Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.
Hum Pathol. 2010 Feb;41(2):214-22. doi: 10.1016/j.humpath.2009.07.011. Epub 2009 Oct 1.
N-myc downstream regulated gene-1 (NDRG1)/Cap43 plays an important role in tumor progression and metastases in many kinds of cancers. Recently, it was reported that NDRG1/Cap43 is involved in the aggressiveness of prostate cancer and also that its expression is associated with the expression of E-cadherin in prostate carcinoma cell lines. In the current study, to elucidate the functional and pathologic roles of NDRG1/Cap43 in prostate cancer, we investigated whether the expression of NDRG1/Cap43 is associated with the clinicopathologic parameters of prostate cancer or E-cadherin expression. NDRG1/Cap43 expression and E-cadherin expression were examined immunohistochemically in 148 patients with prostate cancer. We investigated the correlation between membranous or cytoplasmic expression of NDRG1/Cap43 and E-cadherin and evaluated the prognostic or clinicopathologic significance of the expression of NDRG1/Cap43. The patients with decreased NDRG1/Cap43 membranous expression showed significantly lower disease-free survival rates compared with the patients with preserved NDRG1/Cap43 membranous expression. Decreased membranous and high cytoplasmic NDRG1/Cap43 expression was also correlated with a higher Gleason score. A significant correlation was observed between NDRG1/Cap43 membranous expression and E-cadherin membranous expression (r = 0.7130; P < .0001) and between NDRG1/Cap43 cytoplasmic expression and E-cadherin cytoplasmic expression (r = 0.5847; P < .0001). Decreased NDRG1/Cap43 membranous expression had a significant impact on patient disease-free survival in multivariate analysis (P = .0175). NDRG1/Cap43 could be a novel marker for malignant progression and poor prognosis in prostate cancer, plausibly in its close association with the down-regulation of E-cadherin expression.
N- MYC 下游调节基因 1(NDRG1)/Cap43 在许多类型的癌症中肿瘤进展和转移中起着重要作用。最近,据报道 NDRG1/Cap43 参与前列腺癌的侵袭性,并且其表达与前列腺癌细胞系中 E-钙粘蛋白的表达相关。在目前的研究中,为了阐明 NDRG1/Cap43 在前列腺癌中的功能和病理作用,我们研究了 NDRG1/Cap43 的表达是否与前列腺癌的临床病理参数或 E-钙粘蛋白表达相关。通过免疫组织化学方法检测了 148 例前列腺癌患者中 NDRG1/Cap43 的表达和 E-钙粘蛋白的表达。我们研究了 NDRG1/Cap43 的膜或细胞质表达与 E-钙粘蛋白之间的相关性,并评估了 NDRG1/Cap43 表达的预后或临床病理意义。与保留 NDRG1/Cap43 膜表达的患者相比,NDRG1/Cap43 膜表达减少的患者显示出明显较低的无病生存率。降低的膜和高细胞质 NDRG1/Cap43 表达也与较高的 Gleason 评分相关。NDRG1/Cap43 膜表达与 E-钙粘蛋白膜表达之间存在显著相关性(r = 0.7130;P <.0001),NDRG1/Cap43 细胞质表达与 E-钙粘蛋白细胞质表达之间也存在显著相关性(r = 0.5847;P <.0001)。在多变量分析中,NDRG1/Cap43 膜表达减少对患者无病生存率有显著影响(P =.0175)。NDRG1/Cap43 可能是前列腺癌恶性进展和不良预后的新标志物,可能与其下调 E-钙粘蛋白表达密切相关。