Matrix metalloproteinase-2 and-9 in bile as a marker of liver metastasis in colorectal cancer

被引:55
作者
Okada, N
Ishida, H
Murata, N
Hashimoto, D
Seyama, Y
Kubota, S
机构
[1] Univ Tokyo, Grad Sch Med, Dept Physiol Chem & Metab, Bunkyo Ku, Tokyo 1130033, Japan
[2] Saitama Med Sch, Saitama Med Ctr, Dept Surg, Kawagoe, Saitama 3508550, Japan
关键词
MMP-2; MMP-9; bile; metastasis; colorectal cancer;
D O I
10.1006/bbrc.2001.5741
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Matrix metallproteinases (MMP)-2 and -9 are associated with cancer invasion and metastasis. MMP-2 and MMP-9 activities have never been assayed in bile. In the present study we investigated whether MMP-2 and -9 activities in the bile could be a marker for evaluation of liver metastasis in colorectal cancer. Fifty-three patients underwent colorectal resection for histologically verified adenocarcinoma. Twenty-six patients had colorectal cancer without liver metastasis and 27 patients had metastatic liver tumor. Six patients were studied as carcinoma-free control. MMP-2 and MMP-9 activities were assayed in bile using gelatin zymography and quantitated. Active MMP-2 activity of colorectal cancer with liver metastasis group (24.1 +/- 2.5 pixel count) was significantly higher than that of colorectal cancer without liver metastasis group (11.4 +/- 1.3 pixel count) (P < 0.001) or of control group (6.4 +/- 1.0 pixel count) (P < 0.0010). Active MMP-9 was not detected in bile. ProMMP-9 activity of colorectal cancer with liver metastasis group (530.3 +/- 127.5 pixel count) was significantly higher than that of colorectal cancer without liver metastasis group (213.9 +/- 33.2 pixel count) (P = 0.008). This is the first report showing that the levels of active MMP-2 and proMMP-9 in bile were significantly higher in liver metastasis of colorectal cancer than in metastasis-free colorectal cancer. The results suggest that activities of active MMP-2 and proMMP-9 in the bile may be useful markers for predicting liver metastasis in colorectal cancer. (C) 2001 Academic Press.
引用
收藏
页码:212 / 216
页数:5
相关论文
共 30 条
[1]   Matrix metalloproteinases, their tissue inhibitors and colorectal cancer staging [J].
Baker, EA ;
Bergin, FG ;
Leaper, DJ .
BRITISH JOURNAL OF SURGERY, 2000, 87 (09) :1215-1221
[2]   Matrix metalloproteinases: molecular aspects of their roles in tumour invasion and metastasis [J].
Curran, S ;
Murray, GI .
EUROPEAN JOURNAL OF CANCER, 2000, 36 (13) :1621-1630
[3]  
Endo K, 1997, ANTICANCER RES, V17, P2253
[4]   Proteolysis in colorectal cancer [J].
Garbett, EA ;
Reed, MWR ;
Brown, NJ .
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY, 1999, 52 (03) :140-145
[5]   ELECTROPHORETIC ANALYSIS OF PLASMINOGEN ACTIVATORS IN POLYACRYLAMIDE GELS CONTAINING SODIUM DODECYL-SULFATE AND COPOLYMERIZED SUBSTRATES [J].
HEUSSEN, C ;
DOWDLE, EB .
ANALYTICAL BIOCHEMISTRY, 1980, 102 (01) :196-202
[6]   Significance of coexpression of urokinase-type plasminogen activator, and matrix metalloproteinase 3 (stromelysin) and 9 (gelatinase B) in colorectal carcinoma [J].
Inuzuka, K ;
Ogata, Y ;
Nagase, H ;
Shirouzu, K .
JOURNAL OF SURGICAL RESEARCH, 2000, 93 (02) :211-218
[7]  
Karakiulakis George, 1997, Invasion and Metastasis, V17, P158
[8]   QUANTITATIVE ZYMOGRAPHY - DETECTION OF PICOGRAM QUANTITIES OF GELATINASES [J].
KLEINER, DE ;
STETLERSTEVENSON, WG .
ANALYTICAL BIOCHEMISTRY, 1994, 218 (02) :325-329
[9]   Ornithine decarboxylase overexpression in mouse 10T1/2 fibroblasts: Cellular transformation and invasion [J].
Kubota, S ;
Kiyosawa, H ;
Nomura, Y ;
Yamada, T ;
Seyama, Y .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (08) :567-571
[10]  
Kubota S, 1997, INT J CANCER, V70, P106