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马兜铃酸形成的 DNA 加合物是暴露的独特生物标志物,并解释了上尿路上皮癌的起始阶段。

DNA Adducts Formed by Aristolochic Acid Are Unique Biomarkers of Exposure and Explain the Initiation Phase of Upper Urothelial Cancer.

机构信息

Department of Biochemistry, Faculty of Science, Charles University, Albertov 2030, CZ-12843 Prague 2, Czech Republic.

Analytical and Environmental Sciences Division, MRC-PHE Centre for Environment and Health, King's College London, London SE1 9NH, UK.

出版信息

Int J Mol Sci. 2017 Oct 14;18(10):2144. doi: 10.3390/ijms18102144.

Abstract

Aristolochic acid (AA) is a plant alkaloid that causes aristolochic acid nephropathy (AAN) and Balkan endemic nephropathy (BEN), unique renal diseases frequently associated with upper urothelial cancer (UUC). This review summarizes the significance of AA-derived DNA adducts in the aetiology of UUC leading to specific A:T to T:A transversion mutations (mutational signature) in AAN/BEN-associated tumours, which are otherwise rare in individuals with UCC not exposed to AA. Therefore, such DNA damage produced by AA-DNA adducts is one rare example of the direct association of exposure and cancer development (UUC) in humans, confirming that the covalent binding of carcinogens to DNA is causally related to tumourigenesis. Although aristolochic acid I (AAI), the major component of the natural plant extract AA, might directly cause interstitial nephropathy, enzymatic activation of AAI to reactive intermediates capable of binding to DNA is a necessary step leading to the formation of AA-DNA adducts and subsequently AA-induced malignant transformation. Therefore, AA-DNA adducts can not only be utilized as biomarkers for the assessment of AA exposure and markers of AA-induced UUC, but also be used for the mechanistic evaluation of its enzymatic activation and detoxification. Differences in AA metabolism might be one of the reasons for an individual's susceptibility in the multi-step process of AA carcinogenesis and studying associations between activities and/or polymorphisms of the enzymes metabolising AA is an important determinant to identify individuals having a high risk of developing AA-mediated UUC.

摘要

马兜铃酸(AA)是一种植物生物碱,可导致马兜铃酸肾病(AAN)和巴尔干地方性肾病(BEN),这两种独特的肾脏疾病常与上尿路上皮癌(UUC)相关。本文综述了 AA 衍生的 DNA 加合物在 UUC 发病机制中的意义,导致 AAN/BEN 相关肿瘤中特定的 A:T 到 T:A 颠换突变(突变特征),而在未接触 AA 的 UCC 个体中,这种突变特征很少见。因此,AA-DNA 加合物产生的这种 DNA 损伤是人类暴露和癌症发展(UUC)之间直接关联的一个罕见例子,证实了致癌物与 DNA 的共价结合与肿瘤发生有因果关系。虽然天然植物提取物 AA 的主要成分马兜铃酸 I(AAI)可能直接引起间质性肾炎,但 AAI 酶促激活为能够与 DNA 结合的反应性中间产物是导致 AA-DNA 加合物形成和随后 AA 诱导恶性转化的必要步骤。因此,AA-DNA 加合物不仅可作为评估 AA 暴露和 AA 诱导的 UUC 的标志物,还可用于其酶促激活和解毒的机制评估。AA 代谢的差异可能是个体在 AA 致癌多步骤过程中易感性的原因之一,研究代谢 AA 的酶的活性和/或多态性之间的关联是确定具有高风险发展 AA 介导的 UUC 的个体的重要决定因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24c9/5666826/d380c7d07544/ijms-18-02144-g001.jpg

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