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J Korean Assoc Maxillofac Plast Reconstr Surg. 2010 Mar;32(2):118-125. Korean. Original Article.
Park YW , Oh YJ , Lee HS .
Department of Oral & Maxillofacial Surgery, College of Dentistry, Gangneung-Wonju National University, Korea. ywpark@gwnu.ac.kr
Department of Oral Anatomy, College of Dentistry, Gangneung-Wonju National University, Korea.
Abstract

BACKGROUND AND PURPOSE: Bone metastases rarely occur in patients with oral squamous cell carcinoma (OSCC), so the molecular mechanisms of bone metastasis of OSCC remains unclear. Studies with animal models allow progresses in understanding the molecular events for bone metastasis and provide new targets for therapy. So we tried to establish a murine model for bone metastasis of oral squamous cell carcinoma. MATERIALS AND METHODS: Human OSCC cells (KB cell line) were xenografted to nude mice via direct inoculation into the tibial marrow. Mice with tibial tumors were sacrificed once a week, until seven weeks after the injection of human tumor cells. Growth of tibial tumors were observed by histology. Expression of TGF-beta and CXCR-4 in bone OSCC (experimental) and subcutaneous tumor (control) was also evaluated by immunohistochemical staining. RESULTS: Bone OSCC was successfully induced by intra-tibial injection of KB cells. Tumor mass was developed in the marrow tissues of tibia and finally invade the endosteum of tibia. Immunohistochemical staining showed higher expression of TGF-beta in bone tumors than in subcutaneous tumors. CONCLUSION: A murine model of bone metastasis of OSCC was suggested that imitated the clinical findings of distant vascular metastasis. This bone tumor model should facilitate understanding of the molecular pathogenesis of OSCC bone metastasis, and aid in the developement of treatment strategies against OSCC bone metastasis.

Copyright © 2019. Korean Association of Medical Journal Editors.