Expression of ADAM-9 mRNA and protein in human breast cancer

被引:119
作者
O'Shea, C
McKie, N
Buggy, Y
Duggan, C
Hill, AD
McDermott, E
O'Higgins, N
Duffy, MJ [1 ]
机构
[1] St Vincents Univ Hosp, Dept Nucl Med, Dublin 4, Ireland
[2] Univ Coll Dublin, Conway Inst Biomol & Biomed Sci, Dublin 2, Ireland
[3] Univ Newcastle, Dept Rheumatol, Newcastle Upon Tyne, Tyne & Wear, England
[4] Univ Coll Dublin, Dept Surg, Dublin 2, Ireland
[5] Imperial Canc Res Fund, Dept Math Stat & Epidmeiol, London, England
关键词
breast cancer; ADAMs; ADAM-9; HER-2/neu; metastasis;
D O I
10.1002/ijc.11161
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The ADAMs (a disintegrin and metalloprotease) are membrane proteins containing both protease and adhesion domains and thus may be potentially important in cancer invasion and metastasis. The aim of our study was to investigate the distribution and potential clinical significance of ADAM-9 in breast cancer. ADAM-9 expression was measured using both reverse transcriptase-polymerase chain reaction (RTPCR) and Western blotting. ADAM-9 mRNA was expressed more frequently in both breast carcinomas (72/110, 66%) and fibroadenomas (21/38, SS%) compared, to normal breast tissue (6125, 24%) (p = 0.0004, p = 0.028, respectively). Multiple forms of ADAM-9 protein were detected by Western blotting, i.e., at 124, 84 and 48 kDa under reducing conditions and at I IS, 76, 55, 52 and 46 kDa under nonreducing conditions. The 84 and 55 kDa forms were detected more frequently in the primary cancers compared to normal breast tissue (p < 0.0001, p = 0.0002, respectively). In addition, relative levels of the 84 kDa mature form were significantly higher in, the primary cancers than in the fibroadenomas (p = 0.003), while the reverse was found for the 124 kDa precursor form (p = 0.026). In the carcinomas, the 84 kDa form of ADAM-9 protein was expressed at higher levels in node-positive than node-negative cancers (p = 0.05) and correlated positively with HER-2/neu protein levels (r = 0.313, p = 0.0 16). This is the first report to describe expression of any ADAM in a large number of human carcinomas. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:754 / 761
页数:8
相关论文
共 51 条
[1]  
ALLEN RW, 1987, J BIOL CHEM, V262, P649
[2]  
Andreasen PA, 1997, INT J CANCER, V72, P1, DOI 10.1002/(SICI)1097-0215(19970703)72:1<1::AID-IJC1>3.0.CO
[3]  
2-Z
[4]   E-cadherin is a tumour invasion suppressor gene mutated in human lobular breast cancers [J].
Berx, G ;
CletonJansen, AM ;
Nollet, F ;
deLeeuw, WJF ;
vandeVijver, MJ ;
Cornelisse, C ;
vanRoy, F .
EMBO JOURNAL, 1995, 14 (24) :6107-6115
[5]   ADAMs: focus on the protease domain [J].
Black, RA ;
White, JM .
CURRENT OPINION IN CELL BIOLOGY, 1998, 10 (05) :654-659
[6]  
Chenard MP, 1996, INT J CANCER, V69, P448, DOI 10.1002/(SICI)1097-0215(19961220)69:6<448::AID-IJC5>3.0.CO
[7]  
2-4
[8]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[9]  
CROFFORD LJ, 1993, J IMMUNOL, V151, P1587
[10]   ASSAY OF MATRIX METALLOPROTEASES TYPE-8 AND TYPE-9 BY ELISA IN HUMAN BREAST-CANCER [J].
DUFFY, MJ ;
BLASER, J ;
DUGGAN, C ;
MCDERMOTT, E ;
OHIGGINS, N ;
FENNELLY, JJ ;
TSCHESCHE, H .
BRITISH JOURNAL OF CANCER, 1995, 71 (05) :1025-1028