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p27(Kip1) 相互作用的细胞周期调节剂在成人睾丸生殖细胞肿瘤中的异常表达:在肿瘤发生和组织学进展中的潜在作用。

Altered expression of p27(Kip1) -interacting cell-cycle regulators in the adult testicular germ cell tumors: potential role in tumor development and histological progression.

机构信息

Department of Basic Pathology, National Defense Medical College, Tokorozawa, Saitama, Japan.

出版信息

APMIS. 2012 Nov;120(11):890-900. doi: 10.1111/j.1600-0463.2012.02919.x. Epub 2012 May 24.

DOI:10.1111/j.1600-0463.2012.02919.x
PMID:23009113
Abstract

We examined the potential role of cell-cycle dysregulation in the development and histological progression of adult testicular germ cell tumors (TGCTs). Expressions of p27(Kip1) -interacting cell-cycle regulators (down-regulation of p27(Kip1) and overexpression of Skp2, Cks1, cyclin A, and cyclin E) and Ki-67 labeling index (LI) were immunohistochemically examined in histological components of 50 intratubular germ cell neoplasms, unclassified (IGCNUs); 74 seminomas; and 25 embryonal carcinomas, identified from 88 patients. Altered expression of p27(Kip1) , Skp2, Cks1, cyclin A, and cyclin E was observed in 20%, 12%, 16%, 10%, and 24% of IGCNUs; 26%, 36%, 27%, 89%, and 23% of seminomas; and 48%, 68%, 56%, 100%, and 60% of embryonal carcinomas, respectively. A significant difference in the frequency of Skp2 and cyclin A overexpression was observed between IGCNUs and seminomas. Significantly more frequent alterations of Skp2, Cks1, and cyclin E and p27(Kip1) were detected in embryonal carcinomas than in seminomas. Alterations of all cell-cycle regulators were significantly more frequent in embryonal carcinomas than in IGCNUs. The mean Ki-67 LI significantly increased from IGCNU (21.2%) through seminoma (34.7%) to embryonal carcinoma (54.2%). These results suggest that alterations of the p27(Kip1) -interacting cell-cycle regulators are common in TGCTs and may be involved in their histological progression.

摘要

我们研究了细胞周期失调在成人睾丸生殖细胞肿瘤(TGCTs)的发展和组织学进展中的潜在作用。在 88 例患者中确定的 50 例管内生殖细胞肿瘤未分类(IGCNUs);74 例精原细胞瘤;和 25 例胚胎癌的组织学成分中,用免疫组织化学方法检查了 p27(Kip1)相互作用的细胞周期调节剂(p27(Kip1)下调和 Skp2、Cks1、细胞周期蛋白 A 和细胞周期蛋白 E 过表达)和 Ki-67 标记指数(LI)的表达。在 IGCNUs 中观察到 p27(Kip1)、Skp2、Cks1、细胞周期蛋白 A 和细胞周期蛋白 E 的表达改变分别为 20%、12%、16%、10%和 24%;精原细胞瘤分别为 26%、36%、27%、89%和 23%;胚胎癌分别为 48%、68%、56%、100%和 60%。IGCNUs 和精原细胞瘤之间 Skp2 和细胞周期蛋白 A 过表达的频率存在显著差异。在胚胎癌中,Skp2、Cks1 和细胞周期蛋白 E 以及 p27(Kip1)的改变更为频繁。与精原细胞瘤相比,胚胎癌中 Skp2、Cks1 和细胞周期蛋白 E 的改变更为频繁。所有细胞周期调节剂的改变在胚胎癌中比在 IGCNUs 中更为频繁。Ki-67 LI 均值从 IGCNU(21.2%)到精原细胞瘤(34.7%)再到胚胎癌(54.2%)显著增加。这些结果表明,p27(Kip1)相互作用的细胞周期调节剂的改变在 TGCTs 中很常见,可能参与其组织学进展。

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