Xiaozheng pill exerts an anti-mammary hyperplasia effect through Raf/ERK/ELK and HIF-1α/bFGF pathways

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2023-11-01 DOI:10.1016/j.jtcme.2023.05.002
Yu-fei Liu , Tian An , Hong Yu , Ying-yi Fan , Xiao-hua Pei
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Abstract

Background and aim

The purpose of this study is to explore whether the Xiaozheng pill (XZP) has the effect of anti-hyperplasia of mammary glands (HMG) and to identify the related signaling pathways.

Experimental procedure

We analyzed the effective chemical components of the XZP, as well as the key chemical components, key proteins, main biological processes, and pathways in the treatment of HMG; Secondly, the levels of Estradiol (E2), Follicle-stimulating hormone (FSH), Luteinizing hormone (LH), Progesterone (P), Raf/ERK/ELK and HIF-1α/bFGF pathways related proteins were detected; Finally, the effect of XZP on metabolites was analyzed by metabolomics.

Results and conclusion

In this study, we identified key targets and pathways for XZP therapy of HMG, including EGFR, VEGFA, ER, and Ras signaling pathways. Animal experiments show that XZP can reduce the levels of E2, LH, and FSH and increase the expression of P in HMG mice. XZP can restore the normal structure of breast tissue and reduce ERα, ERβ, and PR expression in breast tissue. In addition, metabolomics results show that XZP also regulates HMG metabolites, including HIF-1α and metabolic pathways. The Western blot results showed that XZP intervention can reduce the protein expression of p-Raf1, Raf1, p-ERK1/2, ERK1/2, ELK, HIF-1α, and bFGF in the breast tissue of HMG mice. XZP may eliminate abnormal breast hyperplasia through inhibition of apoptosis and angiogenesis, which may be linked with the regulation of the Raf/ERK/ELK and HIF-1α/bFGF signaling pathways in HMG mice. These results suggest that XZP treatment may be beneficial for the management of HMG.

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消正丸通过Raf/ERK/ELK和HIF-1α/bFGF通路发挥抗乳腺增生作用
背景与目的探讨消正丸(XZP)是否具有抗乳腺增生(HMG)的作用,并确定相关信号通路。实验程序分析了XZP的有效化学成分,以及治疗HMG的关键化学成分、关键蛋白、主要生物过程和途径;其次,检测雌二醇(E2)、促卵泡激素(FSH)、促黄体生成素(LH)、孕酮(P)、Raf/ERK/ELK、HIF-1α/bFGF通路相关蛋白水平;最后通过代谢组学分析XZP对代谢产物的影响。结果与结论在本研究中,我们确定了XZP治疗HMG的关键靶点和通路,包括EGFR、VEGFA、ER和Ras信号通路。动物实验表明,XZP可降低HMG小鼠E2、LH、FSH水平,提高P的表达。XZP能恢复乳腺组织的正常结构,降低ERα、ERβ和PR的表达。此外,代谢组学结果显示XZP还调节HMG代谢产物,包括HIF-1α和代谢途径。Western blot结果显示,XZP干预可降低HMG小鼠乳腺组织中p-Raf1、Raf1、p-ERK1/2、ERK1/2、ELK、HIF-1α、bFGF蛋白的表达。XZP可能通过抑制细胞凋亡和血管生成来消除乳腺异常增生,这可能与调节HMG小鼠的Raf/ERK/ELK和HIF-1α/bFGF信号通路有关。这些结果提示XZP治疗可能有利于HMG的治疗。
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CiteScore
7.20
自引率
4.30%
发文量
567
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