Osman Iman, Yee Herman, Taneja Samir S, Levinson Benjamin, Zeleniuch-Jacquotte Anne, Chang Caroline, Nobert Craig, Nanus David M
Department of Urology, New York University Cancer Institute, Kaplan Comprehensive Cancer Center, New York, New York, USA.
Clin Cancer Res. 2004 Jun 15;10(12 Pt 1):4096-100. doi: 10.1158/1078-0432.CCR-04-0120.
Neutral endopeptidase (NEP) is a cell-surface peptidase that inactivates neuropeptide growth factors implicated in prostate cancer progression. The clinical significance of decreased NEP expression observed in prostate cancer is unclear. We investigated whether decreased NEP expression in localized prostate cancers is associated with prostate-specific antigen (PSA) relapse after radical prostatectomy.
NEP expression patterns were examined by immunohistochemistry in 223 men, who underwent radical prostatectomy between 1990 and 2000 at the Veterans Administration Medical Center (New York, NY) with available representative tissues and adequate follow up. We also examined whether hypermethylation of the NEP promoter contributes to down-regulation of NEP protein expression in a subset of patients that showed decreased NEP expression (n = 22).
Three patterns of NEP expression were observed: (a) membranous expression similar to benign prostate epithelium (n = 82; 37%); (b) complete loss of NEP expression in prostate cancer compared with adjacent benign prostate glands (n = 105; 47%); and (c) heterogeneous NEP expression (n = 36; 16%). In a multivariate analysis, complete loss of NEP expression was associated with PSA relapse after controlling for grade, stage, pretreatment PSA, and race simultaneously (hazard ratio, 1.99; 95% confidence interval, 1.13-3.52; two-sided chi(2) P = 0.017). In addition, DNA hypermethylation of the NEP promoter was frequently (73%) identified in a subset of 22 of cases that showed decreased NEP expression.
Our data suggest that decreased NEP expression might contribute to progression of localized prostate cancer after surgery. Data also suggest that methylation is an important mechanism of NEP protein silencing. Larger prospective studies are required for confirmation.
中性内肽酶(NEP)是一种细胞表面肽酶,可使与前列腺癌进展相关的神经肽生长因子失活。在前列腺癌中观察到的NEP表达降低的临床意义尚不清楚。我们研究了局限性前列腺癌中NEP表达降低是否与根治性前列腺切除术后前列腺特异性抗原(PSA)复发相关。
通过免疫组织化学检查了223名男性的NEP表达模式,这些男性于1990年至2000年在退伍军人管理局医疗中心(纽约,纽约)接受了根治性前列腺切除术,有可用的代表性组织并进行了充分的随访。我们还检查了NEP启动子的高甲基化是否导致一部分NEP表达降低的患者(n = 22)中NEP蛋白表达的下调。
观察到三种NEP表达模式:(a)与良性前列腺上皮相似的膜性表达(n = 82; 37%);(b)与相邻良性前列腺腺相比,前列腺癌中NEP表达完全丧失(n = 105; 47%);(c)异质性NEP表达(n = 36; 16%)。在多变量分析中,在同时控制分级、分期、治疗前PSA和种族后,NEP表达完全丧失与PSA复发相关(风险比,1.99; 95%置信区间,1.13 - 3.52;双侧chi(2) P = 0.017)。此外,在显示NEP表达降低的22例病例的子集中,经常(73%)发现NEP启动子的DNA高甲基化。
我们的数据表明,NEP表达降低可能有助于术后局限性前列腺癌的进展。数据还表明甲基化是NEP蛋白沉默的重要机制。需要更大规模的前瞻性研究来证实。