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CASP3, TP53, and MYC Targeted by Triptolide towards Ovary Induce Female Reproductive Toxicity

机译:Casp3,TP53和Myc由雷公藤内酯瞄准卵巢诱导女性生殖毒性

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Triptolide is an important active compound derived from Chinese herbal medicine Tripterygium wilfordii Hook f. Despite its positive therapeutic effects, the female reproductive toxicity is still blocking its clinical application with its toxicity mechanism is still obscure. In order to tackle the mechanism of female reproductive toxicity, one intuitive approach is to explore the biological molecule network involving targeted proteins and associated ovary expressed proteins. In this study, triptolide's target proteins and their biological functions were analyzed first. Then, focused on the enriched process of negative regulation of cell cycle, targeted proteins, together with proteins expressed in ovary which are contributed in negative regulation of cell cycle were extracted so as to form the female reproductive toxicity molecule network. Finally, three targeted proteins of CASP3, TP53, and MYC were highlighted as the leading causation of female reproductive toxicity. Further analysis indicated that these 3 target proteins can further regulate 21 ovary expressed proteins which also participate in associated processes. This study provides specified molecule level mechanism the female reproductive toxicity of triptolide which can be used to prevent toxicity while keeping its therapeutic effects.
机译:雷丝酮是衍生自中草药泰格尼亚威尔福德钩F的重要活性化合物。尽管其阳性治疗效果,但雌性生殖毒性仍在阻塞其临床应用,其毒性机制仍然模糊不清。为了解决女性生殖毒性的机制,一种直观的方法是探讨涉及靶向蛋白质和相关卵巢表达蛋白的生物分子网络。在本研究中,首先分析了雷公藤苷的靶蛋白及其生物学功能。然后,对细胞周期的富集过程的浓缩过程,靶向蛋白质与卵巢表达的蛋白质一起提取,这些蛋白质在细胞周期的阴性调节中有助于形成雌性生殖毒性分子网络。最后,突出了三种靶向蛋白质的Casp3,TP53和Myc作为女性生殖毒性的主要原因。进一步的分析表明,这些3个靶蛋白可以进一步调节21种卵巢表达的蛋白,该蛋白也参与相关方法。该研究提供了指定的分子水平机制,其胎旋翼的女性生殖毒性,可用于预防毒性,同时保持其治疗效果。

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