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抗血管生成剂SU6668抑制异种移植A-431细胞的肿瘤生长。

Antiangiogenic agent SU6668 suppresses the tumor growth of xenografted A-431 cells.

作者信息

Nakamura Takeshi, Ozawa Soji, Kitagawa Yuko, Ueda Masakazu, Kubota Tetsuro, Kitajima Masaki

机构信息

Department of Surgery, School of Medicine, Keio University, Tokyo, Japan.

出版信息

Oncol Rep. 2006 Jan;15(1):79-83.

Abstract

SU6668 is an antiangiogenic agent that acts as a tyrosine kinase inhibitor for the vascular endothelial growth factor (VEGF) receptor. We treated xenografted A-431, a human squamous cell carcinoma cell line, with SU6668 to investigate the efficacy of tumor dormant therapy using angiogenesis inhibitors for patients with squamous cell carcinoma. A-431 cells were transplanted into severe combined immunodeficient (SCID) mice. The treatment group was given SU6668 at a dose of 200 mg/kg orally twice a day for 3 weeks; the control group was given only the vehicle in the same manner and intervals. SU6668 suppressed tumor growth of A-431 cells in the xenograft model. Furthermore, tumor volume and the number of vessels were significantly reduced in the treatment group compared with those of the control. No significant differences in body weight were found between the treatment and control groups, and no toxic reactions occurred during the experiment. We concluded that this agent was safe, efficient and potentially useful for the treatment of patients with squamous cell carcinoma.

摘要

SU6668是一种抗血管生成剂,可作为血管内皮生长因子(VEGF)受体的酪氨酸激酶抑制剂。我们用SU6668处理人鳞状细胞癌细胞系异种移植的A-431,以研究使用血管生成抑制剂对鳞状细胞癌患者进行肿瘤休眠治疗的疗效。将A-431细胞移植到严重联合免疫缺陷(SCID)小鼠体内。治疗组每天口服两次剂量为200mg/kg的SU6668,持续3周;对照组以相同方式和间隔仅给予赋形剂。在异种移植模型中,SU6668抑制了A-431细胞的肿瘤生长。此外,与对照组相比,治疗组的肿瘤体积和血管数量显著减少。治疗组和对照组之间的体重没有显著差异,并且在实验过程中未发生毒性反应。我们得出结论,该药物对鳞状细胞癌患者的治疗是安全、有效的,并且具有潜在的应用价值。

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