Department of Urology, Eberhard Karls University, Tuebingen, Hoppe-Seyler-Str. 3, 72076 Tuebingen, Germany.
Anticancer Res. 2011 Nov;31(11):3783-8.
To investigate the protein kinase B (Akt) signalling proteins phosphatase and tensin homolog (PTEN), phosphorylated-Akt (p-Akt) and cyclin-dependent kinase inhibitor 1B (p27(Kip1)) in non-seminomatous germ cell tumors (NST) with a view to future investigative approaches.
The expressions of PTEN, p-Akt and p27(Kip1) were immunohistochemically assessed in 17 teratomas, 27 embryonal cell carcinomas, 6 yolk sac tumors and 24 benign testicular parenchymas. The cytoplasmic and corresponding nuclear expressions were compared and correlated to tumor entity.
PTEN was dramatically reduced in all the NST subgroups. Concentrated nuclear p27(Kip1) and loss of the cytoplasmic form was found in teratomas and embryonal cell carcinomas. Neither altered expression nor negative Akt regulation was found. The yolk sac tumors showed late cytoplasmic shift of PTEN and p27(Kip1).
Both, the absence of overexpression of p-Akt and of negative correlations to PTEN and p27(Kip1) suggest that signalling of these parameters in NST might include additional mechanisms such as crosstalk to other pathways rather than classical Akt activation.
研究非精原细胞瘤生殖细胞肿瘤(NST)中的蛋白激酶 B(Akt)信号蛋白磷酸酶和张力蛋白同源物(PTEN)、磷酸化-Akt(p-Akt)和细胞周期蛋白依赖性激酶抑制剂 1B(p27(Kip1)),以期未来的研究方法。
采用免疫组织化学方法检测 17 例畸胎瘤、27 例胚胎性癌、6 例卵黄囊瘤和 24 例良性睾丸实质中 PTEN、p-Akt 和 p27(Kip1)的表达。比较细胞质和相应核的表达,并与肿瘤实体相关联。
所有 NST 亚组中 PTEN 均明显减少。在畸胎瘤和胚胎性癌中发现浓缩的核 p27(Kip1)和细胞质形式的丢失。既没有改变的表达,也没有 Akt 调节的负性。卵黄囊瘤显示出 PTEN 和 p27(Kip1)的晚期细胞质移位。
p-Akt 的过度表达不存在,与 PTEN 和 p27(Kip1)也没有负相关关系,这表明这些参数在 NST 中的信号转导可能包括其他机制,如与其他途径的串扰,而不是经典的 Akt 激活。