CHARACTERISTICS OF INDUCTION OF p27Kip1 AND INVASION INHIBITORY EFFECT OF CEPHARANTHINE ON A HUMAN ORAL SQUAMOUS CELL CARCINOMA CELL LINE

  • HARADA Koji
    Second Department of Oral and Maxillofacial Surgery, University of Tokushima School of Dentistry
  • BANDO Takashi
    Second Department of Oral and Maxillofacial Surgery, University of Tokushima School of Dentistry
  • YOSHIDA Hideo
    Second Department of Oral and Maxillofacial Surgery, University of Tokushima School of Dentistry
  • SATO Mitsunobu
    Second Department of Oral and Maxillofacial Surgery, University of Tokushima School of Dentistry

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  • ヒト口腔へん平上皮癌細胞に対するセファランチンのp27`Kip1´発現誘導と浸潤抑制効果の解析

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Abstract

Cepharanthine is a biscoclaurine alkaloid extracted from Stephania cepharantha Hayata, and has been widely used for the treatment of alopecia areata and leukopenia during radiation therapy, and can exert antitumor effects on several human cancer cells. In this study, we examined the mechanism of invasion inhibitory effects by cepharanthine on a human oral squamous cell carcinoma (SCC) cell line (B88). Treatment of B88 cells with cepharanthine (10-20μg/ml) resulted in significant suppression of cell growth. Moreover, induction of p27Kip1 protein and reduction of cyclin E, Skp2 and c-Myc, were detected by Western blotting. In addition, induction of p27Kip1 mRNA was observed in cepharanthine-treated B88 cells by real-time RT-PCR. Furthermore, cepharanthine markedly inhibited the migration of B88 cells in a Boyden chamber, and out-growth of them. Interestingly, we detected up-regulation of E-cadherin, integrin α5 and maspin, and down-regulation of Tiaml (tumor invasive and metastasis 1) and MTA1 in cepharanthine-treated B88 cells by Western blotting. These results indicate that cepharanthine may inhibit the invasion of a human oral SCC cell through the pathway of p27Kip1 induction.

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