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恢复卵巢早衰:基于网络药理学,槲皮素通过PI3K/AKT信号通路对抗伊马替尼诱导的细胞凋亡。

Revitalizing premature ovarian failure: quercetin counteracts imatinib-induced apoptosis via the PI3K/AKT signaling pathway based on network pharmacology.

作者信息

Ji Min, Weng Shiqi, Li Xia, Xiao Qin, Tong Yan, Zhou Yan, Luo Tao, Liu Zhaoxia

机构信息

Reproductive Medicine Center, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, 330006, China.

Department of Assisted Reproduction, Maternity and Child Health Hospital of Jiujiang, Jiujiang, Jiangxi, 332000, China.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2025 Jan;398(1):833-842. doi: 10.1007/s00210-024-03293-3. Epub 2024 Jul 29.

Abstract

As a commonly used first-line targeted drug, imatinib (Ima) is widely used first-line treatment for cancer patients. Patient survival is significantly prolonged, but Ima can cause premature ovarian failure (POF) and affect fertility. However, the underlying mechanism is unknown, and no effective method can be employed to improve this process. To investigate the effect of quercetin (Que) on Ima-induced POF and the underlying mechanism. The therapeutic impact of Que on Ima-induced POF in mice was clarified via molecular biology experiments and in vivo experiments in animals. To verify the underlying mechanism, network pharmacology was employed to construct a signaling network of Que-Ima-POF-related genes, followed by molecular biology and docking analysis. Network pharmacology analysis identified 38 therapeutic targets of Que in Ima-induced POF. The KEGG pathways of these genes were enriched for the phosphatidylinositol-3-kinase/protein kinase B (PI3K/Akt) signaling pathway. Molecular docking analysis revealed that the epidermal growth factor receptor (EGFR) is a shared target of Que, Ima, and POF and has strong binding affinity. Hematoxylin-eosin (HE) staining and ELISA confirmed that Que can partially restore the ovarian index and function of mice with Ima-induced POF. Western blot, TUNEL, and immunohistochemical staining confirmed that Que promoted the PI3K/Akt signaling pathway and reduced apoptosis in Ima-induced POF mice. Thus, Que could inhibit apoptosis in Ima-induced POF by activating the PI3K/Akt pathway.

摘要

作为一种常用的一线靶向药物,伊马替尼(Ima)被广泛用于癌症患者的一线治疗。患者生存期显著延长,但伊马替尼可导致卵巢早衰(POF)并影响生育能力。然而,其潜在机制尚不清楚,且尚无有效方法可改善这一过程。为研究槲皮素(Que)对伊马替尼诱导的POF的影响及其潜在机制。通过分子生物学实验和动物体内实验阐明了Que对伊马替尼诱导的小鼠POF的治疗作用。为验证潜在机制,采用网络药理学构建Que-Ima-POF相关基因的信号网络,随后进行分子生物学和对接分析。网络药理学分析确定了Que在伊马替尼诱导的POF中的38个治疗靶点。这些基因的KEGG通路在磷脂酰肌醇-3-激酶/蛋白激酶B(PI3K/Akt)信号通路中富集。分子对接分析表明,表皮生长因子受体(EGFR)是Que、伊马替尼和POF的共同靶点,且具有很强的结合亲和力。苏木精-伊红(HE)染色和ELISA证实,Que可部分恢复伊马替尼诱导的POF小鼠的卵巢指数和功能。蛋白质免疫印迹、TUNEL和免疫组织化学染色证实,Que促进了PI3K/Akt信号通路,并减少了伊马替尼诱导的POF小鼠的细胞凋亡。因此,Que可通过激活PI3K/Akt通路抑制伊马替尼诱导的POF中的细胞凋亡。

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