P53 EXPRESSION IN HEPATOCELLULAR-CARCINOMA IN A POPULATION IN SINGAPORE WITH ENDEMIC HEPATITIS-B VIRUS-INFECTION

被引:10
作者
WEE, A
TEH, M
RAJU, GC
机构
[1] Department of Pathology, National University Hospital, Singapore 0511, Lower Kent Ridge Road
关键词
HEPATOCELLULAR CARCINOMA; IMMUNOHISTOCHEMISTRY; P53; PROTEIN;
D O I
10.1136/jcp.48.3.236
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Aims-To study the expression and clinical significance (if any) of p53 protein in hepatocellular carcinomas (HCC) arising in a population with endemic hepatitis B virus (HBV) infection. Methods-Immunohistochemical staining was performed on formalin fixed, paraffin wax embedded histological sections of 46 HCC cases using an antihuman p53 monoclonal antibody; serial sections were also stained for hepatitis B surface antigen (HBsAg), hepatitis B core antigen (HBcAg) and alpha fetoprotein (AFP). Nuclear p53 staining was assessed according to intensity (absent, weak or strong) and extent (<5%, 6-25%, 26-50%, and >50%) of positive cells. Tissue HBsAg, HBcAg and AFP were recorded as absent or present. Results-The p53 protein was expressed in 35% (16 of 46) of HCCs; the positive rate in grade III/IV tumours (13 of 31; 42%) was higher than in grade I/II tumours (three of 15; 20%) but this was not statistically significant. HBsAg positive tumours showed almost the same proportion of p53 staining (11 of 29; 38%) as HBsAg negative ones (five of 17; 29%). Conclusions-The p53 protein was expressed in 35% of HCC cases. There was no statistically significant correlation between HBV infection and p53 protein expression. Similarly, there was no definite correlation between p53 positivity and tumour size, histological grade or vascular invasion.
引用
收藏
页码:236 / 238
页数:3
相关论文
共 26 条
[1]   SELECTIVE G-MUTATION TO T-MUTATION OF P53 GENE IN HEPATOCELLULAR-CARCINOMA FROM SOUTHERN AFRICA [J].
BRESSAC, B ;
KEW, M ;
WANDS, J ;
OZTURK, M .
NATURE, 1991, 350 (6317) :429-431
[2]   ANALYSIS OF THE P53 TUMOR-SUPPRESSOR GENE IN HEPATOCELLULAR CARCINOMAS FROM BRITAIN [J].
CHALLEN, C ;
LUNEC, J ;
WARREN, W ;
COLLIER, J ;
BASSENDINE, MF .
HEPATOLOGY, 1992, 16 (06) :1362-1366
[3]  
CHALLEN C, 1991, HEPATOLOGY, V14, pA94
[4]   EXPRESSION OF MUTANT P53 PROTEIN IN HEPATOCELLULAR-CARCINOMA [J].
COLLIER, JD ;
CARPENTER, M ;
BURT, AD ;
BASSENDINE, MF .
GUT, 1994, 35 (01) :98-100
[5]  
EDMONDSON HA, 1954, CANCER-AM CANCER SOC, V7, P462, DOI 10.1002/1097-0142(195405)7:3<462::AID-CNCR2820070308>3.0.CO
[6]  
2-E
[7]   OVERPRODUCTION OF P53 ANTIGEN MAKES ESTABLISHED CELLS HIGHLY TUMORIGENIC [J].
ELIYAHU, D ;
MICHALOVITZ, D ;
OREN, M .
NATURE, 1985, 316 (6024) :158-160
[8]   THE P53 PROTO-ONCOGENE CAN ACT AS A SUPPRESSOR OF TRANSFORMATION [J].
FINLAY, CA ;
HINDS, PW ;
LEVINE, AJ .
CELL, 1989, 57 (07) :1083-1093
[9]   P53 IN TUMOR PATHOLOGY - CAN WE TRUST IMMUNOHISTOCHEMISTRY - REVISITED [J].
HALL, PA ;
LANE, DP .
JOURNAL OF PATHOLOGY, 1994, 172 (01) :1-4
[10]  
HAN KA, 1992, CANCER RES, V52, P749