Insights into the Molecular Mechanisms of Bushen Huoxue Decoction in Breast Cancer via Network Pharmacology and in vitro experiments

IF 1.5 4区 医学 Q4 CHEMISTRY, MEDICINAL
Hongyi Liang, Guoliang Yin, Guangxi Shi, Xiaofei Liu, Zhiyong Liu, Jingwei Li
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引用次数: 0

Abstract

Aim:: Breast cancer (BC) is by far seen as the most common malignancy globally, with 2.261 million patients newly diagnosed, accounting for 11.7% of all cancer patients, according to the Global Cancer Statistics Report (2020). The luminal A subtype accounts for at least half of all BC diagnoses. According to TCM theory, Bushen Huoxue Decoction (BSHXD) is a prescription used for cancer treatment that may influence luminal A subtype breast cancer (LASBC). Objectives:: To analyze the clinical efficacy and underlying mechanisms of BSHXD in LASBC. Materials and Methods:: Network pharmacology and in vitro experiments were utilized to foresee the underlying mechanism of BSHXD for LASBC. Results:: According to the bioinformatics analysis, BSHXD induced several proliferation and apoptosis processes against LASBC, and the presumed targets of active components in BSHXD were mainly enriched in the HIF-1 and PI3K/AKT pathways. Flow cytometry assay and western blotting results revealed that the rate of apoptosis enhanced in a dose-dependent manner with BSHXD concentration increasing, respectively. BSHXD notably downregulated the expressions of HIF-1α, P-PI3K, PI3K, P-AKT and AKT proteins. However, adding an HIF-1α agonist restored those protein levels. Conclusion:: The study proved that the mechanism of BSHXD in LASBC may be connected to suppressing proliferation by inhibiting the activity of the HIF-1α/PI3K/AKT signaling pathway and promoting apoptosis via the Caspase cascade in LASBC cells.
网络药理学及体外实验探讨补肾活血汤治疗乳腺癌的分子机制
目的:根据《全球癌症统计报告(2020)》,乳腺癌(BC)是迄今为止全球最常见的恶性肿瘤,新确诊患者226.1万例,占所有癌症患者的11.7%。腔内A亚型至少占所有BC诊断的一半。根据中医理论,补肾活血汤(BSHXD)是一种用于癌症治疗的方剂,可能影响腔内a亚型乳腺癌(LASBC)。目的:分析BSHXD治疗LASBC的临床疗效及机制。材料与方法:采用网络药理学和体外实验方法,探讨白芍散治疗LASBC的作用机制。结果:生物信息学分析表明,BSHXD可诱导LASBC的多种增殖和凋亡过程,推测BSHXD的活性成分主要富集于HIF-1和PI3K/AKT通路。流式细胞术和western blotting结果显示,BSHXD浓度升高,细胞凋亡率呈剂量依赖性增强。BSHXD显著下调HIF-1α、P-PI3K、PI3K、P-AKT和AKT蛋白的表达。然而,添加HIF-1α激动剂可以恢复这些蛋白水平。结论:本研究证实BSHXD在LASBC中的作用机制可能通过抑制HIF-1α/PI3K/AKT信号通路活性,通过Caspase级联促进LASBC细胞凋亡,从而抑制LASBC细胞增殖。
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来源期刊
Current computer-aided drug design
Current computer-aided drug design 医学-计算机:跨学科应用
CiteScore
3.70
自引率
5.90%
发文量
46
审稿时长
>12 weeks
期刊介绍: Aims & Scope Current Computer-Aided Drug Design aims to publish all the latest developments in drug design based on computational techniques. The field of computer-aided drug design has had extensive impact in the area of drug design. Current Computer-Aided Drug Design is an essential journal for all medicinal chemists who wish to be kept informed and up-to-date with all the latest and important developments in computer-aided methodologies and their applications in drug discovery. Each issue contains a series of timely, in-depth reviews, original research articles and letter articles written by leaders in the field, covering a range of computational techniques for drug design, screening, ADME studies, theoretical chemistry; computational chemistry; computer and molecular graphics; molecular modeling; protein engineering; drug design; expert systems; general structure-property relationships; molecular dynamics; chemical database development and usage etc., providing excellent rationales for drug development.
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