mdm-2 expression in human testicular germ-cell tumors and its clinical value

Citation
H. Eid et al., mdm-2 expression in human testicular germ-cell tumors and its clinical value, ANTICANC R, 19(4C), 1999, pp. 3485-3490
Citations number
25
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
ISSN journal
02507005 → ACNP
Volume
19
Issue
4C
Year of publication
1999
Pages
3485 - 3490
Database
ISI
SICI code
0250-7005(199907/08)19:4C<3485:MEIHTG>2.0.ZU;2-E
Abstract
Background. In germ cell testicular tumors (GCTT) mdm-2 gene was analyzed f or amplification and transcripts but not for protein. The purpose of this s tudy is to determine whether mdm-2 protein level is aberrant in GCTT and if so, what is the relationship between mdm-2 overexpression and other diseas e parameters including histologic subtypes, p53 status, metastatic potentia l and clinical stage. Methods. 81 testicular germ-cell tumors were screened for their mdm-2 expression at the protein levels using immunohistochemistr y (IHC) and Western blot (WB) analysis. Results. Of 81 GCTTs 45 (55.55%) sh owed mdm-2 nuclear immunoreactivity, 34 (41,97%) of which were strongly pos itive. The incidence of mdm-2 immunostaining was significantly higher (P=0. 0007) in non-seminomas (NSGCT) than in seminomas (SGCT). The frequency of p ositive tumor was higher in tumors from metastatic patients than in tumors from metastatic-free patients (P=0.011). mdm-2 expression was detected sign ificantly more frequently in tumors of advanced stages, i.e. IIB, IIC and I II versus tumors of early stages (I and II/A) (P=0.0098). A significant dif ference between the three stages of disease as to the expression of mdm-2 ( chi(2)=0.0386) could be established, namely the incidence of mdm-2 expressi on increased with an increase in stage. Using Western blotting 22 (68.75%) out of 32 tumors overexpressed the mdm-2 oncoprotein of 90 kd (p90). Conclu sions. mdm-2 expression as detected by immunohistochemistry may provide a r eliable prognostic tool to isolate subgroups of patients with more aggressi ve GCTT.