Metabolic Profiling of Amino Acids by Liquid Chromatography-Tandem Mass Spectrometry (LC-MS) to Characterize the Significance of Glutamine in Triple-Negative Breast Cancer (TNBC)

被引:0
作者
Chen, Xiaowu [1 ,2 ,3 ]
Gao, Dan [2 ,4 ]
Sun, Qinsheng [4 ]
Chen, Yuzong [2 ,4 ]
Liu, Hongxia [2 ,3 ]
Jiang, Yuyang [1 ,4 ]
机构
[1] Shenyang Pharmaceut Univ, Shenyang, Liaoning, Peoples R China
[2] Shenzhen Kivita Innovat Drug Discovery Inst, Analyt & Testing Ctr, Shenzhen, Peoples R China
[3] Tsinghua Univ, Grad Sch Shenzhen, Key Lab Metabol Shenzhen, Shenzhen, Peoples R China
[4] Tsinghua Univ, Grad Sch Shenzhen, Shenzhen Key Lab Chem Biol, State Key Lab Breeding Base, Shenzhen, Peoples R China
关键词
Amino acids; biomarker; glutamine; liquid chromatography-tandem mass spectrometry; triple-negative breast cancer; ARGININE DEIMINASE; THERAPY; TRANSFORMATION; SURVIVAL; TARGETS; PROTEIN; GROWTH; CELLS;
D O I
10.1080/00032719.2018.1513021
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Triple-negative breast cancer (TNBC) is considered to be aggressive based on its low overall survival and disease-free rates. Currently, there is no molecular-targeted therapy. The identification of a suitable biomarker is still a research focus for TNBC at the present time. Amino acid metabolism fulfills multiple important physiological roles in humans. Their metabolic abnormalities have been reported in numerous cancer studies and amino acid pathways may also be chemotherapeutic targets. This study reports the profiling analysis of amino acids in TNBC and non-TNBC cell lines for detecting biomarkers based on the strategy of N-phosphorylation labeling with liquid chromatography-tandem mass spectrometry (LC-MS). Glutamine (Gln) was found to be significantly down-regulated in TNBC cells because it was largely absorbed and consumed in the TNBC cell lines. These results indicate faster proliferation of TNBC and higher consumption of glutamine to meet the material and energy demand, suggesting its potential role in TNBC progression. Hence, glutamine may be regarded as a biomarker and Gln-targeted approaches may become a new therapeutic strategies for TNBC.
引用
收藏
页码:1068 / 1082
页数:15
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