Schisantherin A inhibits cell proliferation by regulating glucose metabolism pathway in hepatocellular carcinoma

被引:5
作者
Feng, Fan [1 ]
Pan, Lianhong [2 ]
Wu, Jiaqin [1 ]
Liu, Mingying [3 ]
He, Long [4 ]
Yang, Li [1 ]
Zhou, Wei [5 ]
机构
[1] Chongqing Univ, Coll Bioengn, Key Lab Biorheol Sci & Technol, Natl Innovat & Attracting Talents 111 Base,Minist, Chongqing, Peoples R China
[2] Chongqing Three Gorges Med Coll, Chongqing Engn Res Ctr Antitumor Nat Drugs, Chongqing, Peoples R China
[3] XiHua Univ, Sch Comprehens Hlth Management, Chengdu, Sichuan, Peoples R China
[4] Chongqing Univ Educ, Sch Artificial Intelligence, Chongqing, Peoples R China
[5] Chongqing Univ, Chongqing Key Lab Translat Res Canc Metastasis & I, Canc Hosp, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
schisantherin A; hepatocellular carcinoma; fructose and pentose phosphate metabolism; galactose metabolism; traditional Chinese medicine; GLYCOLYSIS; EXPRESSION; DIAGNOSIS; PROGRESS; CANCER;
D O I
10.3389/fphar.2022.1019486
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Schisantherin A (STA) is a traditional Chinese medicine extracted from the plant Schisandra chinensis, which has a wide range of anti-inflammatory, antioxidant, and other pharmacological effects. This study investigates the anti-hepatocellular carcinoma effects of STA and the underlying mechanisms. STA significantly inhibits the proliferation and migration of Hep3B and HCCLM3 cells in vitro in a concentration-dependent manner. RNA-sequencing showed that 77 genes are upregulated and 136 genes are downregulated in STA-treated cells compared with untreated cells. KEGG pathway analysis showed significant enrichment in galactose metabolism as well as in fructose and mannose metabolism. Further gas chromatography-mass spectrometric analysis (GC-MS) confirmed this, indicating that STA significantly inhibits the glucose metabolism pathway of Hep3B cells. Tumor xenograft in nude mice showed that STA has a significant inhibitory effect on tumor growth in vivo. In conclusion, our results indicate that STA can inhibit cell proliferation by regulating glucose metabolism, with subsequent anti-tumor effects, and has the potential to be a candidate drug for the treatment of liver cancer.
引用
收藏
页数:12
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