Protein expression of MDM2 and its clinicopathological relationships in human hepatocellular carcinoma

被引:47
作者
Endo, K
Ueda, T
Ohta, T
Terada, T
机构
[1] Tottori Univ, Fac Med, Dept Pathol 2, Yonago, Tottori 6838503, Japan
[2] Kanazawa Univ, Sch Med, Dept Surg 2, Kanazawa, Ishikawa 920, Japan
来源
LIVER | 2000年 / 20卷 / 03期
关键词
mdm2; hepatocellular carcinoma; immunohistochemistry; clinicopathologic correlation; survival;
D O I
10.1034/j.1600-0676.2000.020003209.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The transcription of mdm2 gene is activated by p53 and this limits the growth-suppressing activity of p53 by direct binding. It has been reported that MDM2 protein is overexpressed in several types of cancers. Bo However, there have been no immunohistochemical studies on MDM2 in human hepatocellular carcinoma (HCC). Methods. We immunohistochemically examined the expression of MDM2 and the relationships between its expression and histological grade, clinicopathological parameters, p53 expression and patient survival in 107 patients with HCC. Results: The frequency of MDM2 positivity in the nuclei of HCC cells was 28/107 (26%). There was no correlation between the MDM2 expression and HCC grade. However, positivity of MDM2 expression significantly correlated with small HCC size (p<0.05, chi(2) test) and the absence of vascular invasion (p<0.01, chi(2) test). No significant differences were noted between MDM2 expression and capsular invasion or satellite nodules. Expression of MDM2 showed a significantly positive correlation with expression of p53 (p<0.03, chi(2) test). Patients with positive expression of MDM2 had poorer prognosis than patients with negative MDM2 expression. MDM2 expression was the most useful independent factor for overall survival (p=0.0001). Conclusions. MDM2 was expressed in 26% of HCC, and its expression correlated positively with p53 mutations. MDM2 over-expression is a useful predictor of poor prognosis in patients with HCC following hepatic resection.
引用
收藏
页码:209 / 215
页数:7
相关论文
共 56 条
[1]   MDM2 EXPRESSION IS INDUCED BY WILD TYPE-P53 ACTIVITY [J].
BARAK, Y ;
JUVEN, T ;
HAFFNER, R ;
OREN, M .
EMBO JOURNAL, 1993, 12 (02) :461-468
[2]  
Baunoch DA, 1996, INT J ONCOL, V8, P895
[3]  
Casey G, 1996, ONCOGENE, V13, P1971
[4]   INTERACTIONS BETWEEN P53 AND MDM2 IN A MAMMALIAN-CELL CYCLE CHECKPOINT PATHWAY [J].
CHEN, CY ;
OLINER, JD ;
ZHAN, QM ;
FORNACE, AJ ;
VOGELSTEIN, B ;
KASTAN, MB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (07) :2684-2688
[5]   CRYSTAL-STRUCTURE OF A P53 TUMOR-SUPPRESSOR DNA COMPLEX - UNDERSTANDING TUMORIGENIC MUTATIONS [J].
CHO, YJ ;
GORINA, S ;
JEFFREY, PD ;
PAVLETICH, NP .
SCIENCE, 1994, 265 (5170) :346-355
[6]   WAF1, A POTENTIAL MEDIATOR OF P53 TUMOR SUPPRESSION [J].
ELDEIRY, WS ;
TOKINO, T ;
VELCULESCU, VE ;
LEVY, DB ;
PARSONS, R ;
TRENT, JM ;
LIN, D ;
MERCER, WE ;
KINZLER, KW ;
VOGELSTEIN, B .
CELL, 1993, 75 (04) :817-825
[7]   TUMORIGENIC POTENTIAL ASSOCIATED WITH ENHANCED EXPRESSION OF A GENE THAT IS AMPLIFIED IN A MOUSE-TUMOR CELL-LINE [J].
FAKHARZADEH, SS ;
TRUSKO, SP ;
GEORGE, DL .
EMBO JOURNAL, 1991, 10 (06) :1565-1569
[8]  
GUDAS JM, 1995, CLIN CANCER RES, V1, P71
[9]   ONCOGENE AMPLIFICATION IN UROTHELIAL CANCERS WITH P53 GENE MUTATION OR MDM2 AMPLIFICATION [J].
HABUCHI, T ;
KINOSHITA, H ;
YAMADA, H ;
KAKEHI, Y ;
OGAWA, O ;
WU, WJ ;
TAKAHASHI, R ;
SUGIYAMA, T ;
YOSHIDA, O .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (17) :1331-1335
[10]   Mdm2 promotes the rapid degradation of p53 [J].
Haupt, Y ;
Maya, R ;
Kazaz, A ;
Oren, M .
NATURE, 1997, 387 (6630) :296-299