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口服新型丝氨酸蛋白酶抑制剂ONO-3403对小鼠自发性皮肤癌的生长抑制作用

Growth inhibition of mouse autochthonous skin cancer by oral administration of new serine protease inhibitor ONO-3403.

作者信息

Ohkoshi Motohiro, Okuda Satoru

机构信息

Department of Oral and Maxillo-Facial Surgery, Branch Hospital, Faculty of Medicine, The University of Tokyo, Japan.

出版信息

Anticancer Res. 2002 Mar-Apr;22(2A):821-3.

Abstract

The orally active serine protease inhibitor ONO-3403 is an analog of FOY-3403 that has more potent protease-inhibitory activity. In the present study, oral administration of ONO-3403 was used to challenge 3-methylcholanthrene-induced carcinoma. This drug was administered 3 times daily for 9 weeks via a stomach tube at a dose of 10 mg/kg in a 1-ml volume in 6 mice harboring solid tumors. This protease inhibitor significantly inhibited tumor growth (p<0.001) and prolonged survival-time (p<0.01). These results indicated that oral administration of the potent serine protease inhibitor ONO-3403 has an antitumor effect on malignant tumors.

摘要

口服活性丝氨酸蛋白酶抑制剂ONO - 3403是具有更强蛋白酶抑制活性的FOY - 3403类似物。在本研究中,采用口服ONO - 3403对3 - 甲基胆蒽诱导的癌进行挑战。通过胃管以10mg/kg的剂量、1ml的体积,对6只患有实体瘤的小鼠每日给药3次,持续9周。这种蛋白酶抑制剂显著抑制了肿瘤生长(p<0.001)并延长了生存时间(p<0.01)。这些结果表明,口服强效丝氨酸蛋白酶抑制剂ONO - 3403对恶性肿瘤具有抗肿瘤作用。

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