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引用次数: 0
摘要
胶质瘤是一种错综复杂的肿瘤,其代谢和遗传异常导致了其侵袭性表型和不良预后。本研究旨在确定可用于区分不同等级胶质瘤的关键分子代谢和基因表达变异,从而更深入地了解胶质瘤的代谢状况,为将来的诊断提供依据。本研究对胶质瘤活检样本(n = 52;患者包括良性和恶性病变)进行了代谢组学分析以及临床和表达分析。利用 RT-PCR 和 Western 印迹技术对活检组织进行了基因/蛋白质表达分析,并进行了代谢物分析。基因/蛋白表达分析的结果显示,与对照组相比,高级别胶质瘤中的肉碱棕榈酰基转移酶、单甘酯脂肪酶、人磷酸果糖激酶和异柠檬酸脱氢酶水平升高。我们的研究表明,代谢物和基因/蛋白质表达水平对不同等级的胶质瘤具有鉴别作用。这项研究为我们提供了更深入的见解,这些见解对于采用专门针对失调代谢组的差异化治疗方法至关重要,从而使患者受益。
Targeted Metabolic Profiling in Determining the Metabolic Heterogeneity in Human Biopsies of Different Grades of Glioma.
Gliomas are intricate tumors with numerous metabolic and genetic abnormalities contributing to their aggressive phenotypes and poor prognoses. The study aims at identifying the key molecular metabolic as well as gene expressional variations that could be used to differentiate between different grades of glioma to obtain deeper insights the about metabolic status of glioma that may serve as good candidates of diagnosis in future. In the present study, the metabolomic profiling along with clinical and expressional analyses of glioma biopsies (n = 52; patients comprising both of benign and malignant lesions) was analyzed. The biopsies were subjected to gene/protein expressional analysis using RT-PCR and western blotting and also were subjected to metabolite analyses. The results of the gene/protein expressional analysis exhibited elevated levels of carnitine palmitoyltransferase, monoglyceride lipase, human phosphofructokinase, and isocitrate dehydrogenase in higher grades of glioma when compared to those of control. Our study suggested that the metabolites and gene/protein expressional levels were found to be discriminative among the grades of glioma. The study is deemed as a provider of deeper insights that are essential for differential therapeutic approaches that specifically target the dysregulated metabolome to the benefit of patients.
期刊介绍:
Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.