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首页> 外文期刊>International Journal of Molecular Sciences >Pharmacological Applications of Nrf2 Inhibitors as Potential Antineoplastic Drugs
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Pharmacological Applications of Nrf2 Inhibitors as Potential Antineoplastic Drugs

机译:Nrf2抑制剂作为潜在抗肿瘤药物的药理应用

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摘要

Oxidative stress (OS) is associated with many diseases ranging from cancer to neurodegenerative disorders. Nuclear factor-erythroid 2 p45-related factor 2 (Nrf2) is one of the most effective cytoprotective controller against OS. Modulation of Nrf2 pathway constitutes a remarkable strategy in the antineoplastic treatments. A big number of Nrf2-antioxidant response element activators have been screened for use as chemo-preventive drugs in OS associated diseases like cancer even though activation of Nrf2 happens in a variety of cancers. Research proved that hyperactivation of the Nrf2 pathway produces a situation that helps the survival of normal as well as malignant cells, protecting them against OS, anticancer drugs, and radiotherapy. In this review, the modulation of the Nrf2 pathway, anticancer activity and challenges associated with the development of an Nrf2-based anti-cancer treatment approaches are discussed.
机译:氧化应激(OS)与许多疾病相关,从癌症到神经退行性疾病。核因子-类胡萝卜素2 p45相关因子2(Nrf2)是针对OS的最有效的细胞保护控制器之一。 Nrf2途径的调制构成了抗肿瘤治疗中的一项重要策略。尽管Nrf2的激活发生在多种癌症中,但已筛选出大量Nrf2抗氧化剂反应因子激活剂用作与OS相关的疾病(如癌症)的化学预防药物。研究证明,Nrf2途径的过度激活会产生一种状况,有助于正常细胞和恶性细胞的存活,保护它们免受OS,抗癌药物和放射疗法的侵害。在这篇综述中,讨论了Nrf2途径的调节,抗癌活性以及与基于Nrf2的抗癌治疗方法的发展相关的挑战。

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