首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Evaluation of cisplatin + 5-FU, carboplatin + 5-FU, and ifosfamide + epirubicine regimens using the micronuclei test and nuclear abnormalities in the buccal mucosa.
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Evaluation of cisplatin + 5-FU, carboplatin + 5-FU, and ifosfamide + epirubicine regimens using the micronuclei test and nuclear abnormalities in the buccal mucosa.

机译:使用微核试验和颊黏膜核异常评估顺铂+ 5-FU,卡铂+ 5-FU和异环磷酰胺+表柔比星疗法。

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摘要

In the present work, the micronuclei (MN) test was performed in buccal mucosal samples from patients with cancer, with (pre- and post-treatment) and without genotoxic chemotherapy (GC), identified micronucleated cells (MNC) and nuclear abnormalities (binucleated cells (BN), pycnosis (PN), broken-egg karyolysis (KL)).The objective was to evaluate the genotoxicity of cisplatin+5-Fluorouracil (5-FU), carboplatin (CBP)+5-Fluorouracil, and ifosfamide (IFO)+epirubicine (EPI) regimens.The ifosfamide+epirubicine regimen described here produced a micronucleogenic effect, whereas the regimens using platinum compounds were cytotoxic for buccal mucosal cells, which probably explains the absence of increase of micronucleated cells in these samples compared with basal levels.In patients with cancer (with and without genotoxic chemotherapy), the numbers of micronucleated cells, pycnosis and karyolysis increased, together with a decrease in binucleated cells and chromatin-condensed. On the other hand, as consequence of the cytotoxicity of the drugs, the number of binucleated cells decreased and the number of karyolytic cells increased. These results could be used as a cytotoxicity marker in future studies for different drugs.
机译:在目前的工作中,微核(MN)测试是在癌症患者的颊粘膜样本中进行的,治疗前(治疗后)和未进行遗传毒性化学疗法(GC),鉴定出微核细胞(MNC)和核异常(双核细胞(BN),脓疱病(PN),卵裂核解(KL))。目的是评估顺铂+ 5-氟尿嘧啶(5-FU),卡铂(CBP)+ 5-氟尿嘧啶和异环磷酰胺( IFO)+厄比斯比星(EPI)方案。此处描述的异环磷酰胺+厄比斯比星方案产生了微核基因作用,而使用铂化合物的方案对颊粘膜细胞具有细胞毒性,这可能解释了这些样品与基底膜相比没有微核细胞增加在患有癌症的患者中(接受或不接受基因毒性化疗),微核细胞,脓疱病和核溶解的数量增加,双核细胞减少和染色质浓缩。另一方面,由于药物的细胞毒性,双核细胞的数量减少,溶核细胞的数量增加。这些结果可用作将来对不同药物的研究的细胞毒性标记。

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