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LEF1 in androgen-independent prostate cancer: regulation of androgen receptor expression, prostate cancer growth, and invasion.

机译:LEF1在雄激素非依赖性前列腺癌中:调节雄激素受体表达,前列腺癌生长和侵袭。

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摘要

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.
机译:治疗前列腺癌的主要障碍是雄激素非依赖性疾病的发展。在这项研究中,我们检查了LEF1在雄激素非依赖性癌症中的表达及其对雄激素受体(AR)表达,前列腺癌生长以及在非雄激素非依赖性前列腺癌细胞中的侵袭的调节。 LNCaP和LNCaP-AI(雄激素非依赖性变体LNCaP)细胞的Affymetrix微阵列分析显示LNCaP-AI细胞中LEF1表达增加了100倍。我们显示,LNCaP细胞中的LEF1过表达导致AR表达增加,从而增强了生长和侵袭能力,而LNCaP-AI细胞中的LEF1敲低降低了AR表达,进而降低了生长和侵袭能力。染色质的免疫沉淀,凝胶迁移和荧光素酶测定证实LEF1占用和AR启动子的调节。因此,我们确定LEF1是雄激素非依赖性疾病的潜在标志物,并且是AR表达和前列腺癌生长与侵袭的关键调节剂。 LEF1在不依赖雄激素的前列腺癌中高表达,可能作为不依赖雄激素的疾病的标志物。

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