钌复合物 KP1019 在乳腺癌细胞迁移和侵袭模型中的抑制作用

Metal-Based Drugs Pub Date : 2009-01-01 Epub Date: 2009-09-17 DOI:10.1155/2009/681270
A Bergamo, A Masi, M A Jakupec, B K Keppler, G Sava
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引用次数: 0

摘要

反式吲唑-[四氯双(1H-吲唑)钌酸盐(III)](KP1019 或 FFC14A)是第二种进入临床试验阶段的钌化合物,它在体外肿瘤侵袭和转移模型中的作用表明,这种化合物的抗肿瘤作用可能还包括调节细胞行为,尽管其细胞毒性似乎比这些作用更主要。不过,与咪唑类似物 KP418 相比,KP418 更具优势,能够控制体外细胞生长,在某些情况下还能控制体内肿瘤的发展。这些结果表明,KP1019 的活性主要是由于对肿瘤细胞的直接细胞毒性作用,这在体内原发性肿瘤生长中也很明显,而对癌细胞生物学行为的调节作用可能存在,但可能只起部分作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Inhibitory Effects of the Ruthenium Complex KP1019 in Models of Mammary Cancer Cell Migration and Invasion.

Inhibitory Effects of the Ruthenium Complex KP1019 in Models of Mammary Cancer Cell Migration and Invasion.

Inhibitory Effects of the Ruthenium Complex KP1019 in Models of Mammary Cancer Cell Migration and Invasion.

Inhibitory Effects of the Ruthenium Complex KP1019 in Models of Mammary Cancer Cell Migration and Invasion.

The effects of indazolium trans-[tetrachlorobis(1H-indazole)ruthenate(III)] (KP1019, or FFC14A), the second ruthenium compound that entered clinical trials, in an in vitro model of tumour invasion and metastasis show that the antitumour effects of this compound might include also the modulation of cell behaviour although its cytotoxicity appears to be predominant over these effects. The comparison with its imidazole analogue KP418 shows however its superiority, being able to control in vitro cell growth and in some instances also in vivo tumour development. These results suggest that the activity of KP1019 is predominantly due to direct cytotoxic effects for tumour cells, evident also in vivo on primary tumour growth and that the effects on modulation of the biological behaviour of the cancer cell can be present but might have only a partial role.

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