Nuclear localization of the metastasis-related protein S100A4 correlates with tumour stage in colorectal cancer

被引:73
作者
Flatmark, K
Pedersen, KB
Nesland, JM
Rasmussen, H
Aamodt, G
Mikalsen, SO
Bjornland, K
Fodstad, O
Mælandsmo, GMM [1 ]
机构
[1] Norwegian Radium Hosp, Dept Tumor Biol, N-0310 Oslo, Norway
[2] Norwegian Radium Hosp, Canc Res Inst, N-0310 Oslo, Norway
[3] Norwegian Radium Hosp, Dept Pathol, N-0310 Oslo, Norway
[4] Natl Hosp Norway, Biostat Sect, N-0027 Oslo, Norway
[5] Norwegian Radium Hosp, Dept Environm & Occupat Canc, N-0310 Oslo, Norway
[6] Natl Hosp Norway, Dept Surg, N-0027 Oslo, Norway
[7] Natl Hosp Norway, Inst Surg Res, N-0027 Oslo, Norway
关键词
S100A4; colorectal cancer; metastasis; clinical study; immunohistochemistry;
D O I
10.1002/path.1381
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A large number of experimental studies have linked the S100A4 gene product to the metastatic phenotype of cancer cells and clinical evidence indicates a correlation between S100A4 expression and poor prognosis in several cancer types. The aim of the present study was to analyse the expression of the S100A4 protein in colorectal cancer. Paraffin-embedded samples from 277 colorectal cancer patients were immunostained with anfi-S100A4 antibody. Cytoplasmic staining was observed in 178 of 277 samples (64%), whereas, unexpectedly, nuclear expression of S100A4 was found in 88 of 277 of the samples (32%). This novel finding was confirmed by western blot analysis of nuclear fractions isolated from frozen tumour tissue. Statistical analysis revealed a significant correlation between nuclear expression of S100A4 and tumour stage at diagnosis, while there was no such correlation between cytoplasmic staining and tumour stage. The nuclear localization of S100A4 in colorectal cancer and its relationship to tumour stage suggest that this protein may be involved in gene regulatory pathways of relevance to the metastatic phenotype of cancer cells. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:589 / 595
页数:7
相关论文
共 37 条
[1]   The metastasis-associated Mts1(S100A4) protein could act as an angiogenic factor [J].
Ambartsumian, N ;
Klingelhöfer, J ;
Grigorian, M ;
Christensen, C ;
Kriajevska, M ;
Tulchinsky, E ;
Georgiev, G ;
Berezin, V ;
Bock, E ;
Rygaard, J ;
Cao, RH ;
Cao, YH ;
Lukanidin, E .
ONCOGENE, 2001, 20 (34) :4685-4695
[2]  
Ambartsumian NS, 1996, ONCOGENE, V13, P1621
[3]   INTERACTIONS OF MYOGENIC BHLH TRANSCRIPTION FACTORS WITH CALCIUM-BINDING CALMODULIN AND S100A (ALPHA-ALPHA) PROTEINS [J].
BAUDIER, J ;
BERGERET, E ;
BERTACCHI, N ;
WEINTRAUB, H ;
GAGNON, J ;
GARIN, J .
BIOCHEMISTRY, 1995, 34 (24) :7834-7846
[4]   NUCLEI FROM RAT LIVER - ISOLATION METHOD THAT COMBINES PURITY WITH HIGH YIELD [J].
BLOBEL, G ;
POTTER, VR .
SCIENCE, 1966, 154 (3757) :1662-&
[5]   DREAM is a Ca2+-regulated transcriptional repressor [J].
Carrión, AM ;
Link, WA ;
Ledo, F ;
Mellström, B ;
Naranjo, JR .
NATURE, 1999, 398 (6722) :80-84
[6]   Binding to intracellular targets of the metastasis-inducing protein, S100A4 (p9Ka) [J].
Chen, HL ;
Fernig, DG ;
Rudland, PS ;
Sparks, A ;
Wilkinson, MC ;
Barraclough, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 286 (05) :1212-1217
[7]   Calcium-dependent translocation of S100A11 requires tubulin filaments [J].
Davey, GE ;
Murmann, P ;
Hoechli, M ;
Tanaka, T ;
Heizmann, CW .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2000, 1498 (2-3) :220-232
[8]  
DAVIES BR, 1993, ONCOGENE, V8, P999
[9]   Expression of S100A4 protein is associated with metastasis and reduced survival in human bladder cancer [J].
Davies, BR ;
O'Donnell, M ;
Durkan, GC ;
Rudland, PS ;
Barraclough, R ;
Neal, DE ;
Mellon, JK .
JOURNAL OF PATHOLOGY, 2002, 196 (03) :292-299
[10]  
Davies MPA, 1996, ONCOGENE, V13, P1631