Merchant T E, Kasimos J N, de Graaf P W, Minsky B D, Gierke L W, Glonek T
Department of Pathology, University Hospital Utrecht, The Netherlands.
Int J Colorectal Dis. 1991 May;6(2):121-6. doi: 10.1007/BF00300208.
Phospholipids of 16 malignant and 11 non-malignant human colon specimens were analyzed using a chloroform-methanol analytical reagent in conjunction with 31P magnetic resonance spectroscopy (MRS) at 202.4 MHz. Sixteen individual generic phospholipids were identified and quantified for statistical intergroup comparisons. Statistically significant elevations in the relative concentrations of lysophosphatidylcholine and phosphatidylcholine plasmalogen were seen in malignant tissues along with significantly depressed levels of sphingomyelin and phosphatidylethanolamine plasmalogen. The malignant and non-malignant tissue groups were further differentiated by the detection of the minor phospholipids, lysophosphatidylcholine plasmalogen, lysophosphatidylethanolamine plasmalogen, lysophosphatidic acid and phosphatidylglycerol exclusively present in the malignant tissues and by significant changes in computed phospholipid metabolic indices that were dominated by choline containing lipids. The 31P MRS methods used represent an advancement over previous protocols for identifying and quantifying major and minor tissue phospholipids making this the first direct study of membrane phospholipids in human colon tissues using 31P MRS. The phospholipid profiles obtained may provide important information regarding the nature of the malignant cell's membrane system and identify markers which may be used to estimate malignant propensity, aggressiveness of disease and provide prognostic information.
使用氯仿 - 甲醇分析试剂结合202.4 MHz的31P磁共振波谱(MRS)对16例恶性和11例非恶性人类结肠标本的磷脂进行了分析。鉴定并定量了16种个体通用磷脂,用于组间统计学比较。在恶性组织中观察到溶血磷脂酰胆碱和磷脂酰胆碱缩醛磷脂的相对浓度有统计学意义的升高,同时鞘磷脂和磷脂酰乙醇胺缩醛磷脂的水平显著降低。通过检测仅存在于恶性组织中的微量磷脂,即溶血磷脂酰胆碱缩醛磷脂、溶血磷脂酰乙醇胺缩醛磷脂、溶血磷脂酸和磷脂酰甘油,以及由含胆碱脂质主导的计算磷脂代谢指数的显著变化,进一步区分了恶性和非恶性组织组。所使用的31P MRS方法代表了在识别和定量主要和次要组织磷脂方面相对于先前方案的进步,这使得这成为首次使用31P MRS对人类结肠组织中的膜磷脂进行的直接研究。获得的磷脂谱可能提供有关恶性细胞膜系统性质的重要信息,并识别可用于估计恶性倾向、疾病侵袭性并提供预后信息的标志物。