Difference in gene expression for matrix metalloproteinase-1 between early and advanced hepatocellular carcinomas

被引:40
作者
Okazaki, I
Wada, N
Nakano, M
Saito, A
Takasaki, K
Doi, M
Kameyama, K
Otani, Y
Kubochi, K
Niioka, M
Watanabe, T
Maruyama, K
机构
[1] CHIBA UNIV HOSP,DEPT PATHOL,CHIBA,JAPAN
[2] TOKYO WOMENS MED COLL,INST GASTROENTEROL,SHINJUKU KU,TOKYO 162,JAPAN
[3] TSUKUBA MED CTR HOSP,DEPT PATHOL,TSUKUBA,IBARAKI,JAPAN
[4] KEIO UNIV,SCH MED,DEPT PATHOL,SHINJUKU KU,TOKYO 160,JAPAN
[5] KEIO UNIV,SCH MED,DEPT SURG,SHINJUKU KU,TOKYO 160,JAPAN
[6] KURIHAMA NATL HOSP,CLIN RES UNIT,NATL INST ALCOHOLISM,YOKOSUKA,KANAGAWA,JAPAN
关键词
D O I
10.1002/hep.510250315
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The histological observation that well-differentiated cancer cells in early hepatocellular carcinoma (HCC) invade portal tracts and/or fibrous bands and that these fibrous tissues then disappear suggests the participation of matrix metalloproteinase-1 (MMP-1) in the degradation of fibrous tissue. To confirm this hypothesis, the authors investigated the localization of both the MMP-1 protein and its messenger RNA (mRNA) in early HCC immunohistochemically and by in situ hybridization using complementary DNA (cDNA) and synthetic antisense probe of MMP-1; they then compared the results with those in advanced HCC. MMP-1 gene transcripts and protein were observed in well-differentiated cancer cells of early HCC but not in moderately or poorly differentiated cancer cells. Thus, cancer cells producing MMP-1 in early HCC may destroy the portal tract tissue adjacent to the cancer lesion and/or the fibrous band of cirrhosis. These results seem to have demonstrated a difference in the mechanism of cancer growth and invasion between early and advanced HCCs.
引用
收藏
页码:580 / 584
页数:5
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