β-catenin accumulation and mutation of exon 3 of the β-catenin gene in hepatocellular carcinoma

被引:85
作者
Kondo, Y
Kanai, Y
Sakamoto, M
Genda, T
Mizokami, M
Ueda, R
Hirohashi, S
机构
[1] Natl Canc Ctr, Res Inst, Div Pathol, Chuo Ku, Tokyo 1040045, Japan
[2] Nagoya City Univ, Dept Med 2, Mizuho Ku, Nagoya, Aichi 4678601, Japan
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 1999年 / 90卷 / 12期
关键词
hepatocellular carcinoma; beta-catenin; single strand conformation polymorphism;
D O I
10.1111/j.1349-7006.1999.tb00712.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A study was conducted to clarify the contribution of beta-catenin accumulation and mutation of the beta-catenin gene to hepatocarcinogenesis. beta-Catenin accumulation was examined immunohistochemically in 38 paired samples of hepatocellular carcinoma (HCC) and corresponding non-cancerous liver tissue. Gene mutation was analyzed by polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) and direct sequencing using intronic primers encompassing exon 3, Neither accumulation nor mutation was detected in non-cancerous liver tissues that showed no remarkable histological features, chronic hepatitis or liver cirrhosis, Accumulation of beta-catenin was seen in the nucleus, cytoplasm or cell membrane in 15 of 38 (39%) HCC samples, and gene mutation was seen in 9 of 38 (24%) HCC samples. Although there was a significant correlation between accumulation and mutation (P<0.01), six HCCs without mutation also showed accumulation, Samples of early HCC show ed neither accumulation nor mutation, and accumulation and mutation were each correlated significantly with portal vein tumor involvement (P<0.05). The present results indicate that (1) mutation of exon 3 of the beta-catenin gene can lead to beta-catenin accumulation, although other mechanisms of accumulation may also operate in HCC, and (2) beta-catenin accumulation and mutation of the beta-catenin gene are not early events in hepatocarcinogenesis, and may be associated with the malignant progression of HCC.
引用
收藏
页码:1301 / 1309
页数:9
相关论文
共 28 条
[1]  
[Anonymous], 1989, MOL CLONING LAB MANU
[2]   Functional interaction of an axin homolog, conductin, with β-catenin, APC, and GSK3β [J].
Behrens, J ;
Jerchow, BA ;
Würtele, M ;
Grimm, J ;
Asbrand, C ;
Wirtz, R ;
Kühl, M ;
Wedlich, D ;
Birchmeier, W .
SCIENCE, 1998, 280 (5363) :596-599
[3]   Functional interaction of beta-catenin with the transcription factor LEF-1 [J].
Behrens, J ;
vonKries, JP ;
Kuhl, M ;
Bruhn, L ;
Wedlich, D ;
Grosschedl, R ;
Birchmeier, W .
NATURE, 1996, 382 (6592) :638-642
[4]   Absence of APC gene mutation in the mutation cluster region in hepatocellular carcinoma [J].
Chen, TC ;
Hsieh, LL ;
Ng, KF ;
Jeng, LB ;
Chen, MF .
CANCER LETTERS, 1998, 134 (01) :23-28
[5]  
de La Coste A, 1998, P NATL ACAD SCI USA, V95, P8847
[6]  
EDMONDSON HA, 1954, CANCER-AM CANCER SOC, V7, P462, DOI 10.1002/1097-0142(195405)7:3<462::AID-CNCR2820070308>3.0.CO
[7]  
2-E
[8]   Laser capture microdissection [J].
EmmertBuck, MR ;
Bonner, RF ;
Smith, PD ;
Chuaqui, RF ;
Zhuang, ZP ;
Goldstein, SR ;
Weiss, RA ;
Liotta, LA .
SCIENCE, 1996, 274 (5289) :998-1001
[9]  
Fukuchi T, 1998, CANCER RES, V58, P3526
[10]   EMBRYONIC AXIS INDUCTION BY THE ARMADILLO REPEAT DOMAIN OF BETA-CATENIN - EVIDENCE FOR INTRACELLULAR SIGNALING [J].
FUNAYAMA, N ;
FAGOTTO, F ;
MCCREA, P ;
GUMBINER, BM .
JOURNAL OF CELL BIOLOGY, 1995, 128 (05) :959-968