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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Genotoxicity testing of combined treatment with cisplatin, bleomycin, and 5-fluorouracil in somatic cells of Drosophila melanogaster.
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Genotoxicity testing of combined treatment with cisplatin, bleomycin, and 5-fluorouracil in somatic cells of Drosophila melanogaster.

机译:果蝇马六甲酸细胞体细胞组合治疗的基因毒性试验。

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The simultaneous treatment with the cross-linking agent cisplatin, the radiomimetic antitumoral drug bleomycin, and the anti-metabolite drug 5-fluorouracil has been used as a regimen to treat patients with squamous cell carcinoma of the head and neck. Considering that these drugs interact directly with DNA, one of the important late-occurring complications from treatment of primary malignancies is the therapy-related secondary cancers as a result of the genotoxic activity of the drugs on normal cells. In this sense, the genotoxicity of this combination was evaluated using the wing somatic mutation and recombination test in Drosophila melanogaster. The mutant spots observed in marker-heterozygous and balancer-heterozygous flies were compared in order to quantitatively and qualitatively estimate the genotoxic effect of these drugs. Cisplatin (0.003 and 0.006mM), bleomycin (0.005 and 0.01mM), and both combinations preferentially induced recombinational events, while mutation is the major event regarding the genetic toxicity of 5-fluorouracil (0.025 and 0.05mM). The combination of these drugs produced synergistic and antagonistic genotoxic effects, depending on the concentrations used, which could impose a higher risk of secondary effects associated with their genotoxic effects, emphasizing the importance of long-term monitoring in patients being treated with these drugs.
机译:用交联剂顺铂同时治疗,辐射染色抗肿瘤药物筛选和抗代谢物药物5-氟尿嘧啶已被用作治疗头部和颈部鳞状细胞癌患者的方案。考虑到这些药物直接与DNA相互作用,主要恶性肿瘤治疗的重要迟到的并发症之一是治疗相关的二次癌症,因为药物对正常细胞的遗传毒性活性。从这个意义上讲,使用翅膀躯体突变和在果蝇黑素转酯中的重组试验评估这种组合的遗传毒性。比较在标志物 - 杂合和平衡杂合苍蝇中观察到的突变斑,以定量和定性估计这些药物的遗传毒性作用。顺铂(0.003和0.006mm),Bleomycin(0.005和0.01mm),并且两种组合优先诱导重组事件,而突变是关于5-氟尿嘧啶的遗传毒性(0.025和0.05mm)的主要事件。这些药物的组合产生了协同和拮抗遗传毒性作用,这取决于所用的浓度,这可能征收与遗传毒性效应相关的次要影响的风险,强调在用这些药物治疗的患者中长期监测的重要性。

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