3.8 Review

The hedgehog/Gli signaling paradigm in prostate cancer

Journal

EXPERT REVIEW OF ENDOCRINOLOGY & METABOLISM
Volume 6, Issue 3, Pages 453-467

Publisher

ROUTLEDGE JOURNALS, TAYLOR & FRANCIS LTD
DOI: 10.1586/EEM.11.24

Keywords

androgen signaling; cyclopamine; Gli; hedgehog signaling; prostate cancer; Smoothened

Funding

  1. United States Department of Defense Prostate Cancer Research Program [W81XH-10-10125, W81XH-10-1-0493, W81XH-060061]
  2. NIH [RO1-CA11618]
  3. NATIONAL CANCER INSTITUTE [R01CA111618] Funding Source: NIH RePORTER

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Hedgehog is a ligand-activated signaling pathway that regulates Gli-mediated transcription. Although most noted for its role as an embryonic morphogen, hyperactive hedgehog also causes human skin and brain malignancies. The hedgehog-related gene anomalies found in these tumors are rarely found in prostate cancer. Yet surveys of human prostate tumors show concordance of high expression of hedgehog ligands and Gli2 that correlate with the potential for metastasis and therapy-resistant behavior. Likewise, prostate cancer cell lines express hedgehog target genes, and their growth and survival is affected by hedgehog/Gli inhibitors. To date, the preponderance of data supports the idea that prostate tumors benefit from a paracrine hedgehog microenvironment similar to the developing prostate. Uncertainty remains as to whether hedgehog's influence in prostate cancer also includes aspects of tumor cell autocrine-like signaling. The recent findings that Gli proteins interact with the androgen receptor and affect its transcriptional output have helped to identify a novel pathway through which hedgehog/Gli might affect prostate tumor behavior and raises questions as to whether hedgehog signaling in prostate cancer cells is suitably measured by the expression of Gli target genes alone.

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