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

IF 1.5 4区 医学 Q4 CHEMISTRY, MEDICINAL Current computer-aided drug design Pub Date : 2023-12-01 DOI:10.2174/0115734099269728231115060827
Hongyi Liang, Guoliang Yin, Guangxi Shi, Xiaofei Liu, Zhiyong Liu, Jingwei Li
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引用次数: 0

摘要

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