首页> 外文OA文献 >Inhibition of breast cancer regrowth and pulmonary metastasis in nude mice by anti-gastric ulcer agent, irsogladine.
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Inhibition of breast cancer regrowth and pulmonary metastasis in nude mice by anti-gastric ulcer agent, irsogladine.

机译:抗胃溃疡药,伊索拉定抑制裸鼠乳腺癌再生和肺转移。

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摘要

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.
机译:伊索拉定在日本是一种常用的抗胃溃疡药,最近的体内研究表明它具有抗血管生成的特性。伊索拉定作为血管生成抑制剂的确切作用仍然不确定。在这项研究中,我们显示伊索拉定抑制乳腺癌的再生和肺转移,但对HUVEC细胞没有抗血管生成功能。 Irsogladine未能抑制HUVEC细胞的增殖,肾小管形成和uPA / MMP-1 mRNA表达。我们还检查了伊索拉定在无胸腺小鼠人乳腺癌转移的原位移植模型中的作用。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。口服伊索拉定或载剂。此后每天。在5周的时间内每天以120 mg / kg的剂量每天服用irsogladine对小鼠的体重没有影响。肿瘤的再生,肺转移的平均量和转移的数量分别被抑制了40%,48%和64%。这些结果表明,伊索拉定在乳腺癌佐剂治疗中可能有用。

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