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使用体外Bhas 42细胞转化试验对电子烟和香烟进行比较性肿瘤促进评估。

Comparative tumor promotion assessment of e-cigarette and cigarettes using the in vitro Bhas 42 cell transformation assay.

作者信息

Breheny Damien, Oke Oluwatobiloba, Pant Kamala, Gaça Marianna

机构信息

British American Tobacco, Research and Development, Southampton, UK.

Department of Genetic Toxicology, Bioreliance Corporation, Rockville, Maryland.

出版信息

Environ Mol Mutagen. 2017 May;58(4):190-198. doi: 10.1002/em.22091.

Abstract

In vitro cell transformation assays (CTA) are used to assess the carcinogenic potential of chemicals and complex mixtures and can detect nongenotoxic as well as genotoxic carcinogens. The Bhas 42 CTA has been developed with both initiation and promotion protocols to distinguish between these two carcinogen classes. Cigarette smoke is known to be carcinogenic and is positive in in vitro genotoxicity assays. Cigarette smoke also contains nongenotoxic carcinogens and is a tumour promoter and cocarcinogen in vivo. We have combined a suite of in vitro assays to compare the relative biological effects of new categories of tobacco and nicotine products with traditional cigarettes. The Bhas promotion assay has been included in this test battery to provide an in vitro surrogate for detecting tumor promoters. The activity of an electronic cigarette (e-cigarette; Vype ePen) was compared to that of a reference cigarette (3R4F) in the promotion assay, using total particulate matter (TPM)/aerosol collected matter (ACM) and aqueous extracts (AqE) of product aerosol emissions. 3R4F TPM was positive in this assay at concentrations ≥6 µg/mL, while e-cigarette ACM did not have any promoter activity. AqE was found to be a lesssuitable test matrix in this assay due to high cytotoxicity. This is the first study to use the Bhas assay to compare tobacco and nicotine products and demonstrates the potential for its future application as part of a product assessment framework. These data add to growing evidence suggesting that e-cigarettes may provide a safer alternative to traditional cigarettes. Environ. Mol. Mutagen. 58:190-198, 2017. © 2017 Wiley Periodicals, Inc.

摘要

体外细胞转化试验(CTA)用于评估化学物质和复杂混合物的致癌潜力,能够检测非遗传毒性致癌物以及遗传毒性致癌物。Bhas 42 CTA已通过启动和促进方案开发出来,以区分这两类致癌物。已知香烟烟雾具有致癌性,并且在体外遗传毒性试验中呈阳性。香烟烟雾还含有非遗传毒性致癌物,并且在体内是肿瘤促进剂和辅助致癌物。我们结合了一系列体外试验,以比较新型烟草和尼古丁产品与传统香烟的相对生物学效应。该测试组合中包含Bhas促进试验,以提供一种检测肿瘤促进剂的体外替代方法。在促进试验中,使用产品气溶胶排放的总颗粒物(TPM)/气溶胶收集物(ACM)和水提取物(AqE),将电子烟(Vype ePen)的活性与参比香烟(3R4F)进行比较。在该试验中,3R4F TPM在浓度≥6μg/mL时呈阳性,而电子烟ACM没有任何促进活性。由于高细胞毒性,发现AqE在此试验中是不太合适的测试基质。这是第一项使用Bhas试验比较烟草和尼古丁产品的研究,并证明了其作为产品评估框架一部分的未来应用潜力。这些数据进一步证明电子烟可能是传统香烟的一种更安全的替代品。《环境与分子突变》58:190 - 198,2017年。©2017威利期刊公司

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f7/5435921/33da7030d2af/EM-58-190-g001.jpg

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