High prognostic significance of Mdm2/p53 co-overexpression in soft tissue sarcomas of the extremities

被引:66
作者
Würl, P
Meye, A
Schmidt, H
Lautenschläger, C
Kalthoff, H
Rath, FW
Taubert, H [1 ]
机构
[1] Univ Halle Wittenberg, Clin Gen Surg, D-4010 Halle, Germany
[2] Univ Halle Wittenberg, Inst Pathol, D-4010 Halle, Germany
[3] Univ Halle Wittenberg, Inst Med Biometry & Informat, D-4010 Halle, Germany
[4] Univ Kiel, Clin Gen Surg, Kiel, Germany
关键词
soft tissue sarcoma; Mdm2; p53; immunohistochemistry; multivariate prognostic analysis;
D O I
10.1038/sj.onc.1201646
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Soft tissue sarcomas are a heterogenous group of neoplasms with various histological subtypes, Up to now, no individual causal molecular markers; for prognosis and therapeutic success have been identified, A tumorigenic connection between the oncogene product Mdm2 and tumor suppressor p53 is generally accepted, but their possible clinical relevance has not yet been investigated sufficiently in soft tissue sarcoma, In 86 primary soft tissue sarcoma of the extremities (RO-resected, T1/2 N0 M0), Mdm2 and p53 overexpression were investigated by immunohistochemistry. The results were adjusted to clinico-pathological characteristics and evaluated for their prognostic relevance by multivariate analysis, In Cox's multivariate analysis with stratification of Mdm2 to p53 results, we determined four groups which had different prognostic values for relapse-free and overall survival (Mdm2-/p53-<Mdm2-/p53+<Mdm2+/p53-<Mdm2+/p53+). The most striking finding was a relative risk (rr) for overall survival of 18.77 (P=0.006) for patients with Mdm2/p53 co-overexpression (n=40). It is noticeably higher than the additive risk from both factors. Coincident Mdm2/p53 overexpression is an independent molecular marker with the highest prognostic relevance described for soft tissue sarcoma, Thus, a high risk sarcoma group has been defined which we believe requires alternative therapeutic approaches.
引用
收藏
页码:1183 / 1185
页数:3
相关论文
共 18 条
[1]  
Chen JD, 1996, MOL CELL BIOL, V16, P2445
[2]  
CORDONCARDO C, 1994, CANCER RES, V54, P794
[3]   MDM2 GENE AMPLIFICATION AND TRANSCRIPT LEVELS IN HUMAN SARCOMAS - RELATIONSHIP TO TP53 GENE STATUS [J].
FLORENES, VA ;
MAELANDSMO, GM ;
FORUS, A ;
ANDREASSEN, A ;
MYKLEBOST, O ;
FODSTAD, O .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (17) :1297-1302
[4]   Mdm2 promotes the rapid degradation of p53 [J].
Haupt, Y ;
Maya, R ;
Kazaz, A ;
Oren, M .
NATURE, 1997, 387 (6630) :296-299
[5]   Cell type-specific inhibition of p53-mediated apoptosis by mdm2 [J].
Haupt, Y ;
Barak, Y ;
Oren, M .
EMBO JOURNAL, 1996, 15 (07) :1596-1606
[6]   Specific cleavage of the retinoblastoma protein by an ICE-like protease in apoptosis [J].
Janicke, RU ;
Walker, PA ;
Lin, XY ;
Porter, AG .
EMBO JOURNAL, 1996, 15 (24) :6969-6978
[7]   Regulation of p53 stability by Mdm2 [J].
Kubbutat, MHG ;
Jones, SN ;
Vousden, KH .
NATURE, 1997, 387 (6630) :299-303
[8]   Structure of the MDM2 oncoprotein bound to the p53 tumor suppressor transactivation domain [J].
Kussie, PH ;
Gorina, S ;
Marechal, V ;
Elenbaas, B ;
Moreau, J ;
Levine, AJ ;
Pavletich, NP .
SCIENCE, 1996, 274 (5289) :948-953
[9]  
LEACH FS, 1993, CANCER RES, V53, P2231
[10]  
LIN J, 1995, COLD SPRING HARB SYM, V49, P215