首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >Cadmium affects genes involved in growth regulation during two-stage transformation of Balb/3T3 cells.
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Cadmium affects genes involved in growth regulation during two-stage transformation of Balb/3T3 cells.

机译:镉影响Balb / 3T3细胞两阶段转化过程中涉及生长调节的基因。

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Cadmium (Cd), a carcinogenic metal in human and rodents, has been shown to transform cells in vitro. However, the carcinogenic mechanisms of Cd as a mutagen and/or promoter are not well clarified. We already reported that CdCl2 in a range of 1.5 approximately 360 ng/ml enhanced transformation of Balb/3T3 A31 cells induced by N-methyl-N'-nitro-N-nitrosoguanidine (MNNG, 0.1 microg/ml) in a dose-dependent manner (Fang et al., Toxicol. In Vitro 15(3) (2001a) 51-7). In previous study, we observed that Cd stimulated cell proliferation on MNNG-initiated cells through inactivation of p53 and p27 and increase of proliferating cell nuclear antigen (PCNA) expression after 24 h treatment (Fang et al., Toxicology 163 (2001b) 175-84). The aim of this study is to further elucidate the long-term effect of Cd in terms of cell cycle control gene expressions during the promotion stage of in vitro two-stage transformation. For the purpose, we determined the expression levels of the genes involved in growth regulation, such as p53, p27, c-myc, mdm2, cyclins D1 and B1, CDK4, and PCNA in the cells treated with Cd for 14 days after MNNG-initiation. In MNNG+CdCl2 group, cells apparently expressed cellular tumor antigen p53 mRNA, but did not express the wild-type p53 protein; the protein and mRNA levels of p27 were reduced apparently in the cells of MNNG+CdCl2 group compared to the cells of control and MNNG group. In addition, the protein levels of cyclin D1, CDK4, PCNA, c-myc, and mdm2, and cyclin B1 mRNA level were higher in MNNG+CdCl2 group than control and MNNG group. Together with previous data (Fang et al., Toxicology 163 (2001b) 175-84), our results indicated that during the transformation process of MNNG-treated cells, Cd may activate oncogenes such as c-myc, mdm2, and cellular tumor antigen p53, inhibit the tumor suppressor genes such as wild-type p53 and p27, and consequently accelerate the proliferation of initiated cells. This work firstly demonstrates that Cd affects the genes involved in growth regulation on initiated cells during the promotion stage of in vitro cell transformation.
机译:镉(Cd)是人和啮齿动物中的致癌金属,已显示出可以在体外转化细胞。但是,尚不清楚Cd作为诱变剂和/或启动子的致癌机理。我们已经报道了CdCl2在1.5约360 ng / ml的范围内增强了剂量依赖性的N-甲基-N'-硝基-N-亚硝基胍(MNNG,0.1 microg / ml)诱导的Balb / 3T3 A31细胞转化(Fang等,Toxicol.In Vitro 15(3)(2001a)51-7)。在先前的研究中,我们观察到Cd通过在处理24小时后灭活p53和p27并增加增殖细胞核抗原(PCNA)的表达来刺激MNNG诱导的细胞增殖(Fang等人,Toxicology 163(2001b)175- 84)。这项研究的目的是进一步阐明Cd在体外两阶段转化促进阶段的细胞周期控制基因表达方面的长期作用。为此,我们确定了在MNNG-处理14天后用Cd处理的细胞中涉及生长调节的基因(例如p53,p27,c-myc,mdm2,cyclins D1和B1,CDK4和PCNA)的表达水平。引发。 MNNG + CdCl2组细胞明显表达细胞肿瘤抗原p53 mRNA,但不表达野生型p53蛋白。与对照组和MNNG组相比,MNNG + CdCl2组细胞p27蛋白和mRNA水平明显降低。另外,MNNG + CdCl2组细胞周期蛋白D1,CDK4,PCNA,c-myc和mdm2的蛋白水平以及细胞周期蛋白B1mRNA水平高于对照组和MNNG组。连同先前的数据(Fang等人,Toxicology 163(2001b)175-84),我们的结果表明,在MNNG处理的细胞转化过程中,Cd可能激活癌基因,例如c-myc,mdm2和细胞肿瘤抗原p53抑制野生型p53和p27等肿瘤抑制基因,从而加速起始细胞的增殖。这项工作首先证明了Cd在体外细胞转化的促进阶段会影响参与启动细胞生长调节的基因。

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