P53 BUT NOT ERBB-2 EXPRESSION IS ASSOCIATED WITH RAPID TUMOR PROLIFERATION IN URINARY-BLADDER CANCER

被引:58
作者
MOCH, H
SAUTER, G
MIHATSCH, MJ
GUDAT, F
EPPER, R
WALDMAN, FM
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT LAB MED,DIV MOLEC CYTOMETRY,SAN FRANCISCO,CA 94143
[2] UNIV BASEL,DEPT PATHOL,BASEL,SWITZERLAND
关键词
BLADDER NEOPLASMS; KI67; P53; ERBB-2;
D O I
10.1016/0046-8177(94)90096-5
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Tumor proliferation in bladder cancer is associated with tumor behavior. To assess the association between Ki-67 labeling index (LI), p53, and c-erbB-2 overexpression, formalin-fixed tissue samples of 160 patients with transitional cell carcinoma (TCC) of the urinary bladder were studied by immunohistochemistry. Ki-67 LI was strongly associated with tumor stage (P < .0001), tumor grade (P < .0001), and p53 status (P = .0014) but not with erbB-2 overexpression (P > .2). Ki-67 LT was higher in p53-positive tumors (19%) than in p53-negative tumors (14%) when all stages were compared. Ki-67 LI was independent of p53 expression in pTa tumors (p53-positive, 9%; p53-negative, 11%), showing that p53 overexpression alone is not sufficient to induce rapid tumor cell proliferation in pTa tumors. Ki-67 LI also was independent of p53 expression in pT2 to pT4 tumors (p53-positive, 20%; p53-negative, 23%), indicating that p53 expression is not necessary for rapid tumor cell proliferation in advanced stages. However, there was a striking difference in Ki-67 LI between p53-positive pT1 tumors (22.0% +/- 8.8 standard deviation [SD]; n = 20) and p53-negative pT1 tumors (9.7 +/- 8.3 SD; n = 22; P=.0001). These results suggest that increased proliferation in p53-positive pT1 tumors is caused by additional alterations that occur during tumor progression. Copyright (C) 1994 by W.B. Saunders Company
引用
收藏
页码:1346 / 1351
页数:6
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