High expression of osteoglycin decreases gelatinase activity of murine hepatocarcinoma Hca-F cells

被引:10
作者
Cui, Xiao-Nan [2 ]
Tang, Jian-Wu [1 ]
Song, Bo [1 ]
Wang, Bo [1 ]
Chen, Shan-Yan [3 ]
Hou, Li [1 ]
机构
[1] Dalian Med Univ, Dept Pathol, Dalian 116044, Liaoning, Peoples R China
[2] Dalian Med Univ, Dept Oncol, Affiliated Hosp 1, Dalian 116011, Liaoning, Peoples R China
[3] Huazhong Univ Sci & Technol, Tongji Med Coll, Wuhan 430074, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Osteoglycin; Transfection; Hepatocellular carcinoma; Neoplasm metastasis; Genes; Gelatinases; NECROSIS-FACTOR-ALPHA; MATRIX METALLOPROTEINASES; EXTRACELLULAR-MATRIX; INVASIVE ABILITY; BOVINE MIMECAN; DEFICIENT MICE; BREAST-CANCER; METASTASIS; GROWTH; MICROENVIRONMENT;
D O I
10.3748/wjg.15.6117
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate the possible correlation between osteoglycin expression and gelatinase activity of mouse hepatocarcinoma Hca-F cells. METHODS: A eukaryotic expression plasmid pIRESpuro3 osteoglycin(+) was constructed and transfected into Hca-F cells to investigate the possible correlation between osteoglycin expression and gelatinase activity of Hca-F cells cultured with extract of lymph node, liver, spleen or in DMEM medium. The activity of gelatinases was examined through zymographic analysis. RESULTS: High expression of osteoglycin attenuated the gelatinase activity of Hca-F cells cultured with extract of lymph node, and at the same time, decreased the metastatic potential of Hca-F cells to peripheral lymph nodes in vivo. CONCLUSION: High expression of osteoglycin decreases the gelatinase activity of Hca-F cells cultured with extract of lymph node; regulation of gelatinase activity might be one of mechanisms that osteoglycin contributes to lymphatic metastasis suppression. (C) 2009 The WJG Press and Baishideng. All rights reserved
引用
收藏
页码:6117 / 6122
页数:6
相关论文
共 32 条
[11]   A switch from E-cadherin to N-cadherin expression indicates epithelial to mesenchymal transition and is of strong and independent importance for the progress of prostate cancer [J].
Gravdal, Karsten ;
Halvorsen, Ole J. ;
Haukaas, Svein A. ;
Akslen, Lars A. .
CLINICAL CANCER RESEARCH, 2007, 13 (23) :7003-7011
[12]   Matrix metalloproteinase-9 expression in the normal mucosa-adenoma-dysplasia-adenocarcinoma sequence of the colon [J].
Herszenyi, Laszlo ;
Sipos, Ferenc ;
Galamb, Orsolya ;
Solymosi, Norbert ;
Hritz, Istvan ;
Miheller, Pal ;
Berczi, Lajos ;
Molnar, Bela ;
Tulassay, Zsolt .
PATHOLOGY & ONCOLOGY RESEARCH, 2008, 14 (01) :31-37
[13]   Proteoglycans of the extracellular matrix and growth control [J].
Kresse, H ;
Schönherr, E .
JOURNAL OF CELLULAR PHYSIOLOGY, 2001, 189 (03) :266-274
[14]   The tumor microenvironment and metastatic disease [J].
Lunt, Sarah Jane ;
Chaudary, Naz ;
Hill, Richard P. .
CLINICAL & EXPERIMENTAL METASTASIS, 2009, 26 (01) :19-34
[15]   Cell adhesion molecules, the extracellular matrix and oral squamous carcinoma [J].
Lyons, A. J. ;
Jones, J. .
INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2007, 36 (08) :671-679
[16]   Growth factor binding to the pericellular matrix and its importance in tissue engineering [J].
Macri, Lauren ;
Silverstein, David ;
Clark, Richard A. F. .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (13) :1366-1381
[17]  
Matsunaga Yoshiko, 2004, Research Communications in Molecular Pathology and Pharmacology, V115, P143
[18]   Altered fine structures of corneal and skeletal keratan sulfate and chondroitin/dermatan sulfate in macular corneal dystrophy [J].
Plaas, AH ;
West, LA ;
Thonar, EJA ;
Karcioglu, ZA ;
Smith, CJ ;
Klintworth, GK ;
Hascall, VC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (43) :39788-39796
[19]   Macrophages define the invasive microenvironment in breast cancer [J].
Pollard, Jeffrey W. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2008, 84 (03) :623-630
[20]  
RIES C, 1994, BLOOD, V83, P3638