-6, and IL1β) in conditioned media (CM) were analyzed. Prostate cells were then fed with CM containing varying concentrations of TNFα, and IkB degradation, nuclear factor kappa B (NFκB) translocation and transactivation, and the expression of matrix metalloproteinase-8 (MMP8) and matrix metalloproteinase-9 (MMP9) were then assessed. As a result of CM treatment, ubiquitin-mediated AR degradation, which was restored using anti-TNFα antibody neutralization, led to both a decrease in KLK4, PSA, and NKX3.1 expression levels and the upregulation of GPX2. In addition to the loss of AR, acute and chronic CM exposure resulted in p53 degradation and consequent p21 downregulation, which was also restored by either androgen administration or ectopic NKX3.1 expression via the stabilization of MDM2 levels in LNCaP cells. Additionally, CM treatment enhanced H2AX(S139) phosphorylation (a hallmark of DNA damage) and genetic heterogeneity in the absence of androgens in prostate cells without activating mitochondrial apoptosis. Thus, the data suggest that inflammatory cytokine exposure results in the loss of AR and p53 signaling in prostate cells and facilitates genetic heterogeneity via ROS accumulation to promote prostate carcinogenesis. © 2012 Wiley Periodicals, Inc.

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