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Mutagenic Tests Confirm That New Acetylacetonate Pt(II) Complexes Induce Apoptosis in Cancer Cells Interacting with Nongenomic Biological Targets

机译:诱变测试证实,新的乙酰丙酮酸Pt(II)复合物在与非基因组生物靶标相互作用的癌细胞中诱导凋亡。

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摘要

New platinum(II) complexes [PtCl(O,O′-acac)(L)] (1) and [Pt(O,O′-acac)(γ-acac)(L)] (2) (L = DMSO, a; DMS, b) containing a single chelated (O,O′-acac) (1), or one chelated and one σ-bonded (γ-acac) acetylacetonate (2) have been synthesized. The new Pt(II) complexes exhibited high in vitro cytotoxicity on cisplatin sensitive and resistant cell lines and showed negligible reactivity with nucleobases (Guo and 5′-GMP) but selective substitution of DMSO/DMS with soft biological nucleophiles, such as L-methionine. In order to assess the ability of the new complexes with respect to cisplatin to induce apoptosis by interaction with nongenomic targets, the Ames' test, a standard reverse mutation assay, was carried out on two Salmonella typhimurium strains (TA98 and TA100). Interestingly, the new complexes did not show the well-known mutagenic activity exhibited by cisplatin and are, therefore, able to activate apoptotic pathways without interacting with DNA.
机译:新的铂(II)配合物[PtCl(O,O'-acac)(L)](1)和[Pt(O,O'-acac)(γ-acac)(L)](2)(L = DMSO合成了一种包含单一螯合(O,O'-acac)(1)或一种螯合和一种σ键合(γ-acac)乙酰丙酮酸酯(2)的DMS,b)。新的Pt(II)配合物对顺铂敏感和耐药的细胞系表现出较高的体外细胞毒性,并且与核碱基(Guo和5'-GMP)的反应性微不足道,但可以用柔软的生物亲核试剂(如L-蛋氨酸)选择性取代DMSO / DMS。 。为了评估新复合物相对于顺铂通过与非基因组靶标相互作用诱导凋亡的能力,对两种鼠伤寒沙门氏菌菌株(TA98和TA100)进行了Ames试验(一种标准的反向突变试验)。有趣的是,新的复合物没有显示出顺铂所表现出的众所周知的诱变活性,因此能够激活凋亡途径而不与DNA相互作用。

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