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Dithiolethiones for cancer chemoprevention: where do we stand?

机译:用于癌症化学预防的二硫代硫酮:我们站在哪里?

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Dithiolethiones are a well-known class of cancer chemopreventive agents; the key mechanism of action of dithiolethiones involves activation of Nrf2 signaling and induction of phase II enzymes. In the past, attention has been focused mainly on 4-methyl-5-pyrazinyl-3H-1,2-dithiole-3-thione (oltipraz), which showed ability as a wide-spectrum inhibitor of chemical carcinogenesis in preclinical models. However, clinical trials of oltipraz have shown questionable efficacy, and at the high doses employed in such studies, significant side effects were observed. Dithiolethiones that are markedly more effective and potent than oltipraz in both induction of phase II enzymes and inhibition of chemical carcinogenesis in preclinical studies have been identified, and these compounds have shown pronounced organ specificity in vivo. Further investigation of these compounds may lead to development of effective and safe agents for cancer prevention in humans.
机译:二硫代硫酮是一类众所周知的癌症化学预防剂。二硫代乙硫酮作用的关键机制涉及Nrf2信号的激活和II期酶的诱导。过去,注意力主要集中在4-甲基-5-吡嗪基-3H-1,2-二硫代-3-硫酮(oltipraz),在临床前模型中显示出作为化学致癌作用的广谱抑制剂的能力。然而,oltipraz的临床试验显示出可疑的疗效,并且在此类研究中使用高剂量时,观察到了明显的副作用。在临床前研究中,已发现在II期酶的诱导和化学致癌作用的抑制方面,二硫代硫酮比oltipraz更为有效和有效,并且这些化合物在体内显示出明显的器官特异性。对这些化合物的进一步研究可能会导致开发出有效且安全的人类癌症预防剂。

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