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与顺二氯二氨铂(II)(顺铂)相比,评估3-氨基黄酮的顺铂(II)配合物对人淋巴细胞中P53和BAX基因表达的影响以及对细胞凋亡和坏死的诱导作用。

Evaluation of P53 and BAX gene expression and induction of apoptosis and necrosis by the cis-Pt(II) complex of 3-aminoflavone in comparison with cis-diamminedichloroplatinum(II) (cis-DDP) in human lymphocytes.

作者信息

Kosmider Beata, Zawlik Izabela, Liberski Pawel P, Osiecka Regina, Zyner Elzbieta, Ochocki Justyn, Bartkowiak Jacek

机构信息

Department of Cytogenetics and Plant Molecular Biology, University of Lodz, Banacha 12/16, 90-237 Lodz, Poland.

出版信息

Mutat Res. 2006 Apr 30;604(1-2):28-35. doi: 10.1016/j.mrgentox.2005.12.006. Epub 2006 Jan 27.

Abstract

Currently cis-diamminedichloroplatinum(II) (cis-DDP) is one of the most commonly applied compounds in chemotherapy of many types of cancer. However, a drawback is that its effectiveness presents with many side effects. Therefore, human normal lymphocytes were chosen as a model system to study cis-bis(3-aminoflavone)dichloroplatinum(II) (the cis-Pt(II) complex of 3-aminoflavone) in comparison with cis-DDP. We examined the effect of both tested compounds on cell viability and induction of apoptosis and necrosis. Trypan blue and acridine orange/ethidium bromide staining were carried out, as well as quantitative analysis of the apoptotic signal of P53 and BAX induction caused by the cis-Pt(II) complex of 3-aminoflavone in comparison with cis-DDP. cis-DDP induced a decrease of cell viability and led to a higher increase in necrosis and apoptosis than did the cis-Pt(II) complex of 3-aminoflavone. Moreover, at the molecular level cis-DDP increased P53 and BAX expression in comparison with the other tested compound. The cis-Pt(II) complex of 3-aminoflavone showed a weaker genotoxic effect in normal lymphocytes in comparison with cis-DDP, which was a stronger inducer of apoptosis and necrosis.

摘要

目前,顺二氯二氨铂(II)(顺铂)是多种癌症化疗中最常用的化合物之一。然而,一个缺点是其有效性伴随着许多副作用。因此,选择人类正常淋巴细胞作为模型系统,将顺二(3 - 氨基黄酮)二氯铂(II)(3 - 氨基黄酮的顺铂(II)配合物)与顺铂进行比较研究。我们检测了两种受试化合物对细胞活力以及凋亡和坏死诱导的影响。进行了台盼蓝和吖啶橙/溴化乙锭染色,以及与顺铂相比,对3 - 氨基黄酮的顺铂(II)配合物诱导的P53和BAX凋亡信号进行定量分析。与3 - 氨基黄酮的顺铂(II)配合物相比,顺铂导致细胞活力下降,坏死和凋亡增加得更多。此外,在分子水平上,与其他受试化合物相比,顺铂增加了P53和BAX的表达。与顺铂相比,3 - 氨基黄酮的顺铂(II)配合物在正常淋巴细胞中显示出较弱的遗传毒性作用,顺铂是更强的凋亡和坏死诱导剂。

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