Uncovering the anticancer mechanism of petroleum extracts of Farfarae Flos against Lewis lung cancer by metabolomics and network pharmacology analysis

被引:15
作者
Yu, Shuting [1 ,2 ]
Li, Jing [3 ]
Gao, Wei [4 ]
Wu, Yongyan [4 ]
Qin, Xuemei [1 ]
Li, Zhenyu [1 ]
机构
[1] Shanxi Univ, Modern Res Ctr Tradit Chinese Med, 92 Wucheng Rd, Taiyuan 030006, Shanxi, Peoples R China
[2] Shanxi Univ, Coll Chem & Chem Engn, Taiyuan, Shanxi, Peoples R China
[3] Wuhan Univ Sch Pharmaceut Sci, Key Lab Combinatorial Biosynth & Drug Discovery, Minist Educ, Wuhan, Hubei, Peoples R China
[4] Shanxi Med Univ, Hosp 1, Dept Otolaryngol Head & Neck Surg, Shanxi Key Lab Otorhinolaryngol Head & Neck Canc, Taiyuan, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
cellular uptake compounds; Farfarae Flos; Lewis lung cancer cells; metabolomics; network pharmacology; IDENTIFICATION; METAANALYSIS;
D O I
10.1002/bmc.4878
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Lung cancer shows the highest incidence rate in the world. Thus, it has become increasingly important to find therapeutic drugs to treat lung cancer. Farfarae Flos (FF) has been used in traditional Chinese medicine to treat pulmonary diseases such as cough, bronchitis and asthmatic disorders. In this study, the anti-proliferation effects of petroleum extracts of FF (PEFF) on Lewis lung cancer cells and the corresponding mechanisms were studied using cell metabolomics. Fifteen differential metabolites in the cell extracts and the corresponding medium related to the anti-proliferation effect of PEFF were identified, which were probably involved in pyruvate metabolism and glycine, serine and threonine metabolism. For the cellular uptake compounds in PEFF, six metabolites derived from two prototype compounds were also tentatively identified by UHPLC-Q-Orbitrap high-resolution MS. Network pharmacology analysis demonstrated that the anti-proliferation mechanism of PEFF was also probably related to the target genes, including, Aurora-A, glutathione S-transferase Mu 1 (GSTM1), glutathione S-transferase P 1 (GSTP1), progesterone receptor and heme oxygenase-1 (HO-1), and further associated with the proteoglycans and PI3K/Akt signaling pathway. Cell metabolomics and network pharmacology analysis provided a holistic method to investigate the anti-proliferation mechanisms of PEFF. However, further studies were still needed to validate the potential target genes, pathways and active compounds in PEFF.
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页数:12
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