Metformin suppressed the proliferation of LoVo cells and induced a time-dependent metabolic and transcriptional alteration

被引:34
作者
He, Jiaojiao [1 ]
Wang, Ke [3 ]
Zheng, Ningning [1 ]
Qiu, Yunping [6 ]
Xie, Guoxiang [7 ]
Su, Mingming [7 ]
Jia, Wei [1 ,4 ,5 ,7 ]
Li, Houkai [1 ,2 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Ctr Chinese Med Therapy & Syst Biol, Shanghai 201203, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Sch Publ Hlth, Shanghai 201203, Peoples R China
[3] Shanghai Univ Tradit Chinese Med, Shuguang Hosp, Lab Integrat Med Surg, Shanghai 201203, Peoples R China
[4] Shanghai Jiao Tong Univ, Peoples Hosp 6, Ctr Translat Med, Shanghai 200233, Peoples R China
[5] Shanghai Jiao Tong Univ, Peoples Hosp 6, Dept Endocrinol & Metab, Shanghai Key Lab Diabet Mellitus, Shanghai 200233, Peoples R China
[6] Albert Einstein Coll Med, Ctr Diabet, Stable Isotope & Metabol Core Facil, Bronx, NY 10461 USA
[7] Univ Hawaii, Ctr Canc, Canc Epidemiol Program, Honolulu, HI 96813 USA
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
关键词
COLORECTAL-CANCER; GROWTH; SENSITIZATION; CYTOTOXICITY; INHIBITION; INCREASES; THERAPY; REVEALS; RISK;
D O I
10.1038/srep17423
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Metformin is a widely used anti-diabetic drug with potential anti-tumor activity. However, little is known about its global metabolic and transcriptional impacts on tumor cells. In current study, we performed a metabolic profiling on human-derived colon cancer LoVo cells treated by 10 mM metformin for 8, 24 and 48 h. An obvious time-dependent metabolic alteration was observed from 8 to 48 h, prior to the reduction of cell viability. A total of 47, 45 and 66 differential metabolites were identified between control and metformin-treated cells at three time points. Most of the metabolites were up-regulated at 8 h, but down-regulated at 24 and 48 h by metformin. These metabolites were mainly involved in carbohydrates, lipids, amino acids, vitamins and nucleotides metabolism pathways. Meanwhile, the transcirptomic profile revealed 134 and 3061 differentially expressed genes at 8 and 24 h by metformin. In addition to the cancer signaling pathways, expression of genes involved in cell energy metabolism pathways was significantly altered, which were further validated with genes in glucose metabolism pathway. Altogether, our current data indicate that metformin suppressed the proliferation of LoVo cells, which may be due to the modulation on cell energy metabolism at both metabolic and transcriptional levels in a time-dependent way.
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页数:16
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