Expression of extracellular matrix metalloproteinase inducer and enhancement of the production of matrix metalloproteinase-1 in tongue squamous cell carcinoma

被引:15
作者
Cao, Z. [2 ]
Xiang, J. [2 ]
Li, C. [1 ,2 ]
机构
[1] Wuhan Univ, Sch Stomatol, Dept Periodontol, Key Lab Oral Biomed Engn,Minist Educ, Wuhan 430079, Peoples R China
[2] Wuhan Univ, Hosp Stomatol, Wuhan 430079, Peoples R China
基金
中国国家自然科学基金;
关键词
squamous cell carcinoma; extracellular matrix metalloproteinase inducer; matrix metalloproteinase-1; SINGLE NUCLEOTIDE POLYMORPHISM; PROMOTER; INVASION; EMMPRIN; DEGRADATION; EFFECTORS; GENES; HEAD; ECM;
D O I
10.1016/j.ijom.2009.03.004
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Recent Studies have found that ill addition to promoting Cellular invasion, overexpression of metalloproteinase-1 (MMP-1) is associated with the initial stages of cancer development. Extracellular matrix metalloproteinase inducer (EMMPRIN), a transmembrane glycoprotein, has been reported to be highly expressed in tumor cells and induce production of MMPs front peritumor fibroblasts (PTFs) adjacent to the tumor cells. The expression or EMMPRIN in tongue squamous Cell carcinoma (SCC) was investigated in this study. It was found that EMMPRIN was expressed at the cell membrane throughout the entire lesion ill tongue SCC. Immunofluorescence staining localized EMMPRIN to the cell membrane in a highly invasive tongue SCC cell line (Tca 8113). EMMPRIN mRNA was expressed at a high level in Tca 8113, whereas MMP-1 mRNA was expressed ill PTF but harder to be detected in Tca 8113. Co-culture of Tea 8113 with PTF stimulated production of MMP-1. EMMPRIN was highly expressed in tongue SCC, and could induce local production of MMP-1. These data indicate that EMMPRIN might play an important role in tongue SCC progression and invasion.
引用
收藏
页码:880 / 885
页数:6
相关论文
共 34 条
[1]   Matrix metalloproteinases as stromal effectors of human carcinoma progression: Therapeutic implications [J].
Basset, P ;
Okada, A ;
Chenard, MP ;
Kannan, R ;
Stoll, I ;
Anglard, P ;
Bellocq, JP ;
Rio, MC .
MATRIX BIOLOGY, 1997, 15 (8-9) :535-541
[2]  
BISWAS C, 1995, CANCER RES, V55, P434
[3]  
Bordador LC, 2000, INT J CANCER, V85, P347, DOI 10.1002/(SICI)1097-0215(20000201)85:3<347::AID-IJC9>3.3.CO
[4]  
2-R
[5]  
Cao ZG, 2006, ORAL ONCOL, V42, P32, DOI [10.1016/j.oraloncology.2004.08.015, 10.1016/j.ooe.2005.08.006]
[6]  
ERIC EG, 2005, BIOCHIMIE, V87, P361
[7]  
GUO G, 1996, J BIOL CHEM, V272, P24
[8]   Association of functional polymorphisms of matrix metalloproteinase (MMP)-1 and MMP-3 genes with colorectal cancer [J].
Hinoda, Y ;
Okayama, N ;
Takano, N ;
Fujimura, K ;
Suehiro, Y ;
Hamanaka, Y ;
Hazama, S ;
Kitamura, Y ;
Kamatani, N ;
Oka, M .
INTERNATIONAL JOURNAL OF CANCER, 2002, 102 (05) :526-529
[9]   Mutations in the SMAD4/DPC4 gene in juvenile polyposis [J].
Howe, JR ;
Roth, S ;
Ringold, JC ;
Summers, RW ;
Järvinen, HJ ;
Sistonen, P ;
Tomlinson, IPM ;
Houlston, RS ;
Bevan, S ;
Mitros, FA ;
Stone, EM ;
Aaltonen, LA .
SCIENCE, 1998, 280 (5366) :1086-1088
[10]  
Hsieh CJ, 1998, CANCER RES, V58, P3942