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Synthesis and characterization of platinum(II) oxadiazoline complexes and their in vitro antitumor activity in platinum-sensitive and -resistant cancer cell lines

机译:铂(II)恶二唑啉配合物的合成,表征及其在铂敏感性和耐药性癌细胞系中的体外抗肿瘤活性

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摘要

A series of platinum(II) complexes bearing Δ4-1,2,4-oxadiazoline ligands have been synthesized and characterized. Their in vitro antitumor activity has been assessed in platinum-sensitive and -resistant human ovarian cancer cell lines (PEO1, PEOCisR, PEOCarboR, and SK-OV3), as well as in colon cancer (SW948) and testicular cancer cell lines (N-TERA). All compounds tested showed potent cytotoxicity in the platinum-sensitive cell lines and retained activity in the cisplatin- and carboplatin-resistant lines, with IC50 values similar to the parental drug sensitive counterpart. We propose, therefore, that platinum(II) oxadiazoline complexes may possess a novel mechanism of action, which render them active in tumor cells, with resistance to currently used platinum anticancer agents.
机译:已经合成和表征了一系列带有Δ4-1,2,4-恶二唑啉配体的铂(II)配合物。已在对铂敏感和耐药的人卵巢癌细胞系(PEO1,PEOCisR,PEOCarboR和SK-OV3)以及结肠癌(SW948)和睾丸癌细胞系(N- TERA)。所有测试的化合物在铂敏感细胞系中均显示出强力的细胞毒性,在顺铂耐药和卡铂耐药系中具有保留的活性,IC50值与亲代药物敏感对应物相似。因此,我们建议,铂(II)恶二唑啉配合物可能具有新颖的作用机制,使其在肿瘤细胞中具有活性,并对目前使用的铂类抗癌药具有耐药性。

著录项

  • 作者

    Coley, HM; Sarju, J; Wagner, G;

  • 作者单位
  • 年度 2008
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  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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