Expression of Tissue Levels of Matrix Metalloproteinases and Tissue Inhibitors of Metalloproteinases in Gastric Adenocarcinoma

被引:39
|
作者
Zhang, Ming [1 ]
Zhu, Guan-Yu [1 ]
Gao, Hong-Yu [1 ]
Zhao, Shu-Peng [1 ]
Xue, Yingwei [1 ]
机构
[1] Harbin Med Coll, Affiliated Tumor Hosp, Dept Surg Gastroenterol, Harbin 150040, Peoples R China
关键词
gastric cancer; matrix metalloproteinase; semi-quantitative RT-PCR; tissue inhibitor of metalloproteinase; CANCER INVASION; TUMOR INVASION; MESSENGER-RNA; LYMPH-NODE; METASTASIS; CARCINOMAS; PROGRESSION; CELLS; GELATINASES; ACTIVATION;
D O I
10.1002/jso.21824
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and Objectives: Matrix metalloproteinases (MMPs) are one of the major classes of proteolytic enzymes involved in tumor invasion and metastasis, being inhibited by naturally occurring tissue inhibitors of metalloproteinases (TIMPs). We examined mRNA expression for MMP-2, MMP-7, MMP-9, MT1-MMP, TIMP-1, and TIMP-2 in human gastric adenocarcinoma tissues, and the correlation between their expression and clinicopathological variables. Methods: Gastric tissue samples from 72 patients with gastric adenocarcinoma were available for this study. To determine mRNA expression for MMP-2, MMP-7, MMP-9, MT1-MMP, TIMP-1, and TIMP-2, semiquantitative reverse transcriptase-polymerase chain reaction (RT-PCR) was carried out on tumor and normal tissues, respectively. Results: Mean MMP-2, MMP-7, MMP-9, MT1-MMP, TIMP-1, and TIMP-2 m RNA expression in the gastric adenocarcinomas was significantly higher than in the normal tissue. In terms of the invasion of the tumor, lymph node metastasis, and tumor stage of gastric adenocarcinoma, the differences in MMP-2, MMP-7, MMP-9, and MT1-MMP mRNA expression levels were significant. MMP-2, MMP-7, MMP-9, MT1-MMP, TIMP-1, and TIMP-2 mRNA expression did not differ significantly in relation to histological type of gastric adenocarcinoma. Conclusion: The correlation between the increased expression of MMP-2, MMP-7, MMP-9, and MT1-MMP and clinicopathological parameters reflects a role in predicting the aggressive behavior of gastric cancer. J. Surg. Oncol. 2011;103:243-247. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:243 / 247
页数:5
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