Prognostic significance of p27 expression in carcinoma of the oral cavity and oropharynx

被引:41
作者
Venkatesan, TK
Kuropkat, C
Caldarelli, DD
Panje, WR
Hutchinson, JC
Chen, SD
Coon, JS
机构
[1] Rush Presbyterian St Lukes Med Ctr, Dept Otolaryngol & Bronchoesophagol, Rush Med Coll, Chicago, IL 60612 USA
[2] Rush Presbyterian St Lukes Med Ctr, Dept Pathol, Rush Med Coll, Chicago, IL 60612 USA
[3] Rush Presbyterian St Lukes Med Ctr, Dept Prevent Med, Rush Med Coll, Chicago, IL 60612 USA
[4] Rush Presbyterian St Lukes Med Ctr, Rush Canc Inst, Rush Med Coll, Chicago, IL 60612 USA
关键词
p27; oral cavity; squamous cell carcinoma; immunohistochemistry;
D O I
10.1097/00005537-199908000-00029
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective: To study the role of p27, a cyclin-dependent kinase inhibitor, as a prognostic indicator in squamous cell carcinoma of the oral cavity and oropharynx, Study Design: Retrospective review of 35 patients with squamous cell carcinoma of the oral cavity and oropharynx who presented to Rush-Presbyterian-St. Luke's Medical Center, Chicago, Illinois, between 1986 and 1995, Methods: Inclusion criteria were the availability of clinical information, archival pretreatment biopsy material, and a minimum follow-up of 24 months. p27 staining was scored for frequency and intensity of tumor cell expression following immunoperoxidase staining using standard techniques. Samples of squamous epithelium from the uvula of 15 nonsmoking patients without past or present squamous cell carcinoma were used as normal controls. Results: The association of p27 staining and other factors with response to treatment was evaluated by Fisher's Exact Test and with overall and disease-free survival by the Kaplan-Meier method with multivariate Cox regression. Low levels of p27 expression correlated significantly with unfavorable treatment response (P < .0001), shorter overall survival (P = .0001), and shorter disease-free survival (P = .003). Tumor site (alveolus) was also associated with shorter disease-free (though not overall) survival, but the association with p27 was independent of stage and site in multivariate analysis.
引用
收藏
页码:1329 / 1333
页数:5
相关论文
共 14 条
[1]   Regulation of the cyclin-dependent kinase inhibitor p27 by degradation and phosphorylation [J].
Alessandrini, A ;
Chiaur, DS ;
Pagano, M .
LEUKEMIA, 1997, 11 (03) :342-345
[2]  
[Anonymous], CANC HEAD NECK
[3]   Decreased levels of the cell-cycle inhibitor p27(Kip1) protein: Prognostic implications in primary breast cancer [J].
Catzavelos, C ;
Bhatacharya, N ;
Ung, YC ;
Wilson, JA ;
Roncari, L ;
Sandhu, C ;
Shaw, P ;
Yeger, H ;
MoravaProtzner, I ;
Kapusta, L ;
Franssen, E ;
Pritchard, KI ;
Slingerland, JM .
NATURE MEDICINE, 1997, 3 (02) :227-230
[4]   A syndrome of multiorgan hyperplasia with features of gigantism, tumorigenesis, and female sterility in p27(Kip1)-deficient mice [J].
Fero, ML ;
Rivkin, M ;
Tasch, M ;
Porter, P ;
Carow, CE ;
Firpo, E ;
Polyak, K ;
Tsai, LH ;
Broudy, V ;
Perlmutter, RM ;
Kaushansky, K ;
Roberts, JM .
CELL, 1996, 85 (05) :733-744
[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]  
Jordan RCK, 1998, AM J PATHOL, V152, P585
[7]  
Katayose Y, 1997, CANCER RES, V57, P5441
[8]  
KAWAMATA N, 1995, CANCER RES, V55, P2266
[9]   Enhanced growth of mice lacking the cyclin-dependent kinase inhibitor function of p27(Kip1) [J].
Kiyokawa, H ;
Kineman, RD ;
ManovaTodorova, KO ;
Soares, VC ;
Hoffman, ES ;
Ono, M ;
Khanam, D ;
Hayday, AC ;
Frohman, LA ;
Koff, A .
CELL, 1996, 85 (05) :721-732
[10]   Mice lacking p27(Kip1) display increased body size, multiple organ hyperplasia, retinal dysplasia, and pituitary tumors [J].
Nakayama, K ;
Ishida, N ;
Shirane, M ;
Inomata, A ;
Inoue, T ;
Shishido, N ;
Hori, I ;
Loh, DY ;
Nakayama, K .
CELL, 1996, 85 (05) :707-720