Expression of MIP-3α/CCL20, a macrophage inflammatory protein in oral squamous cell carcinoma

被引:52
作者
Abiko, Y [1 ]
Nishimura, M
Kusano, K
Nakashima, K
Okumura, K
Arakawa, T
Takuma, T
Mizoguchi, I
Kaku, T
机构
[1] Hlth Sci Univ Hokkaido, Sch Dent, Dept Oral Pathol, Ishikari, Hokkaido 0610293, Japan
[2] Hlth Sci Univ Hokkaido, Sch Dent, Dept Periodontol, Ishikari, Hokkaido 0610293, Japan
[3] Hlth Sci Univ Hokkaido, Sch Dent, Dept Oral Maxillofacial Surg, Ishikari, Hokkaido 0610293, Japan
[4] Hlth Sci Univ Hokkaido, Sch Dent, Dept Oral Biochem, Ishikari, Hokkaido 0610293, Japan
[5] Hlth Sci Univ Hokkaido, Sch Dent, Dept Orthodont, Ishikari, Hokkaido 0610293, Japan
关键词
MIP-3; alpha/LARC/EXODUS/CCL20; squamous cell; carcinoma; quantitative; RT-PCR; bacterial infection; cytokine;
D O I
10.1016/S0003-9969(02)00167-X
中图分类号
R78 [口腔科学];
学科分类号
1003 [口腔医学];
摘要
We have examined the expression of MIP-3alpha/CCL20 in oral squamous cell carcinoma (SCC) in vivo and in vitro. In addition, we have investigated whether the expression of MIP-3a/CCL20 is regulated by bacterial. infection and inflammatory cytokines. In order to determine the mRNA level of MIP-3alpha, quantitative reverse transcription-polymerase chain reaction (RT-PCR) was performed with LightCycter(TM) using the double-stranded DNA dye, SYBR Green 1. Oral epithelial. cells and six SCC cell lines (SCC-9, SAS, BSC-OF, HSC-4, HSC, Ca9-22) were found to express MIP-3alpha mRNA. The expression of MIP-3alpha was upregutated by infection with Actinobacillus actinomycetemcomitans and by stimulation with lipopolysaccharide and TNF-alpha. By in situ hybridization, the detectable MIP-3alpha expression in SCC was localized primarily at the epithelial pearls corresponding to the spinous layer. These results suggest that MIP-3alpha contributes to the oral immunoresponse to bacterial infection, and may be involved in the growth of SCC. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:171 / 175
页数:5
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