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香烟烟雾会增加苯并(a)芘对人体细胞的DNA损伤,而含有迷迭香提取物的滤嘴则会降低自由基,从而减少这种损伤。

DNA damage by benzo(a)pyrene in human cells is increased by cigarette smoke and decreased by a filter containing rosemary extract, which lowers free radicals.

作者信息

Alexandrov Kroum, Rojas Margarita, Rolando Christian

机构信息

Université des Sciences et Technologies de Lille, Chimie Organique et Macromoléculaire and IFR 118, Protéomique, Modifications Post-trductionnelles et Glycobiologie, Villeneuve d'Ascq, France.

出版信息

Cancer Res. 2006 Dec 15;66(24):11938-45. doi: 10.1158/0008-5472.CAN-06-3277.

Abstract

We found previously that the human lung benzo(a)pyrene (BP)-7,8-diol-9,10-epoxide-N(2)-deoxyguanosine (BPDE-dG) adduct concentrate in the target bronchial cells. This adduct is now considered to be critical event in tumorigenesis by BP. In this study, we investigate the contribution of cigarette smoke on the BPDE-dG formation. In a cell-free system, the amount of (-)-anti-BPDE-dG adduct increased linearly with concentration of cigarette smoke in the presence of (+)-BP-7,8-diol. Catalase and superoxide dismutase inhibited its formation by >80%. When MCF-7 cells were treated for 2 hours with the (+)-BP-7,8-diol, cigarette smoke increased dose dependently the formation of (-)-anti-BPDE-dG and decreased the cytochrome P450 (CYP)-dependent formation of (+)-r-7,t-8-dihydroxy-c-9,10-oxy-7,8,9,10-tetrahydro-BP the adduct. Then, cells were treated for up to 1 day with BP and then exposed for 2 hours with cigarette smoke. During these 2 hours, there are twice the increase in the adduct formation in cells treated with cigarette smoke compared with levels in nontreated cells due to CYP activity. Thus, cigarette smoke containing reactive oxygen species may activate the second step of BP metabolic way, leading to the formation of BPDE-dG adduct. Cigarette smoke thus seems may be in part responsible for the formation of the critical lung tumorigenic adduct. Finally, modified cigarette filter containing rosemary extract decreases by >70% of the BPDE-dG adducts level due to the cigarette smoke in MCF-7 cells. This approach may lead to decreasing lung cancer risk in addicted smokers.

摘要

我们之前发现,人肺中的苯并(a)芘(BP)-7,8-二醇-9,10-环氧化物-N(2)-脱氧鸟苷(BPDE-dG)加合物集中在目标支气管细胞中。现在认为这种加合物是BP致癌过程中的关键事件。在本研究中,我们调查了香烟烟雾对BPDE-dG形成的影响。在无细胞体系中,在存在(+)-BP-7,8-二醇的情况下,(-)-反式-BPDE-dG加合物的量随香烟烟雾浓度呈线性增加。过氧化氢酶和超氧化物歧化酶对其形成的抑制率>80%。当MCF-7细胞用(+)-BP-7,8-二醇处理2小时时,香烟烟雾剂量依赖性地增加了(-)-反式-BPDE-dG的形成,并降低了细胞色素P450(CYP)依赖性的(+)-r-7,t-8-二羟基-c-9,10-氧代-7,8,9,10-四氢-BP加合物的形成。然后,细胞先用BP处理长达1天,再用香烟烟雾暴露2小时。在这2小时内,由于CYP活性,与未处理细胞相比,用香烟烟雾处理的细胞中加合物形成增加了两倍。因此,含有活性氧的香烟烟雾可能激活BP代谢途径的第二步,导致BPDE-dG加合物的形成。因此,香烟烟雾似乎可能部分导致关键的肺致癌加合物的形成。最后,含有迷迭香提取物的改良香烟滤嘴使MCF-7细胞中由于香烟烟雾产生的BPDE-dG加合物水平降低了>70%。这种方法可能会降低成瘾吸烟者患肺癌的风险。

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