Expression of p53, Ki-67 and cytokeratin-4 (CK4) in oral papillomas

被引:6
作者
Copete, MA
Wendt, K
Chen, SY
机构
[1] TEMPLE UNIV,SCH MED,DEPT PATHOL & LAB MED,ORAL PATHOL SECT,PHILADELPHIA,PA 19140
[2] UNIV SASKATCHEWAN,FAC DENT,SASKATOON,SK,CANADA
关键词
cytokeratin-4; Ki-67; p53; papillomas;
D O I
10.1111/j.1600-0714.1997.tb01226.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
P53 is overexpressed in more than 50% of all human cancers. A previous study suggested that p53 was also overexpressed in oral papillomas. This study was carried out to investigate whether p53 expression was correlated with expression of the cellular proliferation marker Ki-67 and the epithelial differentiation marker cytokeratin-4 (CK4) in oral papillomas. Formalin-fixed paraffin-embedded sections of 30 oral papilloma specimens and 30 unmatched normal oral mucosal specimens were processed for immunohistochemistry, using an avidin-biotin- peroxidase procedure and monoclonal antibodies. A semiquantification analysis on p53 and Ki-67 labeling indices was performed. Twenty-eight of 30 (93%) papilloma specimens were positive for p53. The percentage of p53-positive cells in the basal layer was 60.4+/-14.8 (mean+/-SD, n=28), and that of Ki-67-positive cells was 26.7+/-14.4. There was no correlation between expression of p53 and that of Ki-67. Expression of CK4 was inversely correlated with the expression of Ki-67 but not correlated with the expression of p53.
引用
收藏
页码:211 / 216
页数:6
相关论文
共 39 条
[11]   P53 - AT THE CROSSROADS OF MOLECULAR CARCINOGENESIS AND RISK ASSESSMENT [J].
HARRIS, CC .
SCIENCE, 1993, 262 (5142) :1980-1981
[12]   USE OF AVIDIN-BIOTIN-PEROXIDASE COMPLEX (ABC) IN IMMUNOPEROXIDASE TECHNIQUES - A COMPARISON BETWEEN ABC AND UNLABELED ANTIBODY (PAP) PROCEDURES [J].
HSU, SM ;
RAINE, L ;
FANGER, H .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1981, 29 (04) :577-580
[13]   HUMAN PAPILLOMAVIRUS TYPE-16-E6 INCREASES THE DEGRADATION RATE OF P53 IN HUMAN KERATINOCYTES [J].
HUBBERT, NL ;
SEDMAN, SA ;
SCHILLER, JT .
JOURNAL OF VIROLOGY, 1992, 66 (10) :6237-6241
[14]   E6-AP DIRECTS THE HPV E6-DEPENDENT INACTIVATION OF P53 AND IS REPRESENTATIVE OF A FAMILY OF STRUCTURALLY AND FUNCTIONALLY RELATED PROTEINS [J].
HUIBREGTSE, JM ;
SCHEFFNER, M ;
HOWLEY, PM .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1994, 59 :237-245
[15]   ANALYSIS OF ORAL PAPILLOMAS, LEUKOPLAKIAS, AND INVASIVE CARCINOMAS FOR HUMAN PAPILLOMAVIRUS TYPE RELATED DNA [J].
LONING, T ;
IKENBERG, H ;
BECKER, J ;
GISSMANN, L ;
HOEPFER, I ;
HAUSEN, HZ .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1985, 84 (05) :417-420
[16]   HUMAN PAPILLOMAVIRUS TYPE-16 IN BOWENOID PAPULOSIS, INTRAORAL PAPILLOMAS, AND SQUAMOUS-CELL CARCINOMA OF THE TONGUE [J].
LOOKINGBILL, DP ;
KREIDER, JW ;
HOWETT, MK ;
OLMSTEAD, PM ;
CONNER, GH .
ARCHIVES OF DERMATOLOGY, 1987, 123 (03) :363-368
[17]   DIFFERENT PAPILLOMAVIRUSES AS THE CAUSES OF ORAL WARTS [J].
LUTZNER, M ;
KUFFER, R ;
BLANCHETBARDON, C ;
CROISSANT, O .
ARCHIVES OF DERMATOLOGY, 1982, 118 (06) :393-399
[18]  
MADINIER I, 1987, J BIOL BUCCALE, V15, P105
[19]  
Moll R, 1991, Acta Histochem Suppl, V41, P117
[20]   THE MDM-2 ONCOGENE PRODUCT FORMS A COMPLEX WITH THE P53 PROTEIN AND INHIBITS P53-MEDIATED TRANSACTIVATION [J].
MOMAND, J ;
ZAMBETTI, GP ;
OLSON, DC ;
GEORGE, D ;
LEVINE, AJ .
CELL, 1992, 69 (07) :1237-1245