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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Anti-cancer activity of a novel palladium(II) complex on human breast cancer cells in vitro and in vivo.
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Anti-cancer activity of a novel palladium(II) complex on human breast cancer cells in vitro and in vivo.

机译:新型钯(II)配合物在体外和体内对人乳腺癌细胞的抗癌活性。

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摘要

Anti-cancer effects of a newly-synthesized palladium(II) complex, [Pd(sac)(terpy)](sac).4H(2)O (sac = saccharinate, and terpy = 2,2':6',2''-terpyridine), were tested against human breast cancer cell lines, MCF-7 and MDA-MB-231. The Pd complex had a strong anti-growth effect in a dose- and time-dependent manner in vitro. This effect was also confirmed by the experiment performed on Balb/c mice in vivo. The IC(50) values were 0.09 muM for MDA-MB-231 and 3.05 muM for MCF-7. It was also very effective in disrupting the formation of MDA-MB-231 tubules on matrigel, indicative of a putative anti-invasive activity. It induced apoptosis via the cell death genes of DR4 and DR5. In conclusion, this newly-synthesized Pd (II) complex represents a potentially active novel drug for the breast cancer treatment.
机译:新合成的钯(II)复合物[Pd(sac)(terpy)](sac).4H(2)O(sac =糖精,terpy = 2,2':6',2)的抗癌作用对人乳腺癌细胞系MCF-7和MDA-MB-231进行了测试。 Pd复合物在体外具有剂量和时间依赖性的强抗生长作用。通过在体内对Balb / c小鼠进行的实验也证实了这种效果。对于MDA-MB-231,IC(50)值为0.09μM,对于MCF-7,IC(50)值为3.05μM。它在破坏基质胶上的MDA-MB-231小管形成方面也非常有效,表明推定的抗侵袭活性。它通过DR4和DR5的细胞死亡基因诱导凋亡。总之,这种新合成的Pd(II)配合物代表了一种用于乳腺癌治疗的潜在活性新药。

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