Reduced expression of cyclin-dependent kinase inhibitor p27Kip1 in oval malignant tumors

被引:16
作者
Ito, R
Yasui, W
Ogawa, Y
Toyosawa, S
Tahara, E
Ijuhin, N
机构
[1] Osaka Univ, Fac Dent, Dept Oral Pathol, Suita, Osaka 5650871, Japan
[2] Hiroshima Univ, Sch Med, Dept Pathol 1, Hiroshima 734, Japan
关键词
cyclin-dependent kinase inhibitor; p27(Kip1); oral tumors; immunohistochemistry;
D O I
10.1159/000028068
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
p27(Kip1), cyclin-dependent kinase (CDK) inhibitor, blocks progression from the G(1) to S phase by binding cyclin E-CDK2 and inhibiting their activities. We studied the expression of p27 in oral tumors by immunohistochemistry to determine whether lack of p27 plays a role in the development and progression of oral cancer. Reduced expression of p27 was detected in 86% of the squamous cell carcinomas and 95% of the mucoepidermoid carcinomas, respectively, while p27 expression was well preserved in the pleomorphic adenomas, The expression of p27 showed an inverse correlation with the expression of cyclin E in the squamous cell carcinomas and mucoepidermoid carcinomas. However, there was no relationship between clinicopathological parameters and p27 expression. These results suggest that the reduction of p27 protein may confer the development of oral squamous cell carcinoma and mucoepidermoid carcinoma partly through the increased expression of cyclin E. Copyright (C) 2000 S. Karger AG, Basel.
引用
收藏
页码:169 / 173
页数:5
相关论文
共 23 条
[1]   Requirement of p27(Kip1) for restriction point control of the fibroblast cell cycle [J].
Coats, S ;
Flanagan, WM ;
Nourse, J ;
Roberts, JM .
SCIENCE, 1996, 272 (5263) :877-880
[2]   MAMMALIAN G(1) CYCLINS [J].
DRAETTA, GF .
CURRENT OPINION IN CELL BIOLOGY, 1994, 6 (06) :842-846
[3]   High level expression of p27(kip1) and cyclin D1 in some human breast cancer cells: Inverse correlation between the expression of p27(kip1) and degree of malignancy in human breast and colorectal cancers [J].
Fredersdorf, S ;
Burns, J ;
Milne, AM ;
Packham, G ;
Fallis, L ;
Gillett, CE ;
Royds, JA ;
Peston, D ;
Hall, PA ;
Hanby, AM ;
Barnes, DM ;
Shousha, S ;
OHare, MJ ;
Lu, X .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (12) :6380-6385
[4]  
HARPER JW, 1993, CELL, V75, P805
[5]   CYCLINS AND CANCER .2. CYCLIN-D AND CDK INHIBITORS COME OF AGE [J].
HUNTER, T ;
PINES, J .
CELL, 1994, 79 (04) :573-582
[6]  
KEYOMARSI K, 1994, CANCER RES, V54, P380
[7]   CONCURRENT AMPLIFICATION OF CYCLIN-E AND CDK2 GENES IN COLORECTAL CARCINOMAS [J].
KITAHARA, K ;
YASUI, W ;
KUNIYASU, H ;
YOKOZAKI, H ;
AKAMA, Y ;
YUNOTANI, S ;
HISATSUGU, T ;
TAHARA, E .
INTERNATIONAL JOURNAL OF CANCER, 1995, 62 (01) :25-28
[8]   Increased proteasome-dependent degradation of the cyclin-dependent kinase inhibitor p27 in aggressive colorectal carcinomas [J].
Loda, M ;
Cukor, B ;
Tam, SW ;
Lavin, P ;
Fiorentino, M ;
Draetta, GF ;
Jessup, JM ;
Pagano, M .
NATURE MEDICINE, 1997, 3 (02) :231-234
[9]   CANCER OF THE UPPER AERODIGESTIVE TRACT - BASIC PRINCIPLES AND CONCEPTS [J].
MCGUIRT, WF .
POSTGRADUATE MEDICINE, 1986, 80 (01) :77-&
[10]  
Michalides RJAM, 1997, ARCH OTOLARYNGOL, V123, P497