Ultra-Performance Liquid Chromatography/Mass Spectrometry-Based Metabolomics for Discovering Potential Biomarkers and Metabolic Pathways of Colorectal Cancer in Mouse Model (ApcMin/ plus ) and Revealing the Effect of Honokiol

被引:6
作者
Chen, Xin [1 ,2 ]
Shi, Bo-lun [3 ]
Qi, Run-zhi
Chang, Xing [1 ,2 ]
Zheng, Hong-gang [1 ,3 ,4 ]
机构
[1] China Acad Chinese Med Sci, Guanganmen Hosp, Beijing, Peoples R China
[2] China Acad Chinese Med Sci, Beijing, Peoples R China
[3] China Acad Chinese Med Sci, Guanganmen Hosp, Dept Oncol, Beijing, Peoples R China
[4] Beijing Univ Chinese Med, Beijing, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
metabolomics; biomarkers; metabolites; ultra-performance liquid chromatography; mass spectrometry; BUTYRATE OXIDATION; KETONE-BODY; MECHANISMS; MICROBIOTA; RECEPTOR; CELLS;
D O I
10.3389/fonc.2021.671014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Endogenous metabolites are a class of molecules playing diverse and significant roles in many metabolic pathways for disease. Honokiol (HNK), an active poly-phenolic compound, has shown potent anticancer activities. However, the detailed crucial mechanism regulated by HNK in colorectal cancer remains unclear. In the present study, we investigated the therapeutic effects and the underlying molecular mechanisms of HNK on colorectal cancer in a mouse model (ApcMin/+) by analyzing the urine metabolic profile based on metabolomics, which is a powerful tool for characterizing metabolic disturbances. We found that potential urine biomarkers were involved in the metabolism of compounds such as purines, tyrosines, tryptophans, etc. Moreover, we showed that a total of 27 metabolites were the most contribution biomarkers for intestinal tumors, and we found that the citrate cycle (TCA cycle) was regulated by HNK. In addition, it was suggested that the efficacy of HNK was achieved by affecting the multi-pathway system via influencing relevant metabolic pathways and regulating metabolic function. Our work also showed that high-throughput metabolomics can characterize the regulation of metabolic disorders as a therapeutic strategy to prevent colorectal cancer.</p>
引用
收藏
页数:9
相关论文
共 50 条
[1]   Dietary fibre, whole grains, and risk of colorectal cancer: systematic review and dose-response meta-analysis of prospective studies [J].
Aune, Dagfinn ;
Chan, Doris S. M. ;
Lau, Rosa ;
Vieira, Rui ;
Greenwood, Darren C. ;
Kampman, Ellen ;
Norat, Teresa .
BMJ-BRITISH MEDICAL JOURNAL, 2011, 343 :1082
[2]   Honokiol for cancer therapeutics: A traditional medicine that can modulate multiple oncogenic targets [J].
Banik, Kishore ;
Ranaware, Abhishek Manoj ;
Deshpande, Vishwas ;
Nalawade, Savita Pravin ;
Padmavathi, Ganesan ;
Bordoloi, Devivasha ;
Sailo, Bethsebie Lalduhsaki ;
Shanmugam, Muthu K. ;
Fan, Lu ;
Arfuso, Frank ;
Sethi, Gautam ;
Kunnumakkar, Ajaikumar B. .
PHARMACOLOGICAL RESEARCH, 2019, 144 :192-209
[3]   STC2 promotes the epithelial-mesenchymal transition of colorectal cancer cells through AKT-ERK signaling pathways [J].
Chen, Bing ;
Zeng, Xiao ;
He, Yu ;
Wang, Xixi ;
Liang, Ziwei ;
Liu, Jingjing ;
Zhang, Peng ;
Zhu, Hongxia ;
Xu, Ningzhi ;
Liang, Shufang .
ONCOTARGET, 2016, 7 (44) :71400-71416
[4]   Ablating the aryl hydrocarbon receptor (AhR) in CD11c+cells perturbs intestinal epithelium development and intestinal immunity [J].
Chng, Song Hui ;
Kundu, Parag ;
Dominguez-Brauer, Carmen ;
Teo, Wei Ling ;
Kawajiri, Kaname ;
Fujii-Kuriyama, Yoshiaki ;
Mak, Tak Wah ;
Pettersson, Sven .
SCIENTIFIC REPORTS, 2016, 6
[5]   Host-Protozoan Interactions Protect from Mucosal Infections through Activation of the Inflammasome [J].
Chudnovskiy, Aleksey ;
Mortha, Arthur ;
Kana, Veronika ;
Kennard, Andrea ;
Ramirez, Juan David ;
Rahman, Adeeb ;
Remark, Romain ;
Mogno, Ilaria ;
Ng, Ruby ;
Gnjatic, Sasha ;
Amir, El-ad David ;
Solovyov, Alexander ;
Greenbaum, Benjamin ;
Clemente, Jose ;
Faith, Jeremiah ;
Belkaid, Yasmine ;
Grigg, Michael E. ;
Merad, Miriam .
CELL, 2016, 167 (02) :444-+
[6]   Impact of Exercise and Aging on Rat Urine and Blood Metabolome. An LC-MS Based Metabolomics Longitudinal Study [J].
Deda, Olga ;
Gika, Helen G. ;
Taitzoglou, Ioannis ;
Raikos, Nikolaos ;
Theodoridis, Georgios .
METABOLITES, 2017, 7 (01)
[7]   Interferon-β1a modulates glutamate neurotransmission in the CNS through CaMKII and GluN2A-containing NMDA receptors [J].
Di Filippo, Massimiliano ;
Tozzi, Alessandro ;
Arcangeli, Sara ;
de Iure, Antonio ;
Durante, Valentina ;
Di Gregorio, Maria ;
Gardoni, Fabrizio ;
Calabresi, Paolo .
NEUROPHARMACOLOGY, 2016, 100 :98-105
[8]   Targeting colorectal cancer-associated bacteria: A new area of research for personalized treatments [J].
Fais, T. ;
Delmas, J. ;
Cougnoux, A. ;
Dalmasso, G. ;
Bonnet, R. .
GUT MICROBES, 2016, 7 (04) :329-333
[9]   Gut microbiome development along the colorectal adenoma-carcinoma sequence [J].
Feng, Qiang ;
Liang, Suisha ;
Jia, Huijue ;
Stadlmayr, Andreas ;
Tang, Longqing ;
Lan, Zhou ;
Zhang, Dongya ;
Xia, Huihua ;
Xu, Xiaoying ;
Jie, Zhuye ;
Su, Lili ;
Li, Xiaoping ;
Li, Xin ;
Li, Junhua ;
Xiao, Liang ;
Huber-Schoenauer, Ursula ;
Niederseer, David ;
Xu, Xun ;
Al-Aama, Jumana Yousuf ;
Yang, Huanming ;
Wang, Jian ;
Kristiansen, Karsten ;
Arumugam, Manimozhiyan ;
Tilg, Herbert ;
Datz, Christian ;
Wang, Jun .
NATURE COMMUNICATIONS, 2015, 6
[10]   Glutamate dependent NMDA receptor 2D is a novel angiogenic tumour endothelial marker in colorectal cancer [J].
Ferguson, Henry J. M. ;
Wragg, Joseph W. ;
Ward, Stephen ;
Heath, Victoria L. ;
Ismail, Tariq ;
Bicknell, Roy .
ONCOTARGET, 2016, 7 (15) :20440-20454