雷公藤甲素对卵巢靶向CASP3、TP53和MYC诱导女性生殖毒性

Guang Zheng, Xue Yan, Yun Yang, He Zhang, Hongtao Guo, Junping Zhan, Xiaojuan He
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引用次数: 0

摘要

雷公藤甲素是从中草药雷公藤中提取的一种重要活性化合物,尽管具有积极的治疗作用,但其雌性生殖毒性仍阻碍了其临床应用,其毒性机制尚不清楚。为了解决雌性生殖毒性的机制,一种直观的方法是探索涉及靶向蛋白和相关卵巢表达蛋白的生物分子网络。本研究首先分析雷公藤甲素的靶蛋白及其生物学功能。然后,重点研究细胞周期负调控的富集过程,提取靶蛋白与卵巢中表达的参与细胞周期负调控的蛋白,形成雌性生殖毒性分子网络。最后,CASP3、TP53和MYC的三个靶向蛋白被强调为女性生殖毒性的主要原因。进一步分析表明,这3种靶蛋白可进一步调控21种卵巢表达蛋白,并参与相关过程。本研究为雷公藤甲素的雌性生殖毒性提供了明确的分子水平机制,可用于预防毒性的同时保持其治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CASP3, TP53, and MYC Targeted by Triptolide towards Ovary Induce Female Reproductive Toxicity
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.
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