Nozaki Shinichi, Maeda Mitsuaki, Tsuda Hiroyuki, Sledge George W
Division of Hematology/Oncology, Department of Medicine, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Breast Cancer Res Treat. 2004 Feb;83(3):195-9. doi: 10.1023/B:BREA.0000013996.49528.d8.
Irsogladine is a commonly used anti-gastric ulcer agent in Japan, and recent in vivo studies have shown it to have anti-angiogenic properties. The exact role of irsogladine as an inhibitor of angiogenesis remains uncertain. In this study, we show that irsogladine inhibited breast cancer regrowth and pulmonary metastasis but had no anti-angiogenic function against HUVEC cells. Irsogladine failed to inhibit proliferation, tubular formation, and the uPA/MMP-1 mRNA expression of HUVEC cells. We also examined the effect of irsogladine in an orthotopic transplant model of human breast cancer metastasis in athymic mice. Human MDA-MB-435 cells were injected into the mammary fat pads. After 9 weeks, the tumors were resected under general anesthesia. Irsogladine or vehicle was given p.o. daily thereafter. Daily administration of irsogladine at 120 mg/kg per day over a 5-week period had no effect on the body weight of the mice. Tumor regrowth, average volume of pulmonary metastases, and the number of metastases were inhibited by 40, 48 and 64%, respectively. These results suggest that irsogladine may be useful in the breast cancer adjuvant setting.
伊索格拉定是日本常用的抗胃溃疡药物,近期的体内研究表明它具有抗血管生成特性。伊索格拉定作为血管生成抑制剂的确切作用仍不确定。在本研究中,我们发现伊索格拉定可抑制乳腺癌的复发和肺转移,但对人脐静脉内皮细胞(HUVEC)没有抗血管生成功能。伊索格拉定未能抑制HUVEC细胞的增殖、管状形成以及尿激酶型纤溶酶原激活剂(uPA)/基质金属蛋白酶-1(MMP-1)mRNA表达。我们还在无胸腺小鼠的人乳腺癌转移原位移植模型中研究了伊索格拉定的作用。将人MDA-MB-435细胞注射到乳腺脂肪垫中。9周后,在全身麻醉下切除肿瘤。此后每天口服给予伊索格拉定或赋形剂。在5周的时间里,每天以120mg/kg的剂量给予伊索格拉定对小鼠体重没有影响。肿瘤复发、肺转移的平均体积和转移灶数量分别被抑制了40%、48%和64%。这些结果表明伊索格拉定在乳腺癌辅助治疗中可能有用。