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肿瘤启动子和血清对增殖蛋白mRNA诱导的联合作用:一种对糖精、2,3,7,8-四氯二苯并二恶英及其他在最低浓度下促进C3H/10T1/2细胞转化的化合物敏感的生物标志物。

Combined effects of tumor promoters and serum on proliferin mRNA induction: a biomarker sensitive to saccharin, 2,3,7,8-TCDD, and other compounds at minimal concentrations promoting C3H/10T1/2 cell transformation.

作者信息

Parfett Craig L

机构信息

Mutagenesis Section, Healthy Environments and Consumer Safety Branch, Health Canada, Environmental Health Centre, Ottawa, Ontario, Canada.

出版信息

J Toxicol Environ Health A. 2003 Oct 24;66(20):1943-66. doi: 10.1080/713853957.

Abstract

Increases in proliferin (PLF) gene family mRNA abundance and promotional effects in cell transformation assays are paired responses that follow exposures to diverse chemical and physical agents in the C3H/10T1/2 in vitro model of multi-stage carcinogenesis. This study measured PLF mRNA abundance changes over 1 to 3 d in response to several types of promoters that were previously unassessed for this effect. Saccharin is a known promoter of cell transformation in C3H/10T1/2 cell cultures, but unlike 12-O-tetradecanoylphorbol 13-acetate (TPA) or mezerein, PLF mRNA abundance increases were inconsistently detected following simple addition of saccharin to the culture medium. Consistent effects occurred when pretreatments with promoting concentrations of saccharin or sodium saccharin (1-13 mM) were combined with subsequent additions of serum or complete medium changes. When added at or near their lowest observed effect levels (LOELs) for transformation, other promoters of 10T1/2 cells such as formaldehyde (50-100 microM), diethylstilbesterol (DES) (0.5-30 microM), and 2,3,7,8-tetrachlorodibenzo-p-dioxin (2,3,7,8-TCDD) (4-40 pM) were shown to be inducers of both basal and serum-induced PLF mRNA levels. Acetaldehyde (300-900 microM) was comparable to formaldehyde as an inducer. In contrast to these various promoters, pretreatment with phenobarbital or methanol, both non-promoters in these cells, did not affect serum-induced PLF mRNA levels at concentrations up to 3 mM and 2 M, respectively. The published values for the LOELs of 17 promoters of cell transformation and the LOELs determined to date for PLF mRNA induction were highly correlated over a 1 billion - fold concentration range. The response of PLF mRNA is a short-term marker sensitive to the active concentration ranges of diverse chemical agents with promotional activity in C3H/10T1/2 cell transformation system.

摘要

在多阶段致癌作用的C3H/10T1/2体外模型中,增殖蛋白(PLF)基因家族mRNA丰度的增加以及在细胞转化试验中的促进作用是在暴露于多种化学和物理因子后出现的配对反应。本研究测定了在1至3天内,几种先前未评估过此效应的启动子作用下PLF mRNA丰度的变化。糖精是C3H/10T1/2细胞培养中已知的细胞转化启动子,但与12-O-十四酰佛波醇-13-乙酸酯(TPA)或大戟二萜醇不同,简单地向培养基中添加糖精后,PLF mRNA丰度的增加检测并不一致。当用促进浓度的糖精或糖精钠(1-13 mM)预处理,随后添加血清或更换完全培养基时,会出现一致的效应。当以或接近其在转化方面的最低观察效应水平(LOELs)添加时,10T1/2细胞的其他启动子,如甲醛(50-100 microM)、己烯雌酚(DES)(0.5-30 microM)和2,3,7,8-四氯二苯并对二恶英(2,3,7,8-TCDD)(4-40 pM),被证明是基础和血清诱导的PLF mRNA水平的诱导剂。乙醛(300-900 microM)作为诱导剂与甲醛相当。与这些不同的启动子相反,在这些细胞中均为非启动子的苯巴比妥或甲醇预处理,分别在高达3 mM和2 M的浓度下,不影响血清诱导的PLF mRNA水平。在10亿倍的浓度范围内,已发表的17种细胞转化启动子的LOEL值与迄今确定的PLF mRNA诱导的LOEL值高度相关。在C3H/10T1/2细胞转化系统中,PLF mRNA的反应是对具有促进活性的多种化学试剂的活性浓度范围敏感的短期标志物。

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