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LEF1 in Androgen-Independent Prostate Cancer: Regulation of Androgen Receptor Expression, Prostate Cancer Growth, and Invasion

Departments of ¹ Pathology, ² Medicine, and ³ Urology, New York University School of Medicine, ⁴ New York Harbor Healthcare System, New York, New York; and ⁵ Department of Urology, University of California Los Angeles, Los Angeles, California

Requests for reprints: Peng Lee, Department of Pathology, New York University School of Medicine, 423 East 23rd Street, Room 6140N, New York, NY 10010. Phone: 212-951-3418; Fax: 212-951-6341; E-mail: peng.lee{at}med.nyu.edu.

Key Words: androgen receptor • LNCaP • LNCaP-AI • prostate cancer growth and invasion

A major obstacle in treating prostate cancer is the development of androgen-independent disease. In this study, we examined LEF1 expression in androgen-independent cancer as well as its regulation of androgen receptor (AR) expression, prostate cancer growth, and invasion in androgen-independent prostate cancer cells. Affymetrix microarray analysis of LNCaP and LNCaP-AI (androgen-independent variant LNCaP) cells revealed 100-fold increases in LEF1 expression in LNCaP-AI cells. We showed that LEF1 overexpression in LNCaP cells resulted in increased AR expression and consequently enhanced growth and invasion ability, whereas LEF1 knockdown in LNCaP-AI cells decreased AR expression and, subsequently, growth and invasion capacity. Chromatin immunoprecipitation, gel shift, and luciferase assays confirmed LEF1 occupancy and regulation of the AR promoter. Thus, we identified LEF1 as a potential marker for androgen-independent disease and as a key regulator of AR expression and prostate cancer growth and invasion. LEF1 is highly expressed in androgen-independent prostate cancer, potentially serving as a marker for androgen-independent disease. [Cancer Res 2009;69(8):3332–8]