Weikert Steffen, Schrader Mark, Krause Hans, Schulze Wolfgang, Müller Markus, Miller Kurt
Department of Urology, Charité, University Medicine in Berlin, Joint Faculty of Medicine of the Free University Berlin and Humboldt University Berlin, Campus Benjamin Franklin, Hindenburgdamm 30 D-12200 Berlin, Germany.
Cancer Lett. 2005 Jun 8;223(2):331-7. doi: 10.1016/j.canlet.2004.10.038. Epub 2004 Dec 8.
Deregulated apoptosis of germ cells may contribute to malignant transformation as well as male infertility. We analyzed expression of the inhibitor of apoptosis survivin by polymerase chain reaction (PCR) in testicular germ cell tumors (TGCTs, n=28), normal testes (n=19) and testes with defective spermatogenesis (n=22). In a subset of samples (n=35), survivin transcript levels were quantified using real-time PCR. While survivin mRNA was expressed at high levels in undifferentiated TGCTs and normal testes, it was lost in mature teratomas and germ cell aplasia. Survivin expression in both normal and transformed germ cells is in contrast to its sharp differential expression in other tissues. Survivin expression correlates with the differentiation state of TGCTs and may be relevant for their tumorigenesis and malignant potential.
生殖细胞凋亡失调可能导致恶性转化以及男性不育。我们通过聚合酶链反应(PCR)分析了睾丸生殖细胞肿瘤(TGCT,n = 28)、正常睾丸(n = 19)和生精功能缺陷的睾丸(n = 22)中凋亡抑制因子survivin的表达。在一部分样本(n = 35)中,使用实时PCR对survivin转录水平进行了定量。虽然survivin mRNA在未分化的TGCT和正常睾丸中高水平表达,但在成熟畸胎瘤和生殖细胞发育不全中则缺失。Survivin在正常和转化的生殖细胞中的表达与其在其他组织中的明显差异表达形成对比。Survivin表达与TGCT的分化状态相关,可能与其肿瘤发生和恶性潜能有关。