Membrane-type matrix metalloproteinase-1(MT1-MMP) gene is overexpressed in highly invasive hepatocellular carcinomas

被引:67
作者
Harada, T
Arii, S
Mise, M
Imamura, T
Higashitsuji, H
Furutani, M
Niwano, M
Ishigami, S
Fukumoto, M
Seiki, M
Sato, H
Imamura, M
机构
[1] Kyoto Univ, Fac Med, Dept Surg 1, Sakyo Ku, Kyoto 60601, Japan
[2] Kyoto Univ, Fac Med, Dept Pathol 1, Sakyo Ku, Kyoto 60601, Japan
[3] Kanazawa Univ, Canc Res Inst, Dept Mol Virol & Oncol, Kanazawa, Ishikawa 920, Japan
关键词
hepatocellular carcinoma; immunohistochemistry; in situ hybridization; MT1-MMP; Northern blot;
D O I
10.1016/0168-8278(88)80010-2
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background / Aims: The matrix metalloproteinase (MMP) family play important roles in the invasion of cancer cells by degrading the extracellular matrices, The current study was designed to determine the expression pattern of membrane-type matrix metalloproteinase-1 (MT1-MMP) in hepatocellular carcinomas and its participation in invasion potential. Methods: MT1-MMP mRNA expression was examined in 25 human hepatocellular carcinoma specimens using Northern blot, and the correlation to clinicopathological features was evaluated. In situ hybridization and immunohistochemistry were performed to study the localization and the cells responsible for the production. Results: Northern blot analysis revealed high levels of MT1-MMP mRNA expression in tumorous portions in all cases, whereas in non-tumorous portions moderate or faint expression was evident in 22/25 cases. In 21/25 cases, the expression levels in tumorous portion were higher than those in non-tumorous portion. In particular, hepatocellular carcinoma with capsule infiltration emonstrated significantly higher expression than those without (p<0.05), In situ hybridization and immunohistochemical study revealed MT1-MMP transcripts and proteins in cancer cells and stromal cells, respectively. MT1-MMP positive cells were preferentially observed in the invading border of tumor nests, The MMP-2 transcript showed a similar pattern to that of MT1-MMP by in situ hybridization. Conclusion: The present study showed that the MT1-MMP gene is strongly expressed in hepatocellular carcinoma cells and is involved in the invasion potential of hepatocellular carcinoma, and also that MT1-MMP may be one of the key molecules responsible for the invasion potential of hepatocellular carcinoma. Furthermore, the evidence suggests that MT1-MMP and MMP-2 cooperate in the process of cancer invasion.
引用
收藏
页码:231 / 239
页数:9
相关论文
共 38 条
[1]  
Arii S, 1996, HEPATOLOGY, V24, P316
[2]   ASSOCIATION OF MMP-2 ACTIVATION POTENTIAL WITH METASTATIC PROGRESSION IN HUMAN BREAST-CANCER CELL-LINES INDEPENDENT OF MMP-2 PRODUCTION [J].
AZZAM, HS ;
ARAND, G ;
LIPPMAN, ME ;
THOMPSON, EW .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (21) :1758-1764
[3]   MATRIX METALLOPROTEINASES - A REVIEW [J].
BIRKEDALHANSEN, H ;
MOORE, WGI ;
BODDEN, MK ;
WINDSOR, LJ ;
BIRKEDALHANSEN, B ;
DECARLO, A ;
ENGLER, JA .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 1993, 4 (02) :197-250
[4]   ASSOCIATION BETWEEN EXPRESSION OF ACTIVATED 72-KILODALTON GELATINASE AND TUMOR SPREAD IN NON-SMALL-CELL LUNG-CARCINOMA [J].
BROWN, PD ;
BLOXIDGE, RE ;
STUART, NSA ;
GATTER, KC ;
CARMICHAEL, J .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (07) :574-578
[5]   EXPRESSION OF ACTIVATED GELATINASE IN HUMAN INVASIVE BREAST-CARCINOMA [J].
BROWN, PD ;
BLOXIDGE, RE ;
ANDERSON, E ;
HOWELL, A .
CLINICAL & EXPERIMENTAL METASTASIS, 1993, 11 (02) :183-189
[6]   CELLULAR ACTIVATION OF THE 72 KDA TYPE-IV PROCOLLAGENASE/TIMP-2 COMPLEX [J].
BROWN, PD ;
KLEINER, DE ;
UNSWORTH, EJ ;
STETLERSTEVENSON, WG .
KIDNEY INTERNATIONAL, 1993, 43 (01) :163-170
[7]  
COLLIER IE, 1988, J BIOL CHEM, V263, P6579
[8]   ACTIVITY OF TYPE-IV COLLAGENASES IN BENIGN AND MALIGNANT BREAST DISEASE [J].
DAVIES, B ;
MILES, DW ;
HAPPERFIELD, LC ;
NAYLOR, MS ;
BOBROW, LG ;
RUBENS, RD ;
BALKWILL, FR .
BRITISH JOURNAL OF CANCER, 1993, 67 (05) :1126-1131
[9]  
DAVIES B, 1993, CANCER RES, V53, P5365
[10]  
EDMONDSON HA, 1954, CANCER-AM CANCER SOC, V7, P462, DOI 10.1002/1097-0142(195405)7:3<462::AID-CNCR2820070308>3.0.CO