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血管生成抑制剂O-(氯乙酰-氨甲酰基)烟曲霉素(TNP-470;AGM-1470)对啮齿类动物肿瘤生长和转移的抑制作用

Inhibition of tumor growth and metastasis of rodent tumors by the angiogenesis inhibitor O-(chloroacetyl-carbamoyl)fumagillol (TNP-470; AGM-1470).

作者信息

Yamaoka M, Yamamoto T, Masaki T, Ikeyama S, Sudo K, Fujita T

机构信息

Pharmaceutical Research Laboratories III, Takeda Chemical Industries, Ltd., Osaka, Japan.

出版信息

Cancer Res. 1993 Sep 15;53(18):4262-7.

PMID:7689930
Abstract

The effect of the potent angiogenesis inhibitor O-(chloroacetyl-carbamoyl)fumagillol (TNP-470), a semisynthetic analogue of fumagillin, on tumor growth and metastasis was studied using rodent tumors. Injection of TNP-470 s.c. inhibited tumor growth in a dose-dependent manner, and the tumor sizes of B16BL6 melanoma, M5076 reticulum cell sarcoma, Lewis lung carcinoma, and Walker 256 carcinoma were maximally reduced to 16, 10, 17, and 4% of that in the respective control. The activity of TNP-470 upon i.v. injection was slightly weaker than that following s.c. injection. This tendency was observed for all the tumors tested. Injection i.v. (infusion) of TNP-470 increased the life span of Walker 256 carcinoma-bearing rats by 183% over the control, while bolus i.v. injection increased the life span by only 47%. TNP-470 reduced the number of pulmonary metastatic foci of i.v. inoculated B16BL6 melanoma in a dose-dependent manner, and the number of metastatic foci was reduced to 10% of that in the control by treatment with TNP-470 at 60 mg/kg, 3 times/week. The mean survival time of B16BL6 tumor-bearing mice treated with TNP-470 using this regimen was extended by 56% over that of control mice. TNP-470 at 10 mg/kg every day also reduced the number of metastatic foci of M5076 sarcoma in the liver after resection of the tumor from the primary site. Adriamycin at the same dose only slightly reduced the number of metastatic foci, even though TNP-470 and Adriamycin showed roughly equal inhibitory activity against M5076 sarcoma growth. TNP-470 extended the mean survival time of M5076 tumor-bearing mice by more than 100% over that of control mice at 30 mg/kg every 3 days, while Adriamycin extended mean survival times by maximally 20% at 10 mg/kg. These results show that the angiogenesis inhibitor TNP-470 has strong inhibitory activities against in vivo growth and metastasis of a wide variety of tumors.

摘要

使用啮齿动物肿瘤模型研究了强效血管生成抑制剂O-(氯乙酰-氨基甲酰)烟曲霉素(TNP-470,烟曲霉素的半合成类似物)对肿瘤生长和转移的影响。皮下注射TNP-470以剂量依赖性方式抑制肿瘤生长,B16BL6黑色素瘤、M5076网状细胞肉瘤、Lewis肺癌和Walker 256癌的肿瘤大小分别最大程度地减小至各自对照组的16%、10%、17%和4%。静脉注射时TNP-470的活性略弱于皮下注射。在所有测试的肿瘤中均观察到这种趋势。静脉注射(输注)TNP-470使荷Walker 256癌大鼠的寿命比对照组延长183%,而静脉推注仅使寿命延长47%。TNP-470以剂量依赖性方式减少静脉接种的B16BL6黑色素瘤的肺转移灶数量,以60 mg/kg、每周3次的剂量用TNP-470治疗后,转移灶数量减少至对照组的10%。采用该方案用TNP-470治疗的荷B16BL6肿瘤小鼠的平均存活时间比对照小鼠延长了5%。每天10 mg/kg的TNP-470也减少了从原发部位切除肿瘤后M5076肉瘤在肝脏中的转移灶数量。相同剂量的阿霉素仅略微减少了转移灶数量,尽管TNP-470和阿霉素对M5076肉瘤生长的抑制活性大致相当。每3天30 mg/kg的TNP-470使荷M5076肿瘤小鼠的平均存活时间比对照小鼠延长超过100%,而10 mg/kg的阿霉素最大程度地使平均存活时间延长20%。这些结果表明,血管生成抑制剂TNP-470对多种肿瘤的体内生长和转移具有强大的抑制活性。

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