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Identification of hydrolyzable tannins (punicalagin, punicalin and geraniin) as novel inhibitors of hepatitis B virus covalently closed circular DNA

机译:鉴定可水解单宁(punicalagin,punicalin和geraniin)作为乙型肝炎病毒的新型抑制剂,共价闭合环状DNA

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The development of new agents to target HBV cccDNA is urgently needed because of the limitations of current available drugs for treatment of hepatitis B. By using a cell-based assay in which the production of HBeAg is in a cccDNA-dependent manner, we screened a compound library derived from Chinese herbal remedies for inhibitors against HBV cccDNA. Three hydrolyzable tannins, specifically punicalagin, punicalin and geraniin, emerged as novel anti-HBV agents. These compounds significantly reduced the production of secreted HBeAg and cccDNA in a dose-dependent manner in our assay, without dramatic alteration of viral DNA replication. Furthermore, punicalagin did not affect precore/core promoter activity, pgRNA transcription, core protein expression, or HBeAg secretion. By employing the cell-based cccDNA accumulation and stability assay, we found that these tannins significantly inhibited the establishment of cccDNA and modestly facilitated the degradation of preexisting cccDNA. Collectively, our results suggest that hydrolyzable tannins inhibit HBV cccDNA production via a dual mechanism through preventing the formation of cccDNA and promoting cccDNA decay, although the latter effect is rather minor. These hydrolyzable tannins may serve as lead compounds for the development of new agents to cure HBV infection. (C) 2016 Elsevier B.V. All rights reserved.
机译:由于当前可用于治疗乙型肝炎的药物的局限性,迫切需要开发靶向HBV cccDNA的新药物。通过使用基于细胞的测定方法,其中HBeAg的产生依赖于cccDNA的方式,我们筛选了一种源自中草药的HBV cccDNA抑制剂化合物库。出现了三种可水解的单宁,特别是punicalagin,punicalin和geraniin,作为新型抗HBV药物。在我们的测定中,这些化合物以剂量依赖的方式显着减少了分泌型HBeAg和cccDNA的产生,而没有病毒DNA复制的显着改变。此外,punicalagin不会影响前核心/核心启动子活性,pgRNA转录,核心蛋白表达或HBeAg分泌。通过使用基于细胞的cccDNA积累和稳定性测定,我们发现这些单宁酸显着抑制了cccDNA的建立,并适度促进了先前存在的cccDNA的降解。总的来说,我们的结果表明,可水解的丹宁酸通过阻止cccDNA的形成和促进cccDNA衰变的双重机制,通过双重机制抑制HBV cccDNA的产生,尽管后者的作用很小。这些可水解的单宁可以作为先导化合物,用于开发治疗HBV感染的新药物。 (C)2016 Elsevier B.V.保留所有权利。

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