National Chinmedomics Research Center, Sino-America Chinmedomics Technology Collaboration Center, National TCM Key Laboratory of Serum Pharmacochemistry, Laboratory of Metabolomics, Department of Pharmaceutical Analysis, Heilongjiang University of Chinese Medicine, Heping Road 24, Harbin, China.
State Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Avenida Wai Long, Taipa, Macau.
J Proteomics. 2019 Aug 30;206:103447. doi: 10.1016/j.jprot.2019.103447. Epub 2019 Jul 19.
Functional metabolomics could bring correlative information about specific cell types under different conditions for exploring cell properties and functions. In this study, we adopt a non-targeted cell metabolomics strategy to reveal the proliferation inhibition mechanism of obacunone on 22RV1 prostate cancer cells. Using high-throughput liquid chromatography-high definition mass spectrometry combined with pattern recognition methods was performed to analyze the cell metabolic profiles and pathway of obacunone on prostate cancer. A total of twenty one proposed metabolites in prostate cancer cell and nine vital metabolic pathways such as nicotinate and nicotinamide metabolism, phenylalanine metabolism as well as tryptophan metabolism were identified from large amounts of data. Then, we have built an overall metabolic description network of obacunone to defense prostate cancer. In addition, morphological observation, cell proliferation and apoptosis analysis of 22RV1 human prostate cancer cells were performed to better understand physiopathologic changes after obacunone treatment. Functional metabolomics is a valuable tool that insight into the natural product mechanisms and contributes to new drug discovery. SIGNIFICANCE: In this study, we probe into the proliferation inhibition effect of obacunone on 22RV1 prostate cancer cells by differentiating metabolic changes of cell sample in control and obacunone administration. Using the non-targeted and targeted cell metabolomics approaches, our findings were manifested that obacunone effectually control proliferation and promote apoptosis in 22RV1 prostate cancer cells, which were related to twenty one proposed metabolites, and nicotinate and nicotinamide metabolism, phenylalanine metabolism, tryptophan metabolism as well as ascorbate metabolism. These data were suggested that functional metabolomics analysis have potential to explore the pharmacodynamic mechanism through resolving metabolic changes in cancer cells that possesses higher clinical application value. The advances in the molecular understanding of the roles of metabolomic pathway concerned with particular metabolites in obacunone administration attract more attention in favor of burgeoning therapeutic measures resisting prostate cancer.
功能代谢组学可以提供关于不同条件下特定细胞类型的相关信息,以探索细胞特性和功能。在这项研究中,我们采用非靶向细胞代谢组学策略来揭示obacunone 对 22RV1 前列腺癌细胞增殖抑制的机制。使用高通量液相色谱-高分辨率质谱结合模式识别方法分析obacunone 对前列腺癌细胞的代谢谱和途径。从大量数据中鉴定出前列腺癌细胞中的 21 种提出的代谢物和 9 种重要的代谢途径,如烟酸和烟酰胺代谢、苯丙氨酸代谢以及色氨酸代谢。然后,我们构建了obacunone 防御前列腺癌的整体代谢描述网络。此外,还对 22RV1 人前列腺癌细胞进行形态观察、细胞增殖和凋亡分析,以更好地了解obacunone 处理后的生理病理变化。功能代谢组学是一种有价值的工具,可以深入了解天然产物的作用机制,并有助于新药的发现。意义:在这项研究中,我们通过区分对照和obacunone 给药的细胞样本的代谢变化,探究了obacunone 对 22RV1 前列腺癌细胞增殖的抑制作用。使用非靶向和靶向细胞代谢组学方法,我们的研究结果表明,obacunone 有效控制 22RV1 前列腺癌细胞的增殖并促进其凋亡,这与 21 种提出的代谢物以及烟酸和烟酰胺代谢、苯丙氨酸代谢、色氨酸代谢和抗坏血酸代谢有关。这些数据表明,功能代谢组学分析通过解析癌细胞中的代谢变化,有潜力探索药效学机制,具有更高的临床应用价值。代谢途径中特定代谢物在obacunone 给药中的分子作用的深入理解引起了更多的关注,有利于新兴的治疗前列腺癌的措施。