首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >&ITIn vitro&IT studies on the tumorigenic potential of the halonitromethanes trichloronitromethane and bromonitromethane
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&ITIn vitro&IT studies on the tumorigenic potential of the halonitromethanes trichloronitromethane and bromonitromethane

机译:&Itin&IT研究卤代苯乙烷三氯硝基甲烷和溴代硝基甲烷的致摩洛胍潜力

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摘要

Epidemiological data indicate that chronic exposure to water disinfection by-products (DBPs) may result in increased risk of cancer. However, the real carcinogenic potential of individual DBPs is not well known. In this study, we assessed the in vitro carcinogenic potential of trichloronitromethane (TCNM) and bromonitromethane (BNM), two halonitromethanes (HNMs) commonly found in DBPs' mixtures at comparably high concentrations. Human lung BEAS-2B cells were exposed for 8 weeks to TCNM and BNM, and the acquisition of different in vitro cancer-like features was evaluated. The results indicate that long-term exposure to non-cytotoxic doses of TCNM and BNM did not cause carcinogenic transformation as indicated by the absence of morphological changes, no effects on cell growth, no changes in the level of matrix metalloproteinases (MMPs) secretion, and no increased anchorage-independent cell growth capacity. Furthermore, TCNM- and BNM-exposed BEAS-2B cells were unable to enhance tumour growth directly or by indirect influence of the surrounding stroma. Our results indicate that the carcinogenic effects of DBP mixtures cannot be attributed to the evaluated HNMs. This is the first study evaluating the cell transformation effects of TCNM and BNM under a long-term exposure scenario using suitable hallmarks of the cancer process.
机译:流行病学数据表明,慢性暴露于水消毒副产品(DBPS)可能导致癌症的风险增加。然而,单个Dbps的真实致癌潜力不是众所周知的。在本研究中,我们评估了三氯硝基甲烷(TCNM)和溴硝基甲烷(BNM)的体外致癌电位,在相当高浓度的Dbps混合物中常见的两种卤代噻吩(HNM)。将人肺BEA-2B细胞暴露于TCNM和BNM的8周,并评估了类似体外癌症样特征的采集。结果表明,长期暴露于非细胞毒剂量的TCNM和BNM并未引起致癌转化,如没有形态变化所表明的,对细胞生长没有影响,没有变化的基质金属蛋白酶(MMPS)分泌,并且没有增加锚定无关的细胞生长能力。此外,TCNM-和BNM暴露的BEA-2B细胞不能直接增强肿瘤生长或通过间接影响周围基质的间接影响。我们的结果表明,DBP混合物的致癌作用不能归因于评估的HNM。这是第一次研究使用合适的癌症过程的长期曝光场景评估TCNM和BNM的细胞转化效应。

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