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Clinical Cancer Research Vol. 11, 8458-8466, December 1, 2005
© 2005 American Association for Cancer Research


Cancer Therapy: Preclinical

FTY720: A Promising Agent for Treatment of Metastatic Hepatocellular Carcinoma

Terence K. Lee1,2, Kwan Man1,2, Joanna W. Ho1,2, Xiang Hong Wang3, Ronnie T.P. Poon1,2, Yang Xu6, Kevin T. Ng1,2, Alan C. Chu1,2, Chris K. Sun1,2, Irene O. Ng1,4, Hui Chuan Sun6, Zao You Tang6, Ray Xu1,5 and Sheung Tat Fan1,2

Authors' Affiliations: 1 Centre for the Study of Liver Disease; Departments of 2 Surgery, 3 Anatomy, and 4 Pathology; 5 Institute of Molecular Biology, The University of Hong Kong, Pokfulam, Hong Kong, China; and 6 Department of Surgery, Zhongshan Hospital, Fudan University, Shanghai, China

Requests for reprints: Kwan Man, Department of Surgery, The University of Hong Kong, L9-55, Faculty of Medicine Building, 21 Sassoon Road, Hong Kong. Phone: 852-2819-9646; Fax: 852-2819-9634; E-mail: kwanman{at}hkucc.hku.hk.

Purpose: Recurrence after resection and metastasis are common in hepatocellular carcinoma and are associated with poor prognosis. Therefore, effective treatment is urgently needed for improvement of patients' survival. Previously, we reported that FTY720 has an antimetastatic effect on hepatocellular carcinoma cell line through down-regulation of Rac signaling pathway. This study aims to investigate the in vivo antimetastatic potential of FTY720 in an orthotopic nude mice model using metastatic human hepatocellular carcinoma cell lines MHCC-97L (lower metastatic potential) and MHCC-97H (higher metastatic potential).

Experimental Design: The nude mice bearing liver tumors were randomized into a treatment group and a control group, each with 12 mice. FTY720 was administered at a dosage of 5 or 10 mg/kg via i.p. injection after 7 days of tumor inoculation. Thirty-five days later, the mice were sacrificed for record of intrahepatic and pulmonary metastases.

Results: After 35 days of FTY720 treatment at the dosages of 5 and 10 mg/kg, all 12 mice in the treatment group were alive and well. FTY720 at the dosages of 5 and 10 mg/kg significantly suppressed the tumor volume and intrahepatic and pulmonary metastases in the metastatic nude mice model. FTY720 suppressed intrahepatic and pulmonary metastases by inhibition of Rac expression, which at least in part down-regulated the vascular endothelial growth factor expression and CD34 staining in a dose-dependent manner.

Conclusion: FTY720 is a promising novel therapeutic drug for treatment of hepatocellular carcinoma metastasis.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2005 by the American Association for Cancer Research.