The hedgehog/Gli signaling paradigm in prostate cancer

被引:42
作者
Chen, Mengqian [1 ]
Carkner, Richard [1 ]
Buttyan, Ralph [1 ,2 ]
机构
[1] Ordway Res Inst, 150 New Scotland Ave, Albany, NY 12208 USA
[2] Albany Med Coll, Div Urol, New York, NY USA
关键词
androgen signaling; cyclopamine; Gli; hedgehog signaling; prostate cancer; Smoothened;
D O I
10.1586/EEM.11.24
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:453 / 467
页数:15
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