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Importance of phase 2 gene regulation in protection against electrophile and reactive oxygen toxicity and carcinogenesis

机译:相2基因调控对电泳和反应性氧毒性和致癌作用保护的重要性

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A growing body of evidence supports the view that induction of phase 2 enzymes is an effective strategy for lowering the susceptibility of animals and their cells to the carcinogenic effects of electrophiles and reactive oxygen intermediates, and thereby decreasing the risk of developing cancer. Many inducers of phase 2 genes are present in edible plants. They belong to a variety of chemical classes that have few apparent chemical similarities, and are therefore unlikely to react with a structurallycomplementary cellular receptor. However, all inducers are chemically reactive and can react with thiol groups by alkylation or by oxidoreduction. Measurement of potency of induction of NAD(P)H: quinone reductase in marine hepatoma cells provides a simple and reliable bioassay for isolating inducers from plant extracts and for directing a synthetic program seeking to develop more effective analogues of known inducers. The mechanism of induction involves the ability of inducers to enter the cytoplasm anddisrupt the complex between the transcription factor Nrf2 and Keapl, a cysteine-rich protein that is anchored to the actin cytoskeleton. Upon disruption of the complex. Nrf2 migrates to the nucleus where it binds to the ARE (Antioxidant Response Element) present in the upstream regions of many phase 2 genes and activates transcription of these genes. With the use of overexpresssed and purified Keapl, we have established that this cysteine-rich protein contains a small number of highly reactive cysteine residues that appear to be the sensors for inducers. Reaction of these thiol groups with inducers could cause a conformational change leading to dissociation of the Nrf2-Keapl complex.
机译:越来越多的证据支持认为,相2酶的诱导是一种有效的策略,用于降低动物及其细胞对电子手机和反应性氧中间体的致癌作用的有效策略,从而降低发展癌症的风险。在食用植物中存在许多相2基因的诱导剂。它们属于具有很少表观化学相似性的各种化学类,因此不太可能与结构互动的细胞受体反应。然而,所有诱导剂都是化学反应性的,并且可以通过烷基化或通过氧化反应与硫醇基团反应。测量NAD诱导效力(P)H:海洋肝癌细胞中的醌还原酶提供了一种简单可靠的生物测定,用于分离植物提取物的诱导剂,并指导寻求开发更有效的已知诱导剂的类似物。诱导机制涉及诱导者进入细胞质的能力,并抑制转录因子NRF2和Keapl之间的复合物,富含半胱氨酸的蛋白质,其锚定在肌动蛋白细胞骨架上。破坏复杂。 NRF2迁移到核,其中其与存在于许多相2基因的上游区域中的(抗氧化剂响应元件)并激活这些基因的转录。通过使用过表达和纯化的Keapl,我们已经确定这种富含半胱氨酸的蛋白质含有少量高度反应性的半胱氨酸残基,似乎是诱导剂的传感器。这些硫醇基团与诱导剂的反应可能导致构象变化导致NRF2-KEAPL复合物的解离。

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