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疏肝化症方治疗三阴性乳腺癌:基于网络药理学和体内实验的研究

The Shuganhuazheng Formula in Triple-Negative Breast Cancer: A Study Based on Network Pharmacology and In Vivo Experiments.

作者信息

Wang Bo, Fei Rui, Yang Yan, Jing Niancai, Lu Yi, Xiao Hongyu, Yang Jili, Zhang Yue

机构信息

Changchun University of Chinese Medicine, Changchun, Jilin 130117, China.

Cell Biology Department, School of Basic Medicine, Jilin University, Changchun, Jilin 130021, China.

出版信息

Evid Based Complement Alternat Med. 2020 Dec 14;2020:8173147. doi: 10.1155/2020/8173147. eCollection 2020.

Abstract

Breast cancer is the most common cancer in women. Among breast cancer subtypes, triple-negative breast cancer (TNBC) has the highest degree of malignancy and the worst prognosis. The Shuganhuazheng formula (SGHZF) is a traditional Chinese herbal formula for the treatment of TNBC, but the mechanism of SGHZF in the treatment of TNBC remains unclear. In this study, the therapeutic effect and mechanism of SGHZF against TNBC were preliminarily determined based on in vivo experimental verification and network pharmacology. In terms of therapeutic effects, the antitumour effect was verified by measuring and calculating tumour volume, and the expression of proto-oncogene c-Myc was verified by PCR. In terms of the mechanism, potential therapeutic targets were identified by overlapping the SGHZF-related and TNBC-related targets. After comprehensively analysing the results of the protein-protein interaction (PPI), gene ontology (GO) function, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses, Akt and HIF-1 were selected for verification by using immunohistochemical and Western blot analyses. The results of the study indicated that SGHZF can inhibit breast tumour growth in mice and that the mechanism may be related to the inhibition of Akt and HIF-1 expression.

摘要

乳腺癌是女性中最常见的癌症。在乳腺癌亚型中,三阴性乳腺癌(TNBC)恶性程度最高,预后最差。疏肝化症方(SGHZF)是一种用于治疗TNBC的传统中药方剂,但SGHZF治疗TNBC的机制尚不清楚。在本研究中,基于体内实验验证和网络药理学初步确定了SGHZF抗TNBC的治疗效果和机制。在治疗效果方面,通过测量和计算肿瘤体积来验证抗肿瘤作用,并通过PCR验证原癌基因c-Myc的表达。在机制方面,通过重叠SGHZF相关靶点和TNBC相关靶点来确定潜在的治疗靶点。在综合分析蛋白质-蛋白质相互作用(PPI)、基因本体(GO)功能和京都基因与基因组百科全书(KEGG)通路富集分析的结果后,选择Akt和HIF-1通过免疫组织化学和蛋白质印迹分析进行验证。研究结果表明,SGHZF可以抑制小鼠乳腺肿瘤生长,其机制可能与抑制Akt和HIF-1表达有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ae3/7752265/7e535bd933c9/ECAM2020-8173147.001.jpg

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