Metabolic switching in the hypoglycemic and antitumor effects of metformin on high glucose induced HepG2 cells

被引:21
|
作者
Lv, Yan [1 ,2 ]
Tian, Na [1 ,2 ]
Wang, Junsong [3 ]
Yang, Minghua [1 ,2 ]
Kong, Lingyi [1 ,2 ]
机构
[1] China Pharmaceut Univ, Dept Nat Med Chem, Jiangsu Key Lab Bioact Nat Prod Res, 24 Tong Jia Xiang, Nanjing 210009, Jiangsu, Peoples R China
[2] China Pharmaceut Univ, Dept Nat Med Chem, State Key Lab Nat Med, 24 Tong Jia Xiang, Nanjing 210009, Jiangsu, Peoples R China
[3] Nanjing Univ Sci & Technol, Ctr Mol Metab, Sch Environm & Biol Engn, Xiao Ling Wei 200, Nanjing 210094, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Metformin; NMR; Metabolomics; Insulin resistance; Hypoglycemic; Anticancer; BREAST-CANCER; REDUCED RISK; NORMALIZATION; ASSOCIATION;
D O I
10.1016/j.jpba.2018.04.029
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Metformin, a widely prescribed drug for the management of type 2 diabetes mellitus, has potential anticancer effect. Diabetes patients regularly taking metformin have been reported with decreased cancer risk and improved cancer prognosis in recent years. A cell model of high glucose induced HepG2 cells was conducted to mimic insulin resistance, and a H-1 NMR-based metabolomics approach in conjunction with molecular biology was performed to investigate the metabolic changes of high glucose induced HepG2 cells in response to different doses of metformin treatment and to study the differences and links between hypoglycemic and antitumor effects of metformin. Metformin with hypoglycemic effect rectified glucose metabolic imbalance and regulated oxidative stress, energy and amino acid metabolism. Metformin inhibited tumor cell proliferation and induced apoptosis through activation of AMPK/mTOR pathway and further influencing energy metabolism, phospholipid metabolism and glucose catabolism. The integrated metabolomics approach showed its potential in clarifying the different action on metformin treatment and understanding the pleiotropic effect of metformin. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:153 / 162
页数:10
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