A Role for Class 3 Semaphorins in Prostate Cancer

被引:42
|
作者
Blanc, V.
Nariculam, J.
Munson, P. [2 ]
Freeman, A. [2 ]
Klocker, H. [3 ]
Masters, J.
Williamson, M. [1 ]
机构
[1] UCL, Prostate Canc Res Ctr, Dept Surg & Intervent Sci, London W1W 7EJ, England
[2] UCL, Dept Histopathol, London W1W 7EJ, England
[3] Innsbruck Med Univ, Dept Urol, Innsbruck, Austria
来源
PROSTATE | 2011年 / 71卷 / 06期
关键词
sema3E; plexin; neuropilin; hypoxia; TUMOR-SUPPRESSOR; RECEPTOR PLEXIN-B1; INVASIVE GROWTH; LUNG-CANCER; TRANSMEMBRANE; ATTRACTION; ACTIVATION; EXPRESSION; REPULSION; INTERACTS;
D O I
10.1002/pros.21281
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND. Class 3 semaphorins are secreted proteins that act as guidance cues for migrating cells via their transmembrane receptors plexins and neuropilins. Semaphorins have a role in cancer affecting tumor progression both directly, and indirectly by affecting angiogenesis. METHODS. The expression of semaphorins and their receptors in prostate cancer cell lines and tissue was determined by RT-PCR, Western blotting and immunohistochemistry. The effect of Sema3E on prostate cancer cell lines was determined by adhesion assays and transwell migration assays. RESULTS. Semaphorins and their receptors, plexins and neuropilins, are widely co-expressed in prostate cancer cell lines and tissue with a significant overexpression of Sema3E in tumor tissue. Sema3E affected integrin-mediated adhesion to fibronectin of prostate cancer cells, and inhibited their motility. Expression of Sema3C was upregulated and Sema3A and Sema3E were down regulated in prostate cells by hypoxia, consistent with an additional role for Sema3A and 3E as anti-angiogenic factors in prostate cancer. CONCLUSIONS. Semaphorin 3E is aberrantly expressed in prostate cancer and affects adhesion and motility of prostate cancer cells, indicating a role for the Sema3E/PlexinD1 signaling pathway in prostate cancer and identifying a new possible target for therapy. Prostate 71: 649-658, 2011. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:649 / 658
页数:10
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