作者: Wenchen Li , Hongmei Jia , Qi Li , Jiayue Cui , Ri Li
DOI: 10.1038/S41598-018-32847-8
关键词: Glioma 、 Chemistry 、 Regulation of gene expression 、 Metabolomics 、 Metabolome 、 Nucleotidase 、 Gene expression 、 Inositol monophosphatase 、 Metabolic pathway 、 Cancer research
摘要: Glioma is the most prevalent malignant brain tumor. A comprehensive analysis of glioma metabolome still lacking. This study aims to explore new special metabolites in tissues. non-targeted human metabolomics was performed by UPLC-Q-TOF/MS. The gene expressions 18 enzymes associated with 3’-phosphoadenylate (pAp) metabolism examined qRT-PCR. Those cover primary metabolic pathway pAp. We identified 15 (13 lipids and 2 nucleotides) that were significantly different between control Glycerophosphatidylcholine [PC(36:1)] content high pAp low (p < 0.01). In tissues, PC(36:1) not detected increased. 3′-nucleotidases (Inositol monophosphatase (IMPAD-1) 3′(2′),5′-bisphosphate nucleotidase 1(BPNT-1)) dramatically down-regulated. Meanwhile, expression 8 sulfotransferases (SULT), phosphoadenosine phosphosulfate synthases (PAPSS-1 PAPSS-2) L-aminoadipate-semialdehyde dehydrogenase-phosphopante-theinyl transferase (AASDHPPT) up-regulated. absence accumulation are noticeable aberration glioma. dramatic down-regulation IMPAD-1 BPNT-1 cause for accumulation. Our findings suggest differential discovered could be used as potentially novel therapeutic targets or diagnostic biomarkers abnormal nucleotides play roles pathogenesis