THE RILE OF TUMOR-DERIVED IL-6 IN MANDIBULAR BONE INVASION OF ORAL CANCER
THE RILE OF TUMOR-DERIVED IL-6 IN MANDIBULAR BONE INVASION OF ORAL CANCER
批准号:
10671886
负责人:
OKAMOTO Masato
金额:
$2.05万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 1999
中文摘要
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英文摘要
BACKGROUND. Osteoclastic bone resorption is an important step in bone invasion in several malignancies. Although IL-6 accelerates osteoclastic bone resorption, it remains unclear whether IL-6 may be involved in bone invasion of oral cancer.METHODS. The pit-formation assay with calf femur-derived bone slices was performed to examine the bone-resorbing activity of osteoclasts and cancer cells. The chemotaxis activity of the culture media were analyzed by the use of Boyden chamber technique. Nude mice which were inoculated IL-6-producing oral cancer cells into masseter, were treated with anti-IL-6 neutralizing antibody, and mandibular bone invasion of the cells were assessed.RESULTS. BHY, a bone invasive oral cancer cell line, but not HNT, a non-invasive cell line, produced large amounts of IL-6. In a pit-formation asssay, addition of conditioned medium (CM) derived from BHY but not HNT increased osteoclastic bone resorption and the effects were inhibited by anti-IL-6 antibody. BHY-secreted IL-6 showed significant chemotaxis activity for osteoclasts. Interestingly, CM from the cocultivation of osteoclasts and BHY markedly enhanced the cancer cell migration, and the chemotaxis activity were significantly reduced when anti-IL-6 antibody was added into the coculture then CM were collected, but not when the antibody was added into the CM after they were collected. Futhermore, treatment with anti-IL-6 antibody almost completely inhibited mandibular bone invasion of BHY in nude mice.CONCLUSIONS. These results strongly suggest that IL-6 secreted by oral cancer cells plays a significant role in bone invasion.
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OKAMOTO,M.,et.al.: "Mechanism for bone invasion of Oral Cancer Cells mediated by Interleukin-6 in vitro and in vivo."Cancer. (in press). (2000)
OKAMOTO,M.,et.al.:“体外和体内白细胞介素 6 介导的口腔癌细胞骨侵袭机制。”癌症。
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Okamoto M, Hattori K. Fuiimoto K. Tanaka Y, Gloosby CL, and Oyasu R.: "Antisense RNA- mediated reduction of p5 3 induced malignant phenotype in nontumorigenic rat urothelial cells."Carcinogenesis. 19(1). 73-79 (1998)
Okamoto M、Hattori K. Fuiimoto K. Tanaka Y、Gloosby CL 和 Oyasu R.:“反义 RNA 介导的非致瘤性大鼠尿路上皮细胞中 p5 3 诱导的恶性表型的减少”。致癌作用。
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OKAMOTO,M.,et.al.: "Cis-diammindichloroplatinum and 5-Fluorouracil are potent inducers of the cytokines and natural killer cell activity in vivo and in vitro."Cancer Immunul.Immunother.. 47. 233-241 (1998)
OKAMOTO,M.,et.al.:“顺式二氨二氯铂和 5-氟尿嘧啶是体内和体外细胞因子和自然杀伤细胞活性的有效诱导剂。”Cancer Immunul.Immunother.. 47. 233-241 (1998)
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OKAMOTO M.,et al.: "Cytokine-inducing activity and anti-tumor eddect of liposome-incorprated interferon-γ-inducing moleculeclesiced from OK-432"J.Immunother.. (in press). (2000)
OKAMOTO M.等人:“脂质体掺入的干扰素-γ-诱导分子的细胞因子诱导活性和抗肿瘤效果”,J.Immunother..(2000 年出版)。
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