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Insulin-like growth factor binding protein-6 inhibits prostate cancer cell proliferation: implication for anticancer effect of diethylstilbestrol in hormone refractory prostate cancer

机译:胰岛素样生长因子结合蛋白6抑制前列腺癌细胞增殖:己烯雌酚在激素难治性前列腺癌中的抗癌作用

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摘要

Diethylstilbestrol (DES) is a synthetic oestrogen, and its anticancer effects are exerted in androgen-dependent prostate cancer. The administration of DES decreases serum testosterone to castration levels. However, in androgen-independent prostate cancer patients, who are already orchiectomised, the administration of DES improves symptoms and decreases prostate-specific antigen (PSA). The mechanisms responsible for these direct inhibitory effects have been explained as biological actions not mediated by oestrogen receptors. We assessed the gene expression profiles of prostate cancer cells treated with DES, and investigated direct inhibitory effects of DES. DES inhibited the proliferation of LNCaP and PC-3 cells. cDNA microarray analysis showed that expression of many genes was downregulated by DES. However, insulin-like growth factor binding protein 6 (IGFBP-6) gene expression levels were upregulated in PC-3 cells. IGFBP-6 gene expression and protein levels significantly increased after DES treatment. Recombinant IGFBP-6 inhibited cell proliferation, and the inhibitory effect of DES was neutralised by anti-IGFBP-6 antibody. From the immunohistochemical analysis of IGFBP-6 using biopsy samples from androgen-independent prostate cancer, we found IGFBP-6 expression in androgen independent prostate cancer, and that DES treatment increased the IGFBP-6 staining intensity of the cancer cells in one sample. These findings suggested that DES induces IGFBP-6, which inhibits cell proliferation in an androgen-independent prostate cancer cell line, PC-3. IGFBP-6 therefore might be involved in the direct effects of DES in androgen-independent prostate cancer.
机译:己烯雌酚(DES)是一种合成雌激素,其抗癌作用在雄激素依赖性前列腺癌中发挥作用。 DES的给药将血清睾丸激素降低至去势水平。但是,在已经进行睾丸切除的雄激素非依赖性前列腺癌患者中,DES的使用改善了症状并降低了前列腺特异性抗原(PSA)。造成这些直接抑制作用的机制已被解释为不是由雌激素受体介导的生物学作用。我们评估了用DES处理过的前列腺癌细胞的基因表达谱,并研究了DES的直接抑制作用。 DES抑制LNCaP和PC-3细胞的增殖。 cDNA微阵列分析表明,DES下调了许多基因的表达。但是,胰岛素样生长因子结合蛋白6(IGFBP-6)基因表达水平在PC-3细胞中上调。 DES处理后,IGFBP-6基因表达和蛋白质水平显着增加。重组IGFBP-6抑制细胞增殖,并且抗IGFBP-6抗体中和了DES的抑制作用。使用来自雄激素非依赖性前列腺癌的活检样本对IGFBP-6进行免疫组织化学分析,我们发现IGFBP-6在非雄激素非依赖性前列腺癌中表达,并且DES处理增加了一个样本中癌细胞的IGFBP-6染色强度。这些发现表明,DES诱导IGFBP-6,其抑制雄激素非依赖性前列腺癌细胞系PC-3中的细胞增殖。因此,IGFBP-6可能参与了DES在雄激素非依赖性前列腺癌中的直接作用。

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