Integrated Metabolomics and Lipidomics Analyses Reveal Metabolic Reprogramming in Human Glioma with IDH1 Mutation
Xu, Guowang1; Zhou, Lina1; Wang, Zhichao1,2; Hu, Chunxiu1; Zhang, Chaoqi3; Kovatcheva-Datchary, Petia1; Yu, Di1,2; Liu, Shasha3; Ren, Feifei3; Wang, Xiaolin1
刊名JOURNAL OF PROTEOME RESEARCH
2019-03-01
卷号18期号:3页码:960-969
关键词glioma IDH1 metabolomics lipidomics metabolic reprogramming
ISSN号1535-3893
DOI10.1021/acs.jproteome.8b00663
通讯作者Zhang, Yi(yizhang@zzu.edu.cn) ; Xu, Guowang()
英文摘要Mutations in isocitrate dehydrogenase (IDH) 1 are high-frequency events in low-grade glioma and secondary glioblastoma, and IDH1 mutant gliomas are vulnerable to interventions. Metabolic reprogramming is a hallmark of cancer. In this study, comprehensive metabolism investigation of clinical IDH1 mutant glioma specimens was performed to explore its specific metabolic reprogramming in real micro environment. Massive metabolic alterations from glycolysis to lipid metabolism were identified in the IDH1 mutant glioma tissue when compared to IDH1 wild-type glioma. Of note, tricarboxylic acid (TCA) cycle intermediates were in similar levels in both groups, with more pyruvate found entering the TCA cycle in IDH1 mutant glioma. The pool of fatty acyl chains was also reduced, displayed as decreased triglycerides and sphingolipids, although membrane phosphatidyl lipids were not changed. The lower fatty acyl pool may be mediated by the lower protein expression levels of long-chain acyl-CoA synthetase 1 (ACSL1), ACSL4, and very long-chain acyl-CoA synthetase 3 (ACSVL3) in IDH1 mutant glioma. Lower ACSL1 was further found to contribute to the better survival of IDH1 mutant glioma patients based on the The Cancer Genome Atlas (TCGA) RNA sequencing data. Our research provides valuable insights into the tissue metabolism of human IDH1 mutant glioma and unravels new lipid-related targets.
资助项目National Natural Science Foundation of China[81472374] ; National Natural Science Foundation of China[21505132] ; National Natural Science Foundation of China[21435006] ; [2017YFC0906900]
WOS关键词ISOCITRATE DEHYDROGENASE 1 ; OXIDATIVE STRESS ; R132H MUTATION ; CANCER ; PROFILES ; GROWTH ; CELLS
WOS研究方向Biochemistry & Molecular Biology
语种英语
出版者AMER CHEMICAL SOC
WOS记录号WOS:000460491800014
资助机构National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China
内容类型期刊论文
源URL[http://cas-ir.dicp.ac.cn/handle/321008/165894]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
通讯作者Xu, Guowang; Zhang, Yi
作者单位1.Chinese Acad Sci, Dalian Inst Chem Phys, CAS Key Lab Separat Sci Analyt Chem, Dalian 116023, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
3.Zhengzhou Univ, Affiliated Hosp 1, Biotherapy Ctr, Zhengzhou 450052, Henan, Peoples R China
推荐引用方式
GB/T 7714
Xu, Guowang,Zhou, Lina,Wang, Zhichao,et al. Integrated Metabolomics and Lipidomics Analyses Reveal Metabolic Reprogramming in Human Glioma with IDH1 Mutation[J]. JOURNAL OF PROTEOME RESEARCH,2019,18(3):960-969.
APA Xu, Guowang.,Zhou, Lina.,Wang, Zhichao.,Hu, Chunxiu.,Zhang, Chaoqi.,...&Zhang, Yi.(2019).Integrated Metabolomics and Lipidomics Analyses Reveal Metabolic Reprogramming in Human Glioma with IDH1 Mutation.JOURNAL OF PROTEOME RESEARCH,18(3),960-969.
MLA Xu, Guowang,et al."Integrated Metabolomics and Lipidomics Analyses Reveal Metabolic Reprogramming in Human Glioma with IDH1 Mutation".JOURNAL OF PROTEOME RESEARCH 18.3(2019):960-969.
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