Koike H, Ito K, Takezawa Y, Oyama T, Yamanaka H, Suzuki K
Department of Urology, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maeabshi, Gunma 3718511, Japan.
Br J Cancer. 2005 Apr 25;92(8):1538-44. doi: 10.1038/sj.bjc.6602520.
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.
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。给予DES可使血清睾酮降至去势水平。然而,在已经接受睾丸切除术的雄激素非依赖性前列腺癌患者中,给予DES可改善症状并降低前列腺特异性抗原(PSA)。这些直接抑制作用的机制被解释为非由雌激素受体介导的生物学作用。我们评估了用DES处理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,许多基因的表达被DES下调。然而,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基因表达和蛋白水平显著增加。重组IGFBP-6抑制细胞增殖,并且DES的抑制作用被抗IGFBP-6抗体中和。通过对雄激素非依赖性前列腺癌活检样本进行IGFBP-6免疫组织化学分析,我们发现在雄激素非依赖性前列腺癌中有IGFBP-6表达,并且在一个样本中DES处理增加了癌细胞的IGFBP-6染色强度。这些发现表明,DES诱导IGFBP-6,其在雄激素非依赖性前列腺癌细胞系PC-3中抑制细胞增殖。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。