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颅内肿瘤的31P核磁共振磷脂质特征分析

31P NMR phospholipid characterization of intracranial tumors.

作者信息

Merchant T E, van der Ven L T, Minsky B D, Diamantis P M, Delapaz R, Galicich J, Glonek T

机构信息

Department of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021.

出版信息

Brain Res. 1994 Jun 27;649(1-2):1-6. doi: 10.1016/0006-8993(94)91041-3.

DOI:10.1016/0006-8993(94)91041-3
PMID:7953620
Abstract

Phospholipid extracts from 48 intracranial tumors were analyzed using 31P NMR. Phospholipids commonly identified in the tumor spectra included phosphatidylglycerol (PG), phosphatidic acid (PA), diphosphatidylglycerol (DPG), uncharacterized phospholipid (U), ethanolamine plasmalogen (EPLAS), phosphatidylethanolamine (PE), phosphatidylserine (PS), sphingomyelin (SM), lysophosphatidylcholine (LPC), phosphatidylinositol (PI), a choline phospholipid (CPLIP), and phosphatidylcholine (PC). Differences in the mean relative mole-percentage of phosphorus concentrations of individual phospholipids were used to differentiate among tumors. Neural sheath tumors (neurilemmoma, neurofibroma and fibrosarcoma) were noted to contain significantly elevated levels of SM relative to tumors of neural glial origin and individually, glioblastoma multiforme was noted to contain depressed levels of SM relative to neurilemmoma, neurofibroma and meningioma. Significantly decreased levels of PA were noted for glioblastoma relative to neurilemmoma along with significantly decreased levels of PE relative to meningioma. Elevated levels of LPC and CPLIP were seen in glioblastoma multiforme relative to meningioma. Additional findings included elevated levels of PC for glioblastoma multiforme relative to neurofibroma, and neurilemmoma was differentiated from neurofibroma with elevated levels of PA and depressed levels of PI. 31P NMR phospholipid analysis provides supplemental biochemical information which may be used to improve the interpretation of spectra acquired in vivo, and reveals important tumor-specific biochemical information which may further improve the understanding of the biological behavior of intracranial tumors.

摘要

使用31P核磁共振对48个颅内肿瘤的磷脂提取物进行了分析。在肿瘤光谱中常见的磷脂包括磷脂酰甘油(PG)、磷脂酸(PA)、二磷脂酰甘油(DPG)、未鉴定的磷脂(U)乙醇胺缩醛磷脂(EPLAS)、磷脂酰乙醇胺(PE)、磷脂酰丝氨酸(PS)、鞘磷脂(SM)、溶血磷脂酰胆碱(LPC)、磷脂酰肌醇(PI)、一种胆碱磷脂(CPLIP)和磷脂酰胆碱(PC)。利用各磷脂磷浓度的平均相对摩尔百分比差异来区分肿瘤。发现神经鞘瘤(神经鞘瘤、神经纤维瘤和纤维肉瘤)相对于神经胶质起源的肿瘤含有显著升高的SM水平,单独来看,多形性胶质母细胞瘤相对于神经鞘瘤、神经纤维瘤和脑膜瘤含有降低的SM水平。相对于神经鞘瘤,胶质母细胞瘤的PA水平显著降低,相对于脑膜瘤,PE水平也显著降低。相对于脑膜瘤,多形性胶质母细胞瘤中LPC和CPLIP水平升高。其他发现包括,相对于神经纤维瘤,多形性胶质母细胞瘤的PC水平升高,神经鞘瘤与神经纤维瘤的区别在于PA水平升高和PI水平降低。31P核磁共振磷脂分析提供了补充生化信息,可用于改善对体内获取光谱的解释,并揭示重要的肿瘤特异性生化信息,这可能进一步增进对颅内肿瘤生物学行为的理解。

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