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Metabolomic Study on Nude Mice Models of Gastric Cancer Treated with Modified Si Jun Zi Tang via HILIC UHPLC-Q-TOF/MS Analysis

机译:通过HILIC UHPLC-Q-TOF / MS分析治疗胃癌裸鼠裸鼠裸鼠裸鼠裸鼠模型的代谢组研究

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Recently, metabolomic methods have been used to explore the complex pathogenesis of cancer and the mechanism of action of traditional Chinese medicine (TCM) formulae. In this study, first, modified Si Jun Zi Tang (MSJZT) was prepared with strict quality control using the instrument method of ultra performance liquid chromatography and photodiode array detector (UPLC-PDA). Subsequently, in vivo experiments with tumour-bearing nude mice demonstrated that MSJZT exerted good antitumour effects. MSJZT not only significantly increased mouse body weight but also shrank the tumour volume. Then, the HILIC UHPLC-Q-TOF/MS-based metabolomics approach was used for exploring the pathogenesis of gastric cancer and the molecular mechanism of MSJZT. A total of 59 potential biomarkers in plasma were identified, and 6 pathways were found to be disturbed in gastric cancer. In contrast, after 3 weeks of MSJZT intervention, 32 potential biomarkers were identified, and 4 altered pathways were detected. The changes in glycolytic, amino acid, and lipid metabolisms could be partially regulated by MSJZT through decreasing the content of lactic dehydrogenase (LDH), glutamine synthetase (GS), phosphocholine cytidylyltransferase (PCYT2) mRNA, and protein level. In conclusion, we established a HILIC UHPLC-Q-TOF/MS metabolomic analysis method to demonstrate a complex metabolic profile of gastric cancer. The disordered metabolism could be partially regulated by MSJZT. These findings not only establish a solid foundation for TCM to treat gastric cancer but also provide a basis for further exploration of the precise mechanism of MSJZT activity.
机译:最近,代谢物方法已被用于探讨癌症的复杂发病机制和中药(TCM)公式的作用机制。在本研究中,首先,使用超级性能液相色谱和光电二极管阵列检测器(UPLC-PDA)的仪器方法,使用严格的质量控制来制备改性Si Jun Zi汤(MSJZT)。随后,在体内携带肿瘤裸鼠的实验中表明MSJZT施加了良好的抗肿瘤效果。 MSJZT不仅显着增加了小鼠体重,而且缩小了肿瘤体积。然后,用于探索胃癌的发病机制和MSJZT的分子机制的HILIC UHPLC-Q-TOF / MS基于MSJZT的发病机制。鉴定了总共59个潜在的生物标志物,发现6种途径在胃癌中受到干扰。相反,在3周的MSJZT干预后,鉴定了32个潜在的生物标志物,检测到4个潜在的途径。通过降低乳酸脱氢酶(LDH),谷氨酰胺合成酶(GS),普华氨酸细胞裂解性转移酶(PCYT2)mRNA和蛋白质水平的糖醇类,氨基酸和脂质代谢的变化可以通过MSJZT进行部分调节。总之,我们建立了一种HILIC UHPLC-Q-TOF / MS代谢物分析方法,以证明胃癌的复杂代谢型材。无序的代谢可以由MSJZT部分调节。这些发现不仅为TCM治疗胃癌而建立了坚实的基础,还为进一步探索MSJZT活动的确切机制提供了依据。

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